Patent Abridgement 1 [3.1 MB PDF] - Intellectual Property Office of ...
Patent Abridgement 1 [3.1 MB PDF] - Intellectual Property Office of ...
Patent Abridgement 1 [3.1 MB PDF] - Intellectual Property Office of ...
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
Complete Specifications Accepted<br />
Copies <strong>of</strong> the specification and drawings (if any) can be obtained<br />
from the IPONZ website www.iponz.govt.nz.<br />
At any time within 3 months from the date <strong>of</strong> issue <strong>of</strong> this Journal, any<br />
person interested may give notice <strong>of</strong> opposition to the grant <strong>of</strong> a patent on<br />
any <strong>of</strong> the applications relating to the accepted complete specification<br />
shown hereunder, by filing form 15 in duplicate accompanied by a statement<br />
<strong>of</strong> the case in duplicate and a fee <strong>of</strong> $300 plus GST where applicable,<br />
provided that if an application for extension on form 16 is made within<br />
the said 3 months, the Commissioner may extend the prescribed period<br />
for opposition to 4 months from the date <strong>of</strong> issue <strong>of</strong> this Journal. The<br />
grounds for giving notice <strong>of</strong> opposition are specified in section 21 <strong>of</strong> the<br />
Act, and prospective opponents should also refer to regulations 48 to 56<br />
<strong>of</strong> the <strong>Patent</strong>s Regulations 1954.<br />
(21) 546609 (22) 23 Nov 2004<br />
(54) Resettable safety shield for medical needles<br />
(86) PCT/US2004/039400 (87) WO2005/053774<br />
(51) IPC2011.01:A61M5/00,32<br />
(71) Specialized Health Products, Inc.<br />
(72) Snow, Jeremy K; Ferguson, F Mark; Smith, Daniel K; Barrus, Roy L;<br />
Solomon, Donald D; Thorne, David L; Vanderstek, Bradley J;<br />
(31) 03 721526 (32) 25 Nov 2003 (33) US<br />
(31) 03 739868 (32) 18 Dec 2003 (33) US<br />
(31) 04 608565 (32) 10 Sep 2004 (33) US<br />
(31) 04 622392 (32) 27 Oct 2004 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) A medical needle shield apparatus is disclosed. The needle shield<br />
comprises: a needle hub (104) with a needle cannula (103) extending<br />
from there to a distal end; a retainer for releasable engagement with the<br />
needle hub (104), and at least one shield (101) which is extensible from<br />
a retracted position to an extended position to enclose a distal end <strong>of</strong> the<br />
needle. The shield (101) includes a binding member (105), which is disposed<br />
within the shield (101) and defines binding surfaces that form an<br />
aperture configured for slidable receipt <strong>of</strong> the needle between the retracted<br />
position and the extended position. The binding member (105)<br />
includes at least one drag inducing member so that the at least one drag<br />
inducing member engages the needle during slidable receipt <strong>of</strong> the needle<br />
to create a drag force with the needle. The drag force and shield<br />
facilitate rotation <strong>of</strong> the binding member (105) relative to a longitudinal<br />
axis <strong>of</strong> the needle so that the binding surfaces engage the needle to<br />
prevent slidable movement <strong>of</strong> the needle in the extended position <strong>of</strong> the<br />
shield. The binding member (105) further includes a needle communicating<br />
surface which extends from there so that the needle communicating<br />
surface can engage with the needle to prevent rotation <strong>of</strong> the binding<br />
member (105). The binding member (105) further includes a binding<br />
member reset surface (107) selectably alignable with a reset surface<br />
(108).<br />
(21) 546771 (22) 22 Oct 2004<br />
(54) A collet-type splice and dead end fitting for a composite core cable<br />
(86) PCT/US2004/035199 (87) WO2005/041358<br />
(51) IPC2011.01:H01R4/50,62,58<br />
(71) CTC CABLE CORPORATION<br />
(72) Bryant, David;<br />
(31) 03 690839 (32) 22 Oct 2003 (33) US<br />
(31) 04 911072 (32) 4 Aug 2004 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) A fitting for a cable having a composite core 101 comprising a collet<br />
304 comprised <strong>of</strong> one or more sections that form a truncated conical<br />
shape, the shape <strong>of</strong> the collet 304 comprising an outer diameter that<br />
increases from a first end to a second end creating an outside slope to<br />
slide within a collet housing 204, the collet further comprising a concentrically<br />
oriented lumen 214, the lumen 214 having a generally constant<br />
cross section along the length <strong>of</strong> the lumen 214 to fit a cross section and<br />
length <strong>of</strong> composite core 101, and a collet housing 204 having a first<br />
open end 226 to allow the collet 304 to fit into the collet housing 204 and<br />
a second open end 224 having a smaller internal diameter than the first<br />
open end, the housing 204 having a funnel-shaped interior that mirrors<br />
the outside slope <strong>of</strong> the collet 304 to enable the collet 304 to slide into the<br />
collet housing 204 through the first opening 226 without allowing the collet<br />
304 to be forcibly pulled 302 through the second open end <strong>of</strong> the<br />
collet housing 204.<br />
(21) 547673 (22) 23 Dec 2004<br />
(54) Use <strong>of</strong> substituted 2-aminotetralines for the preventative treatment <strong>of</strong><br />
parkinson’s disease<br />
(86) PCT/EP2004/014656 (87) WO2005/063238<br />
(51) IPC2011.01:A61K31/381,40,4164,404<br />
(71) UCB Pharma GmbH<br />
(72) Scheller, Dieter; Dressen, Frank;<br />
(31) 03 0361258 (32) 24 Dec 2003 (33) DE<br />
(74) DAVIES COLLISON CAVE - SYDNEY, 255 Elizabeth Street, Sydney,<br />
New South Wales 2000, Australia<br />
(57) Disclosed is the use <strong>of</strong> a tetralin tertiary amine compound <strong>of</strong> the general<br />
formula wherein, n = 1 to 5, R6 and R7 are independently alkyl or<br />
aryl, R5 is a alkyl and the further substituents are defined in the specification,<br />
wherein the compound <strong>of</strong> formula I is present as a racemate or as<br />
a pure (R)- or (S)-enantiomer as well as physiologically acceptable salts<br />
<strong>of</strong> these compounds, in the manufacture <strong>of</strong> a medicament or kit for the<br />
preventative treatment <strong>of</strong> Parkinson's disease.<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 53 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(21) 547754 (22) 3 Dec 2004<br />
(54) Packaging bag with a detachable gusset and a reclosable opening,<br />
and production machine and method<br />
(86) PCT/FR2004/003112 (87) WO2005/056405<br />
(51) IPC2011.01:B65D33/00,24,25; B65B61/18; B65D30/20; B65D85/16<br />
(71) S2F Flexico<br />
(72) Doue, Philippe;<br />
(31) 03 0314276 (32) 4 Dec 2003 (33) FR<br />
(74) Freehills <strong>Patent</strong> & Trade Mark Attorneys, Level 43, 101 Collins Street,<br />
Melbourne, Victoria 3000, Australia<br />
(57) A packaging bag 10 comprises at least one flap 24 formed at one end<br />
with the flap 24 folded back along a fold line 22 against a face <strong>of</strong> the bag<br />
body and held in this position by a detachable connecting element 32,<br />
and a recloseable closure element 50 which extends transversally to the<br />
fold line 22 along at least a substantial length <strong>of</strong> the bag body and along<br />
a full height <strong>of</strong> the flap 24.<br />
(21) 547841 (22) 23 Dec 2004<br />
(54) Use <strong>of</strong> rotigotine for the treatment or prevention <strong>of</strong> dopaminergic neurone<br />
loss<br />
(86) PCT/EP2004/014655 (87) WO2005/063237<br />
(51) IPC2011.01:A61K31/381<br />
(71) UCB Pharma GmbH<br />
(72) Scheller, Dieter; Dressen, Frank;<br />
(31) 03 0361259 (32) 24 Dec 2003 (33) DE<br />
(74) DAVIES COLLISON CAVE - SYDNEY, 255 Elizabeth Street, Sydney,<br />
New South Wales 2000, Australia<br />
(57) Provided is the use <strong>of</strong> rotigotine, or a salt or prodrug there<strong>of</strong>, for the<br />
manufacture <strong>of</strong> a medicament for the treatment or prophylaxis <strong>of</strong> a disease<br />
involving increased dopaminergic cell destruction, wherein the disease<br />
is selected from Parkinson's disease, an alphasynucleo-pathy,<br />
Huntington's disease, a REM sleep disturbance and an olfactory disorder,<br />
and wherein the treatment or prophylaxis is performed on individuals<br />
selected from: (a) individuals without symptoms <strong>of</strong> Parkinson's disease<br />
but with an increased risk <strong>of</strong> developing Parkinson's disease, and<br />
(b) individuals with early symptoms <strong>of</strong> Parkinson's disease, in whom at<br />
least three <strong>of</strong> the four cardinal symptoms <strong>of</strong> Parkinson's disease (rigidity,<br />
resting tremors, bradykinesia, postural instability) are not yet present,<br />
and wherein the prodrug is selected from the group consisting <strong>of</strong> esters,<br />
carbamates, acetals, ketals, phosphates, phosphonates, sulphates,<br />
sulphonates, silyl ethers, carbonates, acyloxyalkyl ethers, thiocarbonyl<br />
esters, oxythiocarbonyl esters, thiocarbamates and ethers.<br />
(21) 548257 (22) 28 Jan 2005<br />
(54) Modified human growth hormone polypeptides and their uses<br />
(86) PCT/US2005/002724 (87) WO2005/074546<br />
(51) IPC2011.01:C12P21/06<br />
(71) Ambrx, Inc.<br />
(72) Cho, Ho Sung; Daniel, Thomas; Dimarchi, Richard; Hays Putnam,<br />
Anna-Maria A.; Wilson, Troy; Litzinger, David; Sim, Bee-Cheng;<br />
(31) 04 581314 (32) 18 Jun 2004 (33) US<br />
(31) 04 581175 (32) 18 Jun 2004 (33) US<br />
(31) 04 541528 (32) 2 Feb 2004 (33) US<br />
(31) 04 580885 (32) 18 Jun 2004 (33) US<br />
(31) 04 638616 (32) 22 Dec 2004 (33) US<br />
(74) F B RICE & CO, Level 23, 44 Market Street, Sydney, New South<br />
Wales 2000, Australia<br />
(57) Disclosed is a human growth hormone (hGH) polypeptide comprising<br />
a non-naturally encoded amino acid (NEAA) comprising a carbonyl functional<br />
group, wherein said NEAA is positioned at a following position <strong>of</strong><br />
hGH comprising the amino acid sequence set forth in SEQ ID NO:2: (i)<br />
at the N-terminus; (ii) within residues 10-31; (iii) within residues 35-74;<br />
(iv) within residues 86-95; (v) within residues 97-102; (vi) within residues<br />
111-119; (vii) within residues 134-146; (viii) within residues 155-176; and<br />
(ix) at the C-terminus.<br />
Divisional filed as 590677<br />
(21) 548798 (22) 10 Feb 2005<br />
(54) Swinging agitator for a gypsum calcining apparatus and the like<br />
(86) PCT/US2005/004796 (87) WO2005/092583<br />
(51) IPC2011.01:B28C5/12; B01F11/00; B01F15/06; B01J6/00; C01F11/<br />
46; C04B11/028; F26B3/084,092<br />
(71) UNITED STATES GYPSUM COMPANY<br />
(72) Bolind, Michael L; Porter, Michael J;<br />
(31) 04 10788864 (32) 27 Feb 2004 (33) US<br />
(31) 04 10788871 (32) 27 Feb 2004 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) An agitation mechanism 60 for a gypsum processing apparatus 10<br />
which includes a housing 12 having a bottom wall 14, at least one side<br />
wall 18, and a support base 23 above and adjacent the bottom wall 14, a<br />
fluidization mechanism for introducing fluid to the gypsum based product,<br />
the fluidization mechanism defining at least a portion <strong>of</strong> the support<br />
base 23 <strong>of</strong> the housing 12, a burner conduit 28 extending through the<br />
housing 12 from at least one burner 22 and terminating through the support<br />
base 23 such that combustion gases from the burner 22 travel through<br />
the burner conduit 28 in the housing 12 and through the support base 23<br />
including the fluidization pad 54 back through the housing 12 and the<br />
gypsum based product, and an agitator frame 64 having a similarly shaped<br />
cross section to a cross section <strong>of</strong> the housing 12, the agitator frame 64<br />
pivotally connected internally to the housing 12 for reciprocating movement<br />
between first and second positions. The housing 12 is designed<br />
and constructed to receive and process powdered gypsum. The agitation<br />
mechanism 62 prevents the gypsum products from collecting adjacent<br />
to the bottom wall 14 <strong>of</strong> the housing 12.<br />
(21) 548823 (22) 16 Mar 2005<br />
(54) Galenic formulations <strong>of</strong> organic compounds (oral dosage <strong>of</strong> aliskiren)<br />
(86) PCT/EP2005/002798 (87) WO2005/089729<br />
(51) IPC2011.01:A61K31/00; A61K9/20,28<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 54 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(71) Novartis AG<br />
(72) Rigassi-Dietrich, Petra Gisela; Schmid, Martin;<br />
(31) 04 553878 (32) 17 Mar 2004 (33) US<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) Disclosed is a solid oral dosage form comprising; i) a therapeutically<br />
effective amount <strong>of</strong> aliskiren, or a pharmaceutically acceptable salt there<strong>of</strong>,<br />
as active ingredient in an amount <strong>of</strong> more than 46 percent by weight<br />
based on the total weight <strong>of</strong> the oral dosage form, wherein the oral dosage<br />
form is in the form <strong>of</strong> a tablet or film-coated tablet and is not obtained<br />
by wet granulation with excipients using water and/or an aqueous binder<br />
solution. Also disclosed is the use <strong>of</strong> said oral dosage form in the treatment<br />
<strong>of</strong> hypertension angina and stroke and a process to prepare said<br />
dosage form.<br />
(21) 549165 (22) 7 Jun 2004<br />
(54) Method for seed treatment with abamectin and thiamethoxam<br />
(86) PCT/EP2004/006109 (87) WO2005/094585<br />
(51) IPC2011.01:A01N25/00; A01N43/04,90; A01N51/00<br />
(71) Syngenta Participations AG<br />
(72) H<strong>of</strong>er, Dieter;<br />
(31) 04 553516 (32) 16 Mar 2004 (33) US<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) Disclosed is a method <strong>of</strong> protecting a plant against insects <strong>of</strong> the<br />
order Thysanoptera (thrips), which comprises treating plant propagation<br />
material there<strong>of</strong>, with (A) a nematicidally effective amount <strong>of</strong> a nematicide<br />
selected from abamectin, emamectin benzoate and spinosad and<br />
(B) at least one insecticidally effective amount <strong>of</strong> an insecticide selected<br />
from imidacloprid, clothianidin and thiamethoxam.<br />
(21) 549413 (22) 30 Mar 2005<br />
(54) Portable combustion driven fastener driving tool<br />
(86) PCT/IB2005/000823 (87) WO2005/095063<br />
(51) IPC2011.01:B25C1/00,06,08,18<br />
(71) JPF Works Co., Ltd.<br />
(72) Yamakawa, Keiji; Uejima, Yasutsugu;<br />
(31) 04 105992 (32) 31 Mar 2004 (33) JP<br />
(74) DAVIES COLLISON CAVE - MELBOURNE, 1 Nicholson Street, Melbourne,<br />
Victoria, Australia<br />
(57) A portable type fastener driving tool comprises a main body 1 which<br />
houses a rod 17 which drives in the fasteners n, a rod driving out means<br />
24 which pushes the rod 17 forward in the axial direction, a head part 3<br />
which is disposed on the front end <strong>of</strong> the main body 1 and which is provided<br />
with a fastener guiding part, a fastener retaining means which loads<br />
a fastener connecting body N which is made by connecting multiple<br />
fasteners n using a connecting material so that they are arranged parallel<br />
to one another, and a power operated fastener feed means which is<br />
loaded on the fastener retaining means, which feeds the fastener connecting<br />
bodies in the direction in which the fasteners n are arranged and<br />
which feeds the fasteners one by one in front <strong>of</strong> the rod 17. The fastener<br />
drive means is provided with a rotary type feed member which latches<br />
onto the fastener connecting bodies and feeds them, where the rod driving<br />
out means 24 uses combustion gas pressure as a source <strong>of</strong> motive<br />
force while the fastener feed means is provided with a feed gear which<br />
is used as a rotary type feed member, and an electric motor which drives<br />
this feed gear.<br />
(21) 550020 (22) 28 Feb 2005<br />
(54) A tissue retractor for treatment <strong>of</strong> a breathing disorder comprising a<br />
shaft, a retractor, and an anchor<br />
(86) PCT/US2005/006430 (87) WO2005/082452<br />
(51) IPC2011.01:A61N1/05<br />
(71) Linguaflex, LLC<br />
(72) Sanders, Ira;<br />
(31) 04 547897 (32) 26 Feb 2004 (33) US<br />
(74) DAVIES COLLISON CAVE - MELBOURNE, 1 Nicholson Street, Melbourne,<br />
Victoria, Australia<br />
(57) A tissue retractor for treatment <strong>of</strong> a breathing disorder, is disclosed.<br />
The tissue retractor comprises: a) a shaft sized for insertion into s<strong>of</strong>t<br />
tissue located in a patient's oral cavity or pharynx; b) a retractor member<br />
connected at or near a first end <strong>of</strong> the shaft; and c) an anchor member<br />
connected at or near a second end <strong>of</strong> the shaft. The retractor or anchor<br />
member is configured to be positioned on an external surface <strong>of</strong> the s<strong>of</strong>t<br />
tissue where the shaft, the retractor member or the anchor member is<br />
adapted to exert a force toward a center <strong>of</strong> the shaft between the first<br />
end and the second end <strong>of</strong> the shaft.<br />
Divisional filed as 589950<br />
(21) 550114 (22) 20 Apr 2005<br />
(54) Substituted thiazole and pyrimidine derivatives as melanocortin<br />
receptor modulators<br />
(86) PCT/US2005/013386 (87) WO2005/103022<br />
(51) IPC2011.01:C07D239/42; C07D277/42,46,52; C07D403/12;<br />
C07D409/12; C07D417/12,14; A61K31/426,427,506,505,428; A61P3/04<br />
(71) TRANSTECH PHARMA, INC.<br />
(72) Mjalli, Adnan M M; Gaddam, Bapu R; Qabaja, Ghassan; Subramanian,<br />
Govindan; Zhu, Jeff; Dankwardt, John; Arimilli, Murty N; Andrews, Robert<br />
C; Victory, Samuel; Tian, Ye E;<br />
(31) 04 563882 (32) 20 Apr 2004 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed is a thiazole compound <strong>of</strong> formula (Ib), or a pharmaceutically<br />
acceptable salt or solvate there<strong>of</strong>, wherein A is an amide or amine and<br />
where the rest <strong>of</strong> the substituents are disclosed within the specification.<br />
Also disclosed are pharmaceutical compositions comprising the said compound<br />
as well as further agents such as hypoglycaemic agents, agents<br />
that modulate thermogenesis, lipolysis, gut lotility, fat absorption, satiey<br />
and other such second agents.<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 55 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(21) 550124 (22) 28 Mar 2005<br />
(54) In-can fuel cell metering valve with a reduced number <strong>of</strong> seals<br />
(86) PCT/IB2005/051045 (87) WO2005/099968<br />
(51) IPC2011.01:B25C1/08; B65D83/14; F17C13/04<br />
(71) Illinois Tool Works Inc.<br />
(72) Vanstaan, Valery H; Wagdy, Mohamed K; Geier, Adalberto; Dalsant,<br />
Giuseppe;<br />
(31) 04 827551 (32) 19 Apr 2004 (33) US<br />
(74) DAVIES COLLISON CAVE - MELBOURNE, 1 Nicholson Street, Melbourne,<br />
Victoria, Australia<br />
(57) A fuel cell (10) for use with a combustion tool for delivery <strong>of</strong> a predetermined<br />
amount <strong>of</strong> fuel with each stem actuation is disclosed. The fuel<br />
cell (10) has a housing defining an open end enclosed by a closure (16).<br />
A main valve stem (26) has an outlet (28) which moves relative to the<br />
housing between a closed position wherein the stem (26) is extended,<br />
and an open position wherein the stem (26) is retracted. A fuel metering<br />
valve (25) is located within the housing and includes a fuel metering<br />
chamber (38) in close proximity to the closure (16). The fuel metering<br />
chamber (38) is configured so that when the stem (26) is in the open<br />
position, only a measured amount <strong>of</strong> fuel is dispensed through the outlet<br />
(28). In a preferred embodiment, the fuel cell housing includes a separate<br />
fuel container (22), and the fuel metering valve (25) includes a valve<br />
body (34) with a second end (64) opposite the fuel metering chamber<br />
(38) located within the container.<br />
(21) 550348 (22) 8 Apr 2005<br />
(54) Nasal assembly with vent and baffle<br />
(86) PCT/AU2005/000515 (87) WO2005/097247<br />
(51) IPC2011.01:A61M16/06; A61M15/08; A62B7/00; A61M16/08<br />
(71) ResMed Ltd<br />
(72) Gunaratnam, Michael Kassipillai; Kwok, Philip Rodney; Hitchcock,<br />
Robin Garth; Veliss, Lee James; Guney, Memduh; Sokolov, Richard;<br />
Lithgow, Perry David; Darkin, Donald; Lynch, Susan Robyn;<br />
Dantanarayana, Muditha; Moore, Rachel;<br />
(31) 04 560610 (32) 9 Apr 2004(33) US<br />
(31) 04 632193 (32) 2 Dec 2004 (33) US<br />
(74) JAMES & WELLS, Level 12, KPMG Centre, 85 Alexandra Street,<br />
Hamilton, New Zealand<br />
(57) A nasal assembly 50 for delivering breathable gas to a patient, comprises<br />
a frame having a main body, a patient interface provided to the<br />
main body <strong>of</strong> the frame and defining a plenum chamber, the patient interface<br />
adapted to sealingly engage with a patient, at least one vent 52 to<br />
provide a vent exit for the passage <strong>of</strong> exhaled gas, and a baffle (not<br />
shown) provided to the frame, the baffle including at least one arm adapted<br />
to extend into the plenum chamber <strong>of</strong> the patient interface and at least<br />
partially separate the vent exit from an air inlet.<br />
Divisional filed as 586208<br />
(21) 550571 (22) 18 Apr 2005<br />
(54) 3-THIOCARBAMOYLPYRAZOLE DERIVATIVES AS PESTICIDES<br />
(86) PCT/US2005/013097 (87) WO2005/099453<br />
(51) IPC2011.01:A01N43/56; A61K31/415,416; C07D231/18,38,44;<br />
C07D403/04; C07D231/14<br />
(71) Merial Ltd<br />
(72) Soll, Mark D; Boeckh, Albert; Kumar, Krishan; Shub, Natalya;<br />
(31) 04 826105 (32) 16 Apr 2004 (33) US<br />
(74) F B RICE & CO, Level 23, 200 Queen Street, Melbourne, Victoria<br />
3000, Australia<br />
(57) A process for the control or elimination <strong>of</strong> external parasites from an<br />
animal is disclosed, which comprises: topically applying in a localized<br />
region on the back <strong>of</strong> the animal at a dose <strong>of</strong> between about 1 to 50 mg/<br />
kg a spot-on formulation comprising a compound <strong>of</strong> the formula (II), and<br />
subjecting the applied formulation to degradation by exposing it to a sufficient<br />
amount <strong>of</strong> U.V. light or fluorescent light to convert the compound<br />
<strong>of</strong> formula (II) to the corresponding 3-cyano derivative in an amount sufficient<br />
to control external parasites while diffusing therefrom over the<br />
animal’s body and/or in the sebaceous glands <strong>of</strong> the animal and thereby<br />
obtaining said control or elimination <strong>of</strong> said external parasites,<br />
wherein R1 represents H2N"CS"; and the other variables shown in the<br />
structural formula (II) are as defined in the specification. A process for<br />
preparing the corresponding 3-cyano derivative <strong>of</strong> the compound <strong>of</strong> formula<br />
(II) is also disclosed, which comprises degrading a compound <strong>of</strong><br />
the formula (II) in the presence <strong>of</strong> U.V. light, fluorescent light or heat.<br />
(21) 550894 (22) 6 May 2005<br />
(54) Solid dosage form <strong>of</strong> wetted heparin<br />
(86) PCT/US2005/016012 (87) WO2005/107773<br />
(51) IPC2011.01:A61K31/727; C07C229/36; C07C233/83; C08L5/10;<br />
A61K31/166<br />
(71) Emisphere Technologies, Inc.<br />
(72) Majuru, Shingai; Singh, Brahma; Dhoot, Nikhil;<br />
(31) 04 569475 (32) 6 May 2004 (33) US<br />
(31) 04 572679 (32) 19 May 2004 (33) US<br />
(31) 04 598978 (32) 4 Aug 2004 (33) US<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 56 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(57) Disclosed is a solid pharmaceutical composition comprising: (a) a<br />
delivery agent <strong>of</strong> formula (I) wherein; R1, R2, R3 and R4 are independently<br />
hydrogen, hydroxy, -NR6R7, halogen, alkyl, or alkoxy; R5 is a substituted<br />
or unsubstituted alkylene, a substituted or unsubstituted<br />
alkenylene, a substituted or unsubstituted alkyl(arylene), or a substituted<br />
or unsubstituted aryl(alkylene); and R6 and R7 are independently hydrogen,<br />
oxygen, or alkyl; and (b) wetted heparin. Also disclosed is the use<br />
<strong>of</strong> an anti-thrombosis effective amount <strong>of</strong> the solid pharmaceutical composition<br />
as defined above for the manufacture <strong>of</strong> a medicament for treating<br />
or preventing thrombosis in an animal. Of particular importance are<br />
the compositions where the delivery agent is monosodium N-[8-(2hydroxybenzoyl)amino]caprylate<br />
(SNAC).<br />
(21) 550909 (22) 10 May 2005<br />
(54) Glycopyrrolate for treating childhood asthma<br />
(86) PCT/GB2005/001791 (87) WO2005/107873<br />
(51) IPC2011.01:A61K31/00,352,40,439,465; A61P11/06; A61K9/14<br />
(71) SOSEI R&D LTD.<br />
(72) Snape, Susan; Bannister, Robin Mark;<br />
(31) 04 0410399 (32) 10 May 2004 (33) GB<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed is the use <strong>of</strong> glycopyrrolate for the manufacture <strong>of</strong> a medicament<br />
which is a dry powder composition for pulmonary delivery, comprising<br />
microparticles <strong>of</strong> glycopyrrolate, for the treatment <strong>of</strong> asthma in a<br />
child aged 2 to 12 years, with the proviso that said treatment excludes<br />
the treatment <strong>of</strong> bronchospasms.<br />
(21) 550942 (22) 4 May 2005<br />
(54) Directly compressible tricalcium phosphate<br />
(86) PCT/US2005/015385 (87) WO2005/107722<br />
(51) IPC2011.01:A61K33/42,06; A61K9/14,16,20,30,32,34<br />
(71) Innophos, Inc.<br />
(72) Hendricks, Lewis Roe; Jobbins, Jill Marie; Camarco, Wayne;<br />
(31) 04 567926 (32) 4 May 2004 (33) US<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) Disclosed is a compressible tricalcium phosphate agglomerate, comprising,<br />
based on 100 parts by weight (pbw) <strong>of</strong> the agglomerate, from<br />
about 90 to about 99 pbw tricalcium phosphate particles, each having an<br />
outer surface, and from about 1 to about 10 pbw <strong>of</strong> a binder comprising<br />
a polyvinylpyrrolidone (PVP), carageenan, a guar gum, a modified guar<br />
gum, or a mixture <strong>of</strong> a guar gum and a modified guar gum supported on<br />
at least a portion <strong>of</strong> the outer surface <strong>of</strong> at least a portion <strong>of</strong> the tricalcium<br />
phosphate particles and made by spray drying an aqueous slurry comprising<br />
the tricalcium phosphate particles and the binder. Also disclosed<br />
is a process for making an oral dosage form <strong>of</strong> the agglomerate and the<br />
instance where the oral dosage form is a chewable calcium dietary supplement.<br />
(21) 550985 (22) 20 May 2005<br />
(54) Cyclic amide derivatives, and their production and use as<br />
antithrombotic agents<br />
(86) PCT/JP2005/009711 (87) WO2005/113504<br />
(51) IPC2011.01:A61K31/45,506,5377; A61P7/02; C07D211/76; C07D401/<br />
04; C07D403/04; C07D413/04; C07D417/04<br />
(71) Takeda Pharmaceutical Company Limited<br />
(72) Kubo, Keiji; Imaeda, Yasuhiro;<br />
(31) 04 152000 (32) 21 May 2004 (33) JP<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) Disclosed is a cyclic amide derivative which inhibits activated blood<br />
coagulation factor X (FXa) to exhibit anticoagulant activity and<br />
antithrombotic activity. The compound is useful as a drug for treating<br />
thrombosis, and is represented by the formula (I): wherein R1 represents<br />
a naphthyl which may be substituted with a halogen atom, W represents<br />
a bond, a represents 0, 1, or 2, X1 represents a C1-6 alkylene<br />
which may be substituted with a hydroxy group, Y1 represents –C(O)-, A<br />
represents a piperazine ring or a piperidine ring, and the remaining<br />
substituents are as defined in the specification.<br />
(21) 551420 (22) 10 May 2005<br />
(54) Method <strong>of</strong> screening candidate compounds for susceptibility to biliary<br />
excretion in hepatocyte cell cultures<br />
(86) PCT/US2005/016240 (87) WO2005/118787<br />
(51) IPC2011.01:C12N5/08; C12Q1/00<br />
(71) The University <strong>of</strong> North Carolina at Chapel Hill<br />
(72) Brouwer, Kim L; Tian, Xianbin; Zhang, Peijin;<br />
(31) 04842404 (32) 10 May 2004 (33) US<br />
(74) JAMES & WELLS, Level 12, KPMG Centre, 85 Alexandra Street,<br />
Hamilton, New Zealand<br />
(57) A method <strong>of</strong> screening a candidate compound for susceptibility to<br />
biliary excretion by a hepatocyte transport protein, the method comprising:<br />
(a) providing a cell culture comprising a plurality <strong>of</strong> hepatocytes and at<br />
least one bile canaliculus, at least one <strong>of</strong> the hepatocytes comprising a<br />
transport protein;<br />
(b) exposing a candidate compound to the culture; and<br />
(c) determining an amount <strong>of</strong> the candidate compound in the at least one<br />
bile canaliculus to thereby screen the candidate compound for susceptibility<br />
to biliary excretion by the hepatocyte transport protein, comprising<br />
inhibiting expression <strong>of</strong> the hepatocyte transport protein and detecting<br />
an amount <strong>of</strong> the candidate compound present in the at least one bile<br />
canaliculus, wherein the presence <strong>of</strong> a reduced amount <strong>of</strong> the candidate<br />
compound in the at least one bile canaliculus as compared to an amount<br />
<strong>of</strong> the candidate compound in the at least one bile canaliculus when<br />
expression <strong>of</strong> the hepatocyte transport protein is not inhibited indicates<br />
the susceptibility <strong>of</strong> the candidate compound to biliary excretion by the<br />
hepatocyte transport protein.<br />
Divisional filed as 586465<br />
(21) 551448 (22) 20 May 2005<br />
(54) Analysis <strong>of</strong> liquid chromotography eluates<br />
(86) PCT/IB2005/001772 (87) WO05/114171<br />
(51) IPC2011.01:G01N30/64,74,78<br />
(71) Novartis Vaccines and Diagnostics S.r.l.<br />
(72) Proietti, Daniela; Bardotti, Angela; Ricci, Stefano;<br />
(31) 04 0411283 (32) 20 May 2004 (33) GB<br />
(31) 04 0420649 (32) 16 Sep 2004 (33) GB<br />
(74) F B RICE & CO, Level 23, 44 Market Street, Sydney, New South<br />
Wales 2000, Australia<br />
(57) Disclosed is a method for detecting the presence <strong>of</strong> one or more<br />
saccharide analytes in a sample, said method comprising applying the<br />
sample to an anion exchange chromatography column under conditions<br />
wherein one or more saccharide analytes bind to the column, applying<br />
an elution buffer comprising an anion selected from a nitrate, a carbonate<br />
and a borate to thereby elute one or more saccharide analytes from<br />
the column, and analysing the eluate by both amperometry and<br />
spectroscopy. Also disclosed is apparatus when used to analyse a sample<br />
comprising one or more saccharide analytes, wherein the apparatus<br />
comprises (i) an anion exchange chromatography column, (ii) an elution<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 57 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
buffer comprising an anion selected from a nitrate, a carbonate and a<br />
borate, (iii) an amperometric detector and (iv) a spectroscopic detector,<br />
wherein the two detectors are arranged to receive an eluate comprising<br />
one or more saccharide analytes in the elution buffer from the column.<br />
(21) 551715 (22) 15 Jun 2005<br />
(54) Single piece, gussetted cushion for a respiratory mask assembly<br />
(86) PCT/AU2005/000850 (87) WO2005/123166<br />
(51) IPC2011.01:A61M16/06<br />
(71) ResMed Limited<br />
(72) FRATER, Robert Henry; DREW, Joanne Elizabeth; KWOK, Philip<br />
Rodney; MCAULIFFE, Patrick John; DAVIDSON, Aaron Samuel;<br />
HITCHCOCK, Robin Garth; GUNARATNAM, Michael Kassipillai;<br />
(31) 04 579678 (32) 16 Jun 2004 (33) US<br />
(31) 04 634272 (32) 9 Dec 2004 (33) US<br />
(31) 05 648687 (32) 2 Feb 2005 (33) US<br />
(74) JAMES & WELLS, Level 12, KPMG Centre, 85 Alexandra Street,<br />
Hamilton, New Zealand<br />
(57) A mask assembly 10 comprises a frame 12, an elastomeric, onepiece<br />
cushion provided to the frame 12 with the cushion including a breathing<br />
chamber forming portion and a face contacting portion with the breathing<br />
chamber forming portion defining a mask interior breathing chamber<br />
and the face contacting portion structured to engage a patient's face,<br />
and a tubular connector 22 supported by the frame 12 and adapted to<br />
connect to an air delivery conduit. Flexibility is provided to the face contacting<br />
portion <strong>of</strong> the cushion by a gusseted portion including one or<br />
more folds.<br />
Divisional filed as 587820<br />
(21) 552230 (22) 30 Jun 2005<br />
(54) Systems and methods for controlling spooling <strong>of</strong> linear material including<br />
a motor and controller<br />
(86) PCT/US2005/023652 (87) WO06/007582<br />
(51) IPC2011.01:B65H75/34<br />
(71) GREAT STUFF, INC.<br />
(72) Lee, Michael J; Tracey, James B A; Koebler, Martin; Caamano, Ramon<br />
Anthony;<br />
(31) 04 584797 (32) 1 Jul 2004 (33) US<br />
(31) 04 585042 (32) 2 Jul 2004 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) An automatic reel for facilitating the spooling <strong>of</strong> linear material is disclosed.<br />
The automatic reel includes a rotatable member, a motor, and a<br />
motor controller. The rotatable member has a spool surface and is capable<br />
<strong>of</strong> winding a linear material around the spool surface as the rotatable<br />
member rotates in a first direction. The rotatable member is also capable<br />
<strong>of</strong> deploying the linear material from around the spool surface as the<br />
rotatable member rotates in a second direction. The motor is capable <strong>of</strong><br />
interacting with the rotatable member to selectively rotate the rotatable<br />
member in the first direction or in the second direction. The motor controller<br />
is capable <strong>of</strong> sensing a parameter associated with the motor and<br />
indicative <strong>of</strong> a tension <strong>of</strong> the linear material. The motor controller is capable<br />
<strong>of</strong> outputting a control signal to cause the motor to rotate the rotatable<br />
member in the second direction to deploy the linear material when<br />
the sensed parameter indicates that the tension <strong>of</strong> the linear material<br />
exceeds a certain amount.<br />
(21) 552452 (22) 6 Jul 2005<br />
(54) A method for preparing an echinacea formulation from a combination<br />
<strong>of</strong> Echinacea angustifolia and Echinacea purpurea<br />
(86) PCT/AU2005/000993 (87) WO2006/002493<br />
(51) IPC2011.01:A61P37/04; A61K36/00<br />
(71) MediHerb Holdings Ltd<br />
(72) Lehmann, Reg; Bone, Kerry; Penman, Kerry; Matthias, Anita;<br />
(31) 04 903716 (32) 7 Jul 2004 (33) AU<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) Disclosed is a method for preparing an Echinacea formulation which<br />
includes a combination <strong>of</strong> Echinacea angustifolia and Echinacea<br />
purpurea, the method including the step <strong>of</strong> adding sufficient Echinacea<br />
angustifolia to the Echinacea purpurea such that the weight ratio <strong>of</strong> 2ene<br />
alkylamide to 2,4-diene alkylamide in the formulation is between about<br />
1:15 to about 2:1.<br />
Divisional filed as 589801<br />
(21) 552600 (22) 13 Jul 2005<br />
(54) A gas burner with two gas flow passages<br />
(86) PCT/NZ2005/000172 (87) WO2006/006882<br />
(51) IPC2011.01:F23D14/02<br />
(71) FISHER & PAYKEL APPLIANCES LIMITED<br />
(72) Graham, Lindsay George; Brown, Simon Denzil;<br />
(31) 04 534091 (32) 13 Jul 2004 (33) NZ<br />
(31) 04 621001 (32) 21 Oct 2004 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) A gas burner comprises a first gases flow passage 52 with an inlet<br />
and an outlet, a source <strong>of</strong> oxidising gases at the inlet <strong>of</strong> the first passage<br />
52, a second gases flow passage with an inlet and an outlet, a source <strong>of</strong><br />
oxidising gases at the inlet <strong>of</strong> the second passage, the outlet <strong>of</strong> the first<br />
passage 52 proximate to the outlet second passage, a fuel gas jet 46<br />
configured to supply fuel to the second passage, a flame locating means<br />
49 within the second passage 52 sheltered from the oxidising gases in<br />
the first passage 52, and a burner cap 3 spaced downstream from the<br />
outlet <strong>of</strong> the second flow passage. The burner cap 3 extends transversely<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 58 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
to the outlet <strong>of</strong> the second flow passage. Oxidising gas is typically supplied<br />
by fan 41 and flows over baffle 54 to the first passage 52 via circumferentially<br />
spaced slots in the burner housing.<br />
(21) 552803 (22) 8 Jul 2005<br />
(54) (1S,5S)-3-(5,6-dichloropyridin-3-YL)-3,6-diazabicyclo[3.2.0]heptane<br />
benzenesulfonate<br />
(86) PCT/US2005/024464 (87) WO2006/019668<br />
(51) IPC2011.01:C07D487/04<br />
(71) ABBOTT LABORATORIES<br />
(72) Wayne, Greg S; Mellican, Sean M; Zhang, Ge<strong>of</strong>f G; Willcox, David R;<br />
Breting, Jeffrey M;<br />
(31) 04 590677 (32) 23 Jul 2004 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed is a crystalline (1S,5S)-3-(5,6-dichloropyridin-3-yl)-3,6diazabicyclo[3.2.0]heptane<br />
benzenesulfonate demonstrating at least one<br />
characteristic peak in the powder X-ray diffraction pattern at values <strong>of</strong><br />
two theta <strong>of</strong> 8.8 +/- 0.2, 11.8, 13.7, 15.1, 17.2, 18.5, 18.9, 20.6, 24.4,<br />
24.7, and 27.4 +/-0.2,<br />
Also disclosed is amorphous (1S,5S)-3-(5,6-dichloropyridin-3-yl)-3,6<br />
diazabicyclo [3.2.0]heptane benzenesulfonate.<br />
(21) 552898 (22) 28 Jul 2005<br />
(54) Method <strong>of</strong> producing a composition, composition and its use<br />
(86) PCT/NO2005/000281 (87) WO2006/011809<br />
(51) IPC2011.01:A61B5/055; A61K49/06,10; C07B61/02; C07D519/00<br />
(71) GE HEALTHCARE AS<br />
(72) Thaning, Mikkel;<br />
(31) 04 043229 (32) 30 Jul 2004 (33) NO<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) The disclosure relates to a method for producing a liquid composition<br />
comprising hyperpolarised 13C-pyruvate said method comprising:<br />
(a) forming a liquid mixture comprising a radical <strong>of</strong> formula (I), 13C-pyruvic<br />
acid and/or 13C-pyruvate and freezing the mixture;<br />
(b) enhancing the 13C nuclear polarisation <strong>of</strong> pyruvic acid and/or pyruvate<br />
in the mixture via DNP;<br />
(c) adding a buffer and a base to the frozen mixture to dissolve it and to<br />
convert the 13C-pyruvic acid into a 13C-pyruvate to obtain a liquid composition<br />
or, when only 13C-pyruvate is used in step (a), adding a buffer<br />
to the frozen mixture to dissolve it to obtain a liquid composition; and<br />
(d) optionally removing the radical and/or reaction products there<strong>of</strong> from<br />
the liquid composition. The comprising hyperpolarised 13C-pyruvate<br />
composition produced by this method is suitable for use as an imaging<br />
agent for in vivo MR imaging <strong>of</strong> a human or non-human animal body.<br />
(21) 552941 (22) 25 Jul 2005<br />
(54) Modification <strong>of</strong> the lignin biosynthesis gene hydroxycinnamoyl transferase<br />
(HCT)<br />
(86) PCT/US2005/026253 (87) WO2006/012594<br />
(51) IPC2011.01:A01H5/00,10; C12N15/82<br />
(71) The Samuel Roberts Noble Foundation, Inc.<br />
(72) Dixon, Richard A; Reddy, M S Srinivasa; Chen, Fang;<br />
(31) 04 590991 (32) 24 Jul 2004 (33) US<br />
(74) Pizzeys <strong>Patent</strong> and Trade Mark Attorneys, Level 14, ANZ Centre, 324<br />
Queen Street, Brisbane, Queensland 4000, Australia<br />
(57) Disclosed is a transgenic plant comprising a selected DNA, wherein<br />
the selected DNA down regulates the lignin biosynthesis gene<br />
hydroxycinnamoyl transferase (HCT), said selected DNA comprising at<br />
least 18 contiguous nucleotides <strong>of</strong> the HCT gene or its complement, and<br />
wherein said plant is a legume.<br />
Divisional filed as 589209<br />
(21) 552953 (22) 8 Aug 2005<br />
(54) Medical skin applicator apparatus with an internal fluid container, a<br />
penetrating member and actuated by an externally protruding member<br />
(86) PCT/US2005/028162 (87) WO2007/018541<br />
(51) IPC2011.01:A61M5/00<br />
(71) TYCO HEALTHCARE GROUP, LP<br />
(72) CABLE, Frank; TAUER, Mark; FETTERROLL, Andrew;<br />
(31) 60 599927 (32) 9 Aug 2004 (33) US<br />
(31) 60 614503 (32) 30 Sep 2004 (33) US<br />
(31) 60 639182 (32) 22 Dec 2004 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) A medical skin applicator apparatus comprises an outer housing 534<br />
defining a longitudinal axis, a fluid housing 506 having a fluid chamber<br />
for storing a medical agent, a manually engagable member 530 connected<br />
to the fluid housing 506 and extending beyond the outer housing<br />
534, and an applicator 504 coupled to the housing 534. The manually<br />
engagable member can be depressed to cause longitudinal movement<br />
<strong>of</strong> the fluid housing 506 to the actuated position. The fluid housing 506<br />
has a cap 508 with a penetrable wall to permit access to the fluid chamber<br />
and release <strong>of</strong> the medical agent. The applicator 504 includes an<br />
applicator frame and an applicator surface for applying the medical agent<br />
to a patient. The applicator frame has an internal penetrating member<br />
558 adapted to penetrate the penetrable wall <strong>of</strong> the fluid housing cap<br />
upon achieving a predetermined coupled relation <strong>of</strong> the fluid housing<br />
506 and the applicator 504, to thereby permit the medical agent to be<br />
dispensed from the fluid chamber and applied to the patient with the<br />
applicator surface.<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 59 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(21) 553028 (22) 27 Jul 2005<br />
(54) Isoindoline compounds and methods <strong>of</strong> making and using the same<br />
(86) PCT/US2005/026680 (87) WO2006/025991<br />
(51) IPC2011.01:A61K31/4035; A61P11/00; A61P29/00; A61P35/00;<br />
C07D209/46,48<br />
(71) CELGENE CORPORATION<br />
(72) Muller, George W; Man, Hon-Wah;<br />
(31) 04 900270 (32) 28 Jul 2004 (33) US<br />
(74) HENRY HUGHES, 119-125 Willis Street, Wellington, New Zealand<br />
(57) Disclosed is a N-benzyl isoindoline derivative, or pharmaceutically<br />
acceptable salt, solvate, stereoisomer or prodrug there<strong>of</strong>, as defined in<br />
the specification in particular, 3-(1,3-dioxobenzo[e]isoindolin-2-yl)-3-(-3ethoxy-4-methoxyphenyl)propanenitrile,<br />
(1S)-Furan-2-carboxylic acid {2-<br />
[1-(3-ethoxy-4-methoxyphenyl)-2-methanesulfonyl-ethyl]-1,3-dioxo-2,3dihydro-1H-isoindol-4-yl}-amide,<br />
(1S)-N-{2-[1-(3-ethoxy-4-methoxyphenyl)-<br />
2- methanesulfonyl-ethyl]-l ,3-dioxo-2,3-dihydro-lHisoindol-4-yl}-2methoxy-acetamide,(1S)-7-(cyclopropylmethyl-amino)-2-[1-(3-ethoxy-4methoxyphenyl)-2-methanesulfonyl-ethyl]-2,3-dihydro-isoindol-l-one,(1S)-2-[1-(3-Ethoxy-4-methoxyphenyl)-2methanesulfonyl-ethyl]-7isobutylamino-2,3-dihydro-isoindol-1-one,(3R)-3-[7-(2,2-simethylpropylamino)-1-oxo-1,3-dihydro-isoindol-2-yl]-3-(3-ethoxy-<br />
4methoxyphenyl)-N,N-dimethyl-propionamide, 3-(3-ethoxy-4-methoxyphenyl)-3-(4-isobutylamino1,3-dioxo-l,3-dihydro-isoindol-2-yl)propionitrile,N-{2-[cyano(3-ethoxy-4-methoxyphenyl)methyl]-1,3dioxoisoindolin-4-yl}acetamide,N-{2-[Cyano(3-ethoxy-4metboxyphenyl)methyl]1,3-dioxoisoindolin-4yl}(benzylamino)carboxamide,N-{2-[cyano(3-cyclopentyloxy-4methoxyphenyl)methyl]-1,3-dioxoisoindolin-4-yl}acetamide,<br />
amino-N-{2-<br />
[cyano(3-ethoxy-4-methoxyphenyl)methyl]-1,3-dioxoisoindolin-5yl}amide,<br />
amino-N-{2-[cyano(3-ethoxy-4methoxyphenyl)-methyl]-1,3dioxoisoindolin-4yl}amide,N-{2-[1-(3-cyclopropylmethoxy-4methoxyphenyl)-2-methanesulfonyl-ethyl]-1,3-dioxo-2,3-dihydro-1Hisoindol-4-yl}-acetamide,<br />
cyclopropanecarboxylic acid {2-[1-(3cyclopropylmethoxy-4-methoxy-phenyl)-2-methanesulfonyl-ethyl]-3-oxo-<br />
2,3-dihydro-1H-isoindol-4-yl}-amide, (3R)-3(7-(3,3-dimethyl-ureido)-1oxo-1,3-dihydro-isoindol-2-yl}-3-(3-ethoxy-4-methoxy-phenyl)-N,Ndimethylpropionamide<br />
and (1S)-3-{2-[1-(3-ethoxy-4-methoxy-phenyl)-2methanesulfonyl-ethyl]-3-oxo-2,3-dihydro-1H-isoindol-4-yl}-1,1-dimethylurea<br />
wherein the pictured compounds are representative examples. Also<br />
disclosed is the use <strong>of</strong> the above compound for treating disorders affecting<br />
by PDE4 inhibition or the production <strong>of</strong> TNF-alpha e.g. cancer, depression<br />
and arthritis.<br />
(21) 553258 (22) 17 Aug 2005<br />
(54) 5-[3-(4-Benzyloxyphenylthio)-fur-2-yl]-imidazolidin-2,4-dione and analogues<br />
as inhibitors <strong>of</strong> macrophage elastase<br />
(86) PCT/US2005/029259 (87) WO2006/023562<br />
(51) IPC2011.01:A61K31/4166; C07D405/04; A61P11/06; C07D233/76,78;<br />
C07D307/64; A61K31/341<br />
(71) QUEST PHARMACEUTICAL SERVICES (QPS)<br />
(72) Yang, Fude;<br />
(31) 04 602736 (32) 19 Aug 2004 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed are hydantoin derivatives <strong>of</strong> formula (IV) (such as 5-[3-(4benzyloxyphenylthio)furan-2-yl]imidazoline-2,4-dione)<br />
and their<br />
pharmaceutically acceptable salts, wherein R is selected from the group<br />
consisting <strong>of</strong> phenyl, 4-benzyloxyphenyl, 4-biphenyl, 4-methoxyphenyl,<br />
3-methoxyphenyl, 2-methoxyphenyl, 3,5-dimethoxyphenyl, 4chlorophenyl,<br />
3-chlorophenyl, 2-chlorophenyl, 4-methylphenyl, 3methylphenyl,<br />
2-methylphenyl, and 3-trifluoromethylphenyl. Also disclosed<br />
is the use <strong>of</strong> a compound as defined above in the manufacture <strong>of</strong> a<br />
medicament to treat a disease or disorder responsive to inhibition <strong>of</strong><br />
MMP-12 in a patient in need there<strong>of</strong> (and particularly conditions such as<br />
asthma, chronic obstructive pulmonary disease (COPD), arthritis, cancer,<br />
heart disease or nephritis).<br />
(21) 553320 (22) 26 Aug 2005<br />
(54) Ceramide derivatives as modulators <strong>of</strong> immunity and autoimmunity<br />
(86) PCT/US2005/030330 (87) WO2006/026389<br />
(51) IPC2011.01:A61K31/7028,715; C12N5/08<br />
(71) Albert Einstein College <strong>of</strong> Medicine<br />
(72) Porcelli, Steven A;<br />
(31) 04 605362 (32) 27 Aug 2004 (33) US<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) Disclosed are alpha-galactosylceramides and glycosylceramides<br />
("ceramide-like glycolipids") that modulate NK T cells. The ceramide-like<br />
glycolipids vary in the cytokines induced in NK T cells and vary in the<br />
antigen-presenting cells that are capable <strong>of</strong> efficiently presenting the<br />
compounds to NK T cells. Pharmaceutical compositions <strong>of</strong> the ceramidelike<br />
glycolipids are provided, as are pharmaceutical compositions <strong>of</strong> the<br />
ceramide-like glycolipids combined with dendritic cells. Methods utilizing<br />
the ceramide-like glycolipids in vaccines, to activate NK T cells, to stimulate<br />
the immune system, and to treat mammals are also provided. The<br />
disclosure also provides methods <strong>of</strong> evaluating a compound for its ability<br />
to activate an NK T cell in the presence <strong>of</strong> a cell expressing a CD 1 d<br />
protein.<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 60 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(21) 553384 (22) 14 Sep 2005<br />
(54) Peptide-based diagnostic compounds useful for diagnostic imaging<br />
using positron emission tomography (PET) and preparations there<strong>of</strong><br />
(86) PCT/IB2005/002727 (87) WO2006/030291<br />
(51) IPC2011.01:A61K51/08<br />
(71) GE HEALTHCARE AS; GE HEALTHCARE LIMITED<br />
(72) Solbakken, Magne; Arbo, Bente; Cuthbertson, Alan; Gibson, Alexander;<br />
(31) 04 20344 (32) 14 Sep 2004 (33) GB<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed herein is a method for radi<strong>of</strong>luorination comprising reaction<br />
<strong>of</strong> a compound <strong>of</strong> formula (I) with a compound <strong>of</strong> formula (II) to give<br />
a compound <strong>of</strong> formula (III), wherein the substituents are as defined<br />
within the specification. The peptide-based compounds are useful for<br />
diagnostic imaging using positron emission tomography (PET). More<br />
specifically said compounds are useful for targeting vectors that bind to<br />
receptors associated with angiogenesis, in particular integrin receptors<br />
(the ávâ3 integrin receptor).<br />
(21) 553774 (22) 17 Aug 2005<br />
(54) A teatcup, and a teatcup part<br />
(86) PCT/SE2005/001219 (87) WO06/031164<br />
(51) IPC2011.01:A01J5/08<br />
(71) DELAVAL HOLDING AB<br />
(72) Mehinovic, Raza; Petterson, Torbjorn;<br />
(31) 04 0402203 (32) 14 Sep 2004 (33) SE<br />
(74) HENRY HUGHES, 119-125 Willis Street, Wellington, New Zealand<br />
(57) A teatcup adapted to be attached to a teat <strong>of</strong> an animal to be milked is<br />
disclosed. The teatcup includes a teatcup part (1) and a connection part<br />
(2). The teatcup part is disengageably mountable to the connection part.<br />
The teatcup part includes a shell (3) and a teatcup liner (4) having an<br />
upper opening and a lower opening. The teatcup liner forms an inner<br />
space (12) for receiving the teat through the upper opening and being<br />
provided in the shell in such a way that a pulsation chamber (12) is formed<br />
between the teatcup liner and the shell. The connection part including a<br />
milk-discharging member (32) for the discharge <strong>of</strong> milk from the teatcup,<br />
and a milk channel arranged to extend between the lower opening <strong>of</strong> the<br />
inner space <strong>of</strong> the teatcup liner and the milk-discharging member when<br />
the teatcup part is mounted to the connection part. The connection part<br />
includes a pulse supplying member for the supply <strong>of</strong> a pulsating pres-<br />
sure to the pulsation chamber, and a pulse channel arranged to extend<br />
between the pulsation chamber and the pulse-supplying member when<br />
the teatcup part is mounted to the connection part. The pulsation chamber<br />
is accessible via an aperture through the shell, and the pulse channel<br />
connects to the aperture when the teatcup part is mounted to the<br />
connection part. A sealing element is provided at the connection between<br />
the aperture and the pulse channel.<br />
(21) 553810 (22) 6 Sep 2005<br />
(54) A nozzle which pivots between two positions for dosing <strong>of</strong> a material<br />
from a container<br />
(86) PCT/DK2005/000567 (87) WO2006/026990<br />
(51) IPC2011.01:B05C17/005; B65D25/46<br />
(71) CLAUS LEONHARDT JENSEN; FINN HOLME HJORT<br />
(72) Hjort, Finn Holme;<br />
(31) 04 01342 (32) 6 Sep 2004 (33) DK<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) A nozzle (1) for use in connection with the dosing <strong>of</strong> a material from a<br />
container is disclosed. The nozzle includes a first nozzle base part (2), a<br />
nozzle tip part (3), and a link (4) connecting the nozzle parts. The link has<br />
a first pivotal state and a second locked state when the link is under<br />
pressure by the material flow. The link includes a first surface and a<br />
second surface. The surfaces are pivotally connected to each other and<br />
the surfaces are angled in relation to the longitudinal centre axis <strong>of</strong> the<br />
nozzle. In a first position <strong>of</strong> the first nozzle base part and nozzle tip part,<br />
the first nozzle base part and nozzle tip part form a conical internal flow<br />
channel, where no part <strong>of</strong> the link protrudes into the conical internal flow<br />
channel.<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 61 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(21) 554057 (22) 23 Sep 2005<br />
(54) Compression garment with seam corresponding to muscle ridge<br />
(86) PCT/AU2005/001450 (87) WO2006/032096<br />
(51) IPC2011.01:A41D1/08; A41D13/00,05; A41D27/00,24<br />
(71) Skins Capital Pty Limited<br />
(72) Duffy, Bradley Thomas; Duffy, Susan Kathleen;<br />
(31) 04 905456 (32) 23 Sep 2004 (33) AU<br />
(74) JAMES & WELLS, Level 12, KPMG Centre, 85 Alexandra Street,<br />
Hamilton, New Zealand<br />
(57) A compression garment (50) for clothing a body part, such as a lower<br />
torso and the legs. The body part includes a muscle ridge, such as a<br />
lateral edge <strong>of</strong> the gluteus maximus (49). Compression garment has first<br />
and second panels <strong>of</strong> stretchable material joined by a seam (32). At least<br />
part <strong>of</strong> the seam is adapted to correspond to at least part <strong>of</strong> the muscle<br />
ridge so that in use a muscle group is substantially supported by the first<br />
or second panel. The garment is adapted to effect a compression <strong>of</strong><br />
between 5mmHg and 40mmHg.<br />
Divisional filed as 581314<br />
(21) 554517 (22) 19 Oct 2005<br />
(54) Flavonoid composition for treating oral diseases<br />
(86) PCT/US2005/037936 (87) WO2006/045056<br />
(51) IPC2011.01:A61K31/35; A61K9/68,00; A61K47/00; A61K9/14; A61K8/<br />
00,97; A61K36/539,48,74<br />
(71) Unigen Pharmaceuticals, Inc.<br />
(72) Jia, Qi; Zhao, Yuan;<br />
(31) 04 620163 (32) 19 Oct 2004 (33) US<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) Disclosed is a pharmaceutical composition comprising a mixture <strong>of</strong> at<br />
least one Free-B-Ring flavonoid and at least one flavan; wherein said<br />
Free-B-ring flavonoid is isolated from a plant or plants in the Scutellaria<br />
genus <strong>of</strong> plants and said flavan is isolated from a plant or plants in the<br />
Acacia or Uncaria genus <strong>of</strong> plants. The composition is useful for the<br />
preparation <strong>of</strong> a medicament for preventing and treating diseases and<br />
conditions <strong>of</strong> the mouth, gums and teeth, selected from the group consisting<br />
<strong>of</strong>: gingivitis; periodontitis; pulpitis; periodontal conditions caused<br />
by the physical implantation <strong>of</strong> oral dentures, trauma, injuries, bruxism,<br />
neoplastic and other degenerative processes; material alba; pellicles;<br />
dental plagues; calculus; and stains; or for maintaining optimum saliva<br />
production and pH; minimizing bacterial growth; reducing the formation<br />
<strong>of</strong> pellicles and plague; inhibiting tooth decalcification and tooth caries<br />
(decay); promoting remineralization; whitening teeth; maintaining healthy<br />
oral hygiene; and reducing oral malodour (halitosis).<br />
Divisional filed as 590647<br />
(21) 554561 (22) 19 Oct 2005<br />
(54) Permeate Tube<br />
(86) PCT/SE2005/001554 (87) WO06/043884<br />
(51) IPC2011.01:B01D63/10<br />
(71) ALFA LAVAL CORPORATE AB<br />
(72) Larsen, Knud Verner;<br />
(31) 04 0402542 (32) 20 Oct 2004 (33) SE<br />
(31) 04 0403169 (32) 22 Dec 2004 (33) SE<br />
(74) HENRY HUGHES, 119-125 Willis Street, Wellington, New Zealand<br />
(57) A permeate tube for spiral wound membrane which comprises at least<br />
one tubular unit (1) is disclosed. Spaced substantially along the unit's<br />
length are a plurality <strong>of</strong> permeate transfer means (2) enabling permeate<br />
transfer from an external surface region <strong>of</strong> the unit to an internal passageway<br />
<strong>of</strong> the unit. One or more grooves (3) in the external surface<br />
form flow channels connect the permeate transfer means. At least a part<br />
<strong>of</strong> the internal passageway <strong>of</strong> each tubular unit has a polygonal crosssection.<br />
(21) 554779 (22) 30 Jan 2006<br />
(54) Injectable preparations <strong>of</strong> dicl<strong>of</strong>enac ((2,6-dichloranilino)phenylacetic<br />
acid) and its pharmaceutically acceptable salts<br />
(86) PCT/IN2006/000033 (87) WO2006/095363<br />
(51) IPC2011.01:A61K31/196; A61K9/08; C07C229/40<br />
(71) Troikaa Pharmaceuticals Ltd.<br />
(72) Patel, Ketan Rajnibhai; Patel, Milan Rajnibhai;<br />
(31) 96/MUM/2005 (32) 1 Feb 2005 (33) IN<br />
(74) F B RICE & CO, Level 23, 44 Market Street, Sydney, New South<br />
Wales 2000, Australia<br />
(57) Disclosed is an injectable preparation containing about 75 mg/ml to<br />
about 100 mg/ml <strong>of</strong> dicl<strong>of</strong>enac sodium or therapeutically equivalent<br />
amounts <strong>of</strong> alternative pharmaceutically acceptable water-soluble salts<br />
<strong>of</strong> dicl<strong>of</strong>enac, said preparations having a viscosity <strong>of</strong> about 1.5 to about<br />
4.7 CPS and a pH <strong>of</strong> about 6-10; said preparations further comprising<br />
either: a) a co-solvent/solubiliser selected from a monohydric alcohol<br />
(such as benzyl alcohol or ethyl alcohol) present in the composition at<br />
about 4% to about 25% v/v, or tetrahydr<strong>of</strong>urfuryl alcohol polyethylene<br />
glycol ether (glyc<strong>of</strong>urol) present in the composition at about 18 to about<br />
35% v/v; in combination with water and optional pharmaceutically acceptable<br />
excipient(s); or b) a solvent system comprising combinations <strong>of</strong><br />
at least two or more cosolvents/solubilisers selected from differing classes,<br />
wherein the co-solvents/solubilisers are selected from monohydric<br />
alcohol(s) present in the composition up to about 15% v/v; polyhydric<br />
alcohol(s) (such as propylene glycol or a polyethylene glycol) present in<br />
the composition up to about 15% v/v; and tetrahydr<strong>of</strong>urfuryl alcohol<br />
polyethylene glycol ether (glyc<strong>of</strong>urol) present in the composition up to<br />
about 25% v/v; in combination with water and optional pharmaceutically<br />
acceptable excipient(s).<br />
(21) 555075 (22) 28 Nov 2005<br />
(54) Compositions for combating beta-lactamase-mediated antibiotic resistance<br />
using ceftriaxone, sulbactam and EDTA<br />
(86) PCT/IN2005/000382 (87) WO2006/059344<br />
(51) IPC2011.01:A61K31/546,46; A61K9/00; A61P31/04<br />
(71) VENUS REMEDIES LIMITED<br />
(72) Chaudhary, Manu;<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 62 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(31) 04DEL 2411 (32) 2 Dec 2004 (33) IN<br />
(74) A.P.T. PATENT AND TRADE MARK ATTORNEYS, 383 Goodwood<br />
Road, Westbourne Park, SA 5041, Australia<br />
(57) Disclosed is a pharmaceutical composition for combating betalactamase<br />
mediated antibiotic resistance, said pharmaceutical composition<br />
comprising a beta-lactam antibiotic, wherein said beta-lactam antibiotic<br />
is ceftriaxone or a pharmaceutically acceptable salt there<strong>of</strong>, which<br />
is ceftriaxone sodium;a beta-lactamase inhibitor, wherein said betalactamase<br />
inhibitor is sulbactam or a pharmaceutically acceptable salt<br />
there<strong>of</strong>, which is sulbactam sodium; wherein said beta-lactam antibiotic<br />
and said beta-lactamase inhibitors are present in a weight ratios <strong>of</strong> 1:4 to<br />
4:1 along with EDTA or a pharmaceutically acceptable salt there<strong>of</strong>.<br />
(21) 555287 (22) 28 Nov 2005<br />
(54) Solid formulations <strong>of</strong> liquid biologically active agents such as prop<strong>of</strong>ol<br />
(86) PCT/CA2005/001790 (87) WO2006/056064<br />
(51) IPC2011.01:A61K31/47,05,08; A61K47/30; A61K9/10,14<br />
(71) LABOPHARM EUROPE LIMITED; LABOPHARM (BARBADOS) LIM-<br />
ITED; LABOPHARM INC.<br />
(72) Ravenelle, Francois; Gori, Sandra; Lessard, David; Luo, Laibin; Le<br />
Garrec, Dorothee; Smith, Damon;<br />
(31) 04 631755 (32) 29 Nov 2004 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed is a solid product suitable for reconstitution to an essentially<br />
clear, stable aqueous solution, comprising an intimate mixture <strong>of</strong><br />
at least one amphiphilic copolymer which includes a hydrophilic part that<br />
comprises at least one member selected from the group consisting <strong>of</strong><br />
poly(N-vinylpyrrolidone), poly(N-2-hydroxypropylmethacrylamide), poly(2ethyl-2oxazoline),<br />
poly(glycidol), poly(2-hydroxyethylmethacrylate),<br />
poly(vinylalcohol), polymethacrylic acid derivatives, poly(vinylpyridinium),<br />
poly((ammoniumalkyl)methacrylate), poly((aminoalkyl)methacrylate) and<br />
combinations and derivatives there<strong>of</strong>, and at least one liquid biologically<br />
active agent such as prop<strong>of</strong>ol loaded within said amphiphilic copolymer,<br />
in such a manner that said liquid biologically active agent is intimately<br />
associated with said amphiphilic copolymer in a substantially solid product;<br />
The aqueous solution which is produced by reconstituting the solid<br />
contains the biologically active agent as stable nanodispersions or micelles<br />
and is substantially free <strong>of</strong> organic solvent. Also disclosed is an<br />
apparatus and a process for preparing the solid product comprising forming<br />
an aqueous solution <strong>of</strong> at least one linear, branched or star-shaped<br />
amphiphilic copolymer, under conditions to achieve micelle or<br />
nanodispersion formation; adding the liquid biologically active agent to<br />
the solution to form a second mixture; and treating said second mixture<br />
under conditions effective to remove water, while forming a substantially<br />
solid product.<br />
(21) 555399 (22) 29 Nov 2005<br />
(54) Residential fire sprinkler with heat responsive trigger and deflective<br />
tines with slots<br />
(86) PCT/US2005/042816 (87) WO2006/060287<br />
(51) IPC2011.01:A62C37/08,14; B05B1/26<br />
(71) TYCO FIRE PRODUCTS LP<br />
(72) Rogers, Kenneth W.; Fesseden, Mark E.; Silva, Jr., Manuel R.;<br />
(31) 04 000128 (32) 1 Dec 2004 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) A residential fire sprinkler comprises a body defining a passageway<br />
26 between an inlet 26A and an outlet 26B along a longitudinal axis with<br />
the outlet closer to an area to be protected than the inlet, the passageway<br />
having a rated K-factor <strong>of</strong> at least 6, the body including a portion<br />
having ¾ inch or greater NPT threads formed thereon, a closure positioned<br />
proximate the outlet opening so as to occlude the passageway<br />
26, a heat responsive trigger 36 that retains the closure to occlude the<br />
passageway 26, at least one frame arm 14 being coupled to the body<br />
and a deflector coupled to the at least one frame arm 14 and spaced<br />
from the outlet opening so that when the trigger is actuated, the deflector<br />
provides adequate fluid distribution for the protection <strong>of</strong> a dwelling unit,<br />
the deflector including a first surface that faces the outlet and a second<br />
surface spaced apart from the first surface, a plurality <strong>of</strong> tines that extends<br />
away from the longitudinal axis, the plurality <strong>of</strong> tines being disposed<br />
generally about the longitudinal axis and two slots formed through<br />
the first and second surfaces, each slot including two generally parallel<br />
walls between a first end and a second end to define an opening extending<br />
along a first axis generally perpendicular to a plane defined by the<br />
longitudinal axis and the at least one frame arm, the two walls <strong>of</strong> the slot<br />
converging towards each other at the first end and the second end to<br />
define a close-ended slot 40 having a generally polygonal perimeter.<br />
(21) 555406 (22) 2 Dec 2005<br />
(54) Cytotoxic agents comprising new taxanes<br />
(86) PCT/EP2005/014177 (87) WO2006/061258<br />
(51) IPC2011.01:C07D493/06; A61K39/395; A61P35/00; C07K16/30<br />
(71) AVENTIS PHARMA S.A.<br />
(72) Miller, Michael L.; Chari, Ravi V. J.; Baloglu, Erkan; Commercon, Alain;<br />
(31) 04 04292898 (32) 7 Dec 2004 (33) EP<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 63 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(57) Disclosed are Taxane compounds having the following formula (I)<br />
wherein R1 is a linker group comprising a disulfide group, or is an aryl or<br />
heterocyclic radical, alkyl alkenyl or alkynyl, cycloalkyl or cycloalkenyl, -<br />
OR2 or a carbamate formed from any <strong>of</strong> said, alkenyl or alkynyl, cycloalkyl<br />
or cycloalkenyl, or aryl or heterocyclyl; R2 is an alkyl, alkenyl or alkynyl,<br />
cycloalkyl or cycloalkenyl, aryl or heterocyclic; R3 is a linker group comprising<br />
a disulfide group, or is an aryl or heterocyclic, alkyl, alkenyl or<br />
alkynyl, cycloalkyl or cycloalkenyl; R4 is a linker group comprising a<br />
disulfide group, H, or is a hydroxy, an alkoxy, an alkenyloxy, an alkanoyloxy,<br />
aroyloxy, alkenoyloxy, alkynoyloxy, cycloalkanoyloxy, alkoxyacetyl,<br />
alkylthioacetyl, alkyloxycarbonyloxy, cycloalkyloxy, cycloalkenyloxy,<br />
carbamoyloxy, alkylcarbamoyloxy, or dialkylcarbamoyloxy, a heterocyclic<br />
or aryl ether, ester or carbamate, or alkyl or alkenyl ester or ether or a<br />
carbamate <strong>of</strong> the formula -OCOX, wherein X is a nitrogen-containing<br />
heterocycle or a carbamate <strong>of</strong> the formula –OCONR9R10, wherein R9<br />
and R10 are the same or different and are H, alkyl or aryl; R8 or R7 is H;<br />
Ra is H; R7 or R8 and R form a bond (cyclic ether); Ra = aryl or heterocyclic<br />
radical; and wherein R, or R3 or R4 represents said linking group. Also<br />
disclosed is a cytotoxic agent comprising said taxane and a cell binding<br />
agent e.g. an antibody.<br />
(21) 555470 (22) 17 Nov 2005<br />
(54) Rasagiline orally disintegrating compositions<br />
(86) PCT/US2005/041882 (87) WO2006/057912<br />
(51) IPC2011.01:A61K31/135<br />
(71) TEVA PHARMACEUTICAL INDUSTRIES, LTD.<br />
(72) Patashnik, Shulamit; Licht, Daniella; Gilbert, Adrian;<br />
(31) 04 630918 (32) 24 Nov 2004 (33) US<br />
(31) 04 997785 (32) 24 Nov 2004 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed is a solid pharmaceutical composition comprising rasagiline<br />
or a pharmaceutical acceptable salt <strong>of</strong> rasagiline, and particles having a<br />
non-filamentous microstructure <strong>of</strong> at least two sugar alcohols.<br />
(21) 555634 (22) 30 Nov 2005<br />
(54) Adjustable bracket for securing vessel to surface with flexible straps<br />
and slidable portions in receiving track<br />
(86) PCT/AU2005/001797 (87) WO2006/058366<br />
(51) IPC2011.01:F16M13/02; A62C13/78; A62B25/00; F17C13/08<br />
(71) Wilro<strong>of</strong> Products (WA) Pty Ltd<br />
(72) Larmont, James;<br />
(31) 04 906814 (32) 30 Nov 2004 (33) AU<br />
(74) P L BERRY & ASSOCIATES, AEQ Building, 61 Cambridge Terrace,<br />
Christchurch 8013, New Zealand<br />
(57) An adjustable bracket (10) for securing a vessel to a surface includes<br />
slidable portions (12) and receiving track (14) mounted on the surface.<br />
Each slidable portion (12) includes a track engaging portion (16) positioned<br />
within track (14), an outwardly extending portion (18) and a flexible<br />
member (34) attached to engaging portion (32). In use, slidable portions<br />
(12) are positioned adjacent opposing sides <strong>of</strong> the vessel and flexible<br />
members (34) are fastened around the vessel such that tension in<br />
flexible members (34) causes slidable portions (12) to be held in place<br />
upon track (14) by friction. The vessel may be a portable fire extinguisher<br />
or oxygen tank and the surface might be a wall.<br />
(21) 555721 (22) 22 Dec 2005<br />
(54) Fused pyrazole derivatives and uses there<strong>of</strong> in methods <strong>of</strong> treatment<br />
<strong>of</strong> metabolic-related disorders<br />
(86) PCT/US2005/046599 (87) WO06/069242<br />
(51) IPC2011.01:C07D231/54; A61K31/4155,416; A61P9/10; C07D403/<br />
04<br />
(71) Arena Pharmaceuticals, Inc.<br />
(72) Boatman, Douglas P; Schrader, Thomas O; Semple, Graeme; Skinner,<br />
Philip J; Jung, Jae-Kyu;<br />
(31) 04 638668 (32) 23 Dec 2004 (33) US<br />
(31) 05 676521 (32) 29 Apr 2005 (33) US<br />
(74) F B RICE & CO, Level 23, 44 Market Street, Sydney, New South<br />
Wales 2000, Australia<br />
(57) Disclosed herein are fused pyrazole derivatives <strong>of</strong> Formula (Ia), and<br />
pharmaceutically acceptable salts there<strong>of</strong> wherein substituents are as<br />
defined within the specification. Such compounds exhibit useful pharmacological<br />
properties, for example, as agonists for the RUP25 receptor.<br />
Also disclosed are pharmaceutical compositions containing said compounds<br />
and methods <strong>of</strong> using the compounds and compositions <strong>of</strong> the<br />
invention in the treatment <strong>of</strong> metabolic-related disorders, including<br />
dyslipidemia, atherosclerosis, coronary heart disease, insulin resistance,<br />
type 2 diabetes, Syndrome-X and the like. The use <strong>of</strong> the compounds <strong>of</strong><br />
Formula (Ia) in combination with other active agents such as those belonging<br />
to the class <strong>of</strong> á-glucosidase inhibitors, aldose reductase inhibitors,<br />
biguanides, HMG-CoA reductase inhibitors, squalene synthesis inhibitors,<br />
fibrates, LDL catabolism enhancers, angiotensin converting enzyme<br />
(ACE) inhibitors, insulin secretion enhancers, DP receptor antagonists,<br />
and the like are further disclosed.<br />
(21) 555813 (22) 2 Dec 2005<br />
(54) Wall construction method using tilt-up wall panel with lengthwise extending<br />
rib supported on a structure with rebate<br />
(86) PCT/AU2005/001835 (87) WO2006/058390<br />
(51) IPC2011.01:E04B2/08,82,94<br />
(71) BLUESCOPE STEEL LIMITED<br />
(72) Kralic, John; Contouris, Samuel;<br />
(31) 04 906945 (32) 3 Dec 2004 (33) AU<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) A method <strong>of</strong> constructing a wall on a wall support structure having<br />
rebate is disclosed. A tilt-up wall panel (3) that is used in the method<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 64 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
includes a composite slab having a pr<strong>of</strong>iled decking sheet (5) with at<br />
least one lengthwise extending rib (9). Concrete is casted on the pr<strong>of</strong>iled<br />
decking sheet (5). Firstly, a tilt-up wall panel (3) is positioned so that that<br />
the panel (3) rests on a horizontal surface <strong>of</strong> the wall support structure<br />
and extends vertically upwardly with the rib(s) (9) forming an internal<br />
face <strong>of</strong> the wall. Then, the wall panel (3) and wall support structures are<br />
connected together with at least one connecting means via the engagement<br />
<strong>of</strong> the connection means with a rib(s) (9) <strong>of</strong> the wall panel (3).<br />
Divisional filed as 590093<br />
(21) 556050 (22) 6 Dec 2005<br />
(54) Sleeved container package with V shaped opening feature and a<br />
plastic carrier with acontainer holding portion <strong>of</strong> interconnected stretchable<br />
loops<br />
(86) PCT/IB2005/054087 (87) WO2006/067651<br />
(51) IPC2011.01:B65D71/50,12,28,34,06<br />
(71) Illinois Tool Works Inc.<br />
(72) Marco, Leslie S;<br />
(31) 04 021263 (32) 23 Dec 2004 (33) US<br />
(74) PHILLIPS ORMONDE FITZPATRICK, 367 Collins Street, Melbourne,<br />
Victoria 3000, Australia<br />
(57) A package 10 for containers 16 such as beverage bottles and cans<br />
includes a plastic carrier 20 with an array 50 <strong>of</strong> interconnected, stretchable<br />
loops, with one loop being provided for surrounding each container<br />
16. A sleeve 14 surrounds the group 18 <strong>of</strong> containers 16 held by the<br />
carrier 20. The sleeve 14 includes two parting lines 50, 52 with edges<br />
positioned to open the edges <strong>of</strong> the sleeve, and a tear-initiating breach<br />
60 placed substantially between two <strong>of</strong> the carrier loops and at the intersection<br />
<strong>of</strong> the parting lines 50, 52. The tear-initiating breach 60 comprises<br />
perforations in the sleeve arranged in a ‘V’ configuration. The arrangement<br />
gives the container package an easy and convenient opening<br />
feature.<br />
(21) 556150 (22) 30 Dec 2005<br />
(54) 18-methyl-19-NOR-17-pregn-4-en-21,17 carbolactones and pharmaceutical<br />
preparations comprising the same<br />
(86) PCT/EP2005/014205 (87) WO2006/072467<br />
(51) IPC2011.01:C07J53/00; A61K31/585; A61P5/34<br />
(71) BAYER SCHERING PHARMA AKTIENGESELLSCHAFT<br />
(72) Borden, Steffen; Bohlmann, Rolf; Bittler, Dieter; Kuenzer, Hermann;<br />
Esperling, Peter; Muhn, Hans-Peter; Fritzemeier, Karl-Heinrich; Fuhrmann,<br />
Ulrike; Prelle, Katja;<br />
(31) 04 0463864 (32) 30 Dec 2004 (33) DE<br />
(74) HENRY HUGHES, 119-125 Willis Street, Wellington, New Zealand<br />
(57) Disclosed herein are 18-methyl-19-nor-17-pregn-4-en-21,17carbolactones<br />
<strong>of</strong> general formula (I), wherein the substituents are as<br />
defined in the specification. Said compounds have gestagenic and<br />
antimineralocorticoid activity and are suitable for the production <strong>of</strong> pharmaceutical<br />
preparations, for example, for oral contraception and the treatment<br />
<strong>of</strong> pre-, peri- and post-menopausal pain.<br />
(21) 556210 (22) 19 Dec 2005<br />
(54) Tool having an integral wireless system for remotely ordering replacement<br />
consumables<br />
(86) PCT/IB2005/054322 (87) WO2006/077473<br />
(51) IPC2011.01:B25B33/00; G06Q10/00<br />
(71) Illinois Tool Works Inc.<br />
(72) Panasik, Cheryl L;<br />
(31) 05 040978 (32) 21 Jan 2005 (33) US<br />
(74) DAVIES COLLISON CAVE - MELBOURNE, 1 Nicholson Street, Melbourne,<br />
Victoria, Australia<br />
(57) A wireless system for a host power tool 10 having an integral system<br />
for ordering replacement consumables from an inventory order interface<br />
comprises a processing unit 18, a location provider 14 and a remote<br />
connector 16. The location provider 14 is configured to selectively provide<br />
the location <strong>of</strong> the host tool 10 to the processing unit 18, while the<br />
remote connector 16 is configured to establish a remote connection between<br />
the processing unit 18 and the inventory order interface <strong>of</strong> the<br />
supplier <strong>of</strong> the replacement consumables. A customer identification card<br />
having order information is selectively connected to the host tool 10.<br />
When the card is connected, the information is read by and transmitted<br />
from the host tool 10 to the inventory order interface through the remote<br />
connector 16. The processing unit 18 is configured to interface location<br />
information from the location provider 14 payment information and order<br />
information from the customer identification card, through the remote<br />
connector 16, to place an order for the replacement consumables <strong>of</strong> the<br />
host tool 10 at the inventory order interface. The system simplifies the<br />
ordering <strong>of</strong> replacement consumables like fasteners for the host power<br />
tool.<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 65 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(21) 556245 (22) 5 Jan 2006<br />
(54) Composition for treating wood, method for treatment <strong>of</strong> wood and<br />
wood product<br />
(86) PCT/FI2006/050012 (87) WO2006/072672<br />
(51) IPC2011.01:B27K3/50; A01N37/06,10,02<br />
(71) BIO-TEHO OY<br />
(72) Aitta, Eero; Seppi, Pekka; Kukkonen, Jari; Nissinen, Timo;<br />
(31) 05 050023 (32) 10 Jan 2005 (33) FI<br />
(74) P L BERRY & ASSOCIATES, AEQ Building, 61 Cambridge Terrace,<br />
Christchurch 8013, New Zealand<br />
(57) Disclosed is a method for the treatment <strong>of</strong> wood, in which a treatment<br />
composition and wood are brought into a contact with each other and the<br />
treatment composition contains formate salt characterized in that the<br />
treatment composition used is a composition which contains 1) the formate<br />
salt together with 2) sorbate salt and/or benzoate salt dissolved in<br />
an aqueous liquid carrier. Also disclosed is a wood material treated by<br />
said method.<br />
(21) 556312 (22) 25 Jan 2006<br />
(54) Container with two packs joined by straps in a Jacob’s Ladder arrangement<br />
(86) PCT/GB2006/000245 (87) WO2006/079799<br />
(51) IPC2011.01:B65D5/00; B65D21/02; B65D5/42; B65D71/02; B65D85/<br />
10<br />
(71) British American Tobacco (Investments) Ltd<br />
(72) Bray, Andrew Jonathan; Tearle, Alan Douglas;<br />
(31) 05 0501733 (32) 27 Jan 2005 (33) GB<br />
(74) Shelston IP, Level 21, 60 Margaret Street, Sydney, NSW 2000, Australia<br />
(57) A package comprises first and second packs Pl, P2 each capable <strong>of</strong><br />
containing items. Each pack has a first face Fl, Fl' bound by a first edge<br />
El, El' and a second edge E2, E2'. The first and second packs Pl, P2 are<br />
connected by first and second straps Sl, S2. In a first position <strong>of</strong> the<br />
packs the first faces Fl, Fl' <strong>of</strong> each pack face each other with the first<br />
edges El, El' <strong>of</strong> the first and second packs adjacent each other and the<br />
second edges El, E2' <strong>of</strong> the first and second packs adjacent each other.<br />
The first and second straps Sl, S2 extend across the first faces Fl, Fl' <strong>of</strong><br />
the packs, the first strap Sl is hinged relative to the first pack at the first<br />
edge El <strong>of</strong> the first pack and hinged relative to the second pack at the<br />
second edge E2' <strong>of</strong> the second pack, and the second strap S2 is hinged<br />
relative to the second pack P2 at the first edge El' <strong>of</strong> the second pack<br />
and hinged relative to the first pack at the second edge <strong>of</strong> the first pack.<br />
When connected together by the straps Sl, S2, the first and second packs<br />
Pl, P2 are moveable, one relative to the other between at least the first<br />
position, a second position in which the second pack P2 is rotated relative<br />
to the first pack Pl about the first edge El and a third position in which<br />
the second pack P2 is rotated relative to the first pack Pl about the second<br />
edge E2'.<br />
(21) 556318 (22) 4 Jan 2006<br />
(54) N-(heteroaryl)-1H-indole-2-carboxamide derivatives and their use as<br />
vanilloid TRPV1 receptor ligands<br />
(86) PCT/FR2006/000008 (87) WO2006/072736<br />
(51) IPC2011.01:C07D209/42; A61K31/33; A61P29/00; C07D401/12;<br />
C07D403/12; C07D405/12; C07D413/12; C07D417/12<br />
(71) san<strong>of</strong>i-aventis<br />
(72) Dubois, Laurent; Evanno, Yannick; Malanda, Andre;<br />
(31) 05 0550068 (32) 7 Jan 2005 (33) FR<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed are N-(heteroaryl)-1H-indole-2-carboxamide-based compounds<br />
<strong>of</strong> formula (I) wherein W is a fused bicyclic group and the remaining<br />
substituents are as defined in the specification, a process for<br />
preparing compounds <strong>of</strong> formula (I) and their agonist or antagonist effects<br />
on the TRPV1 receptor. Also disclosed is their use in treating diseases<br />
such as pain and inflammation, urological disorders, gynaecological<br />
disorders, gastrointestinal disorders, respiratory disorders, psoriasis,<br />
pruritus, dermal, ocular or mucous irritation, herpes and zona.<br />
(21) 556478 (22) 31 Jan 2006<br />
(54) DR5 antibodies and uses there<strong>of</strong><br />
(86) PCT/US2006/003577 (87) WO2006/083971<br />
(51) IPC2011.01:C07K16/28<br />
(71) GENENTECH, INC.<br />
(72) Adams, Camellia W;<br />
(31) 05 649550 (32) 2 Feb 2005 (33) US<br />
(31) 06 344564 (32) 30 Jan 2006 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Provided is an anti-DRS antibody comprising mutations in the heavy<br />
and light chain <strong>of</strong> full-length antibody 16E2, or a fragment there<strong>of</strong>, wherein:<br />
said antibody or antibody fragment has a greater affinity for DRS than<br />
full-length antibody 16E2 and is capable <strong>of</strong> activating or stimulating<br />
apoptosis in cancer cells; and the mutations comprise: (i) a set <strong>of</strong> heavy<br />
chain mutations selected from the group consisting <strong>of</strong> (i) NS3Q, L102Y;<br />
(ii) M34L, N53Q, L102Y; (iii) N53Y, L102Y;(iv) M34L, N53Y, L102Y; (v)<br />
G33A, N53Q, L102Y; (vi) M34L, N53Y, L102Y; (vii) G33A, N53Q, L102Y;<br />
(viii) G33A, N53Y, L102Y; (ix) T28A, N53Q, L102Y; and (x) T28A, NS3Y,<br />
L102Y; and (ii) a set <strong>of</strong> light chain mutations selected from the group<br />
consisting <strong>of</strong> (i) Q24S, G50K, K51D, H95bY; (ii) Q24S, K51A, D92S,<br />
S93Y; and (iii) Q24S, K51A, R91A in the amino acid sequence. The antibodies<br />
can be used to treat cancer.<br />
(21) 556499 (22) 3 Feb 2006<br />
(54) Methods and materials with trans-clomiphene for the treatment <strong>of</strong><br />
male infertility<br />
(86) PCT/US2006/003882 (87) WO2006/084153<br />
(51) IPC2011.01:A61K31/137<br />
(71) REPROS THERAPEUTICS INC.<br />
(72) Podolski, Joseph;<br />
(31) 05 650018 (32) 4 Feb 2005 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed is the use <strong>of</strong> a composition comprising an effective amount<br />
<strong>of</strong> trans-clomiphene or a pharmaceutically acceptable sale tor solvate<br />
there<strong>of</strong> and optionally one or more pharmaceutically acceptable diluents,<br />
adjuvants, carriers or excipients in the manufacture <strong>of</strong> a medicament for<br />
treating infertility in a male with secondary hypogonadism wherein the<br />
composition is characterized by the following: a)the ratio <strong>of</strong> transchlomiphene<br />
to cis-clomiphene is greater than 71/29; or b) the composition<br />
comprises 0% to 29% w/w <strong>of</strong> cis-clomiphene and 100% to 71% transclomiphene.<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 66 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(21) 556546 (22) 6 Jan 2006<br />
(54) Compounds for inflammation and immune-related uses<br />
(86) PCT/US2006/000296 (87) WO2006/083477<br />
(51) IPC2011.01:A61K31/537,455,433,415; C07D213/02; A61K31/44<br />
(71) SYNTA PHARMACEUTICALS CORP.<br />
(72) Sun, Lijun; Chen, Shoujun; Xia, Zhi Qiang; Jiang, Jun; Xie, Yu; Zhang,<br />
Junyi;<br />
(31) 05 642179 (32) 7 Jan 2005 (33) US<br />
(31) 05 707845 (32) 12 Aug 2005 (33) US<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) Disclosed is a compound <strong>of</strong> formula (I), wherein L is a linker selected<br />
from the group <strong>of</strong> a covalent bond, -NRCH2-, -CH2NR-, -C(O)-, -NR-<br />
C(O)-, -C(O)-NR-, OC(O)-, C(O)O-, C(S)-, -NR-C(S)- or –C(S)-NR-, and<br />
the other substituents are disclosed within the specification, or a<br />
pharmaceutically acceptable salt there<strong>of</strong>. Also disclosed is a method <strong>of</strong><br />
inhibiting immune cell activation, inhibiting cytokine production or modulating<br />
an ion channel in a cell in vitro, comprising administering to the cell<br />
the said compound. Use <strong>of</strong> the said compound for the manufacture <strong>of</strong> a<br />
medicament for inhibiting immune cell activation, inhibiting cytokine production<br />
or modulating an ion channel in a cell is also disclosed.<br />
(21) 556620 (22) 15 Feb 2006<br />
(54) Mechanically operated nail advancement systems for nail arrays disposed<br />
within nailing tool magazines<br />
(86) PCT/US2006/005194 (87) WO2006/091433<br />
(51) IPC2011.01:B25C1/00; B25F5/00; B25C1/18<br />
(71) Illinois Tool Works Inc.<br />
(72) Porth, Chris H; Moeller, Larry M; Walthall, Barry C; Henry, Clayton D;<br />
(31) 05 060864 (32) 18 Feb 2005 (33) US<br />
(74) DAVIES COLLISON CAVE - MELBOURNE, 1 Nicholson Street, Melbourne,<br />
Victoria, Australia<br />
(57) A fastener advancement system for example advancing the nail in<br />
the magazine <strong>of</strong> a nail gun using electromechanically operated mechanism<br />
is disclosed. The system comprises a driving means consisting <strong>of</strong><br />
multi-lever and linkage (136) that are operatively connected to the blade<br />
member (126) <strong>of</strong> the fastener driving tool for advancing a leading fastener<br />
<strong>of</strong> a collated strip <strong>of</strong> fasteners into the driver blade channel <strong>of</strong> the<br />
fastener-driving tool. The system is characterised by the means for separating<br />
the leading fastener <strong>of</strong> the collated strip <strong>of</strong> fasteners that is movable<br />
in response to the rearward movement <strong>of</strong> the driving means. The<br />
system uses push type; pull type and rotary solenoid actuating members<br />
for moving the fastener-advancement feed pawl or claw member. Since<br />
the system is electromechanically operated it eliminates the need <strong>of</strong> any<br />
exhaust gases that would otherwise be required in the combustion powered<br />
fastener advancement system.<br />
(21) 556623 (22) 8 Feb 2006<br />
(54) A beehive lid which avoids propolis around the lids opening<br />
(86) PCT/GR2006/000006 (87) WO2006/085124<br />
(51) IPC2011.01:A01K47/00; A01K53/00<br />
(71) Ioannis Katsampis<br />
(72) Katsampis, Ioannis;<br />
(31) 05 0100057 (32) 9 Feb 2005 (33) GR<br />
(74) Acacia Law, 16 Brasenose Place, Tawa, Wellington, 5028, New Zealand<br />
(57) A beehive lid is disclosed. The lid includes a top cover that opens<br />
using a connecting mechanism (1), there are containers (8) under the<br />
top cover (10) for placement <strong>of</strong> liquid, and a surface (24, 25) attached to<br />
the sidewalls (2) <strong>of</strong> the lid. The surface has an opening (9) that is covered<br />
by a removable cover (48). One side (26) <strong>of</strong> the surface <strong>of</strong> the lid is<br />
inclined coming down into the containers leaving a gap between its end<br />
and the bottom (30) <strong>of</strong> the container (8). The liquids are transferred through<br />
the gap inside the body <strong>of</strong> the lid (99) to a space (7). The space is defined<br />
by walls having stripes to help the bees to climb up easily, and<br />
prevent immediate contact with the top (10) <strong>of</strong> the lid so they do not glue<br />
it with "propolis". This gives immediate access to the liquids in the containers<br />
(8) without having any contact with the bees and gives the ability<br />
to open the removable cover (48) to place anything inside or take anything<br />
out. On the top <strong>of</strong> the lid (10) there are shutters (11) that open and<br />
are adjustable to help the bees overcome any extreme weather conditions.<br />
When the shutters are closed, they cover the air intake holes. All<br />
the above are done without taking the lid (99) <strong>of</strong>f and without smoking<br />
the bees, this avoids transferring the toxic substances <strong>of</strong> the smoke to<br />
the bees' products.<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 67 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(21) 556716 (22) 8 Feb 2005<br />
(54) Site-specific serine recombinases from Mycobacterium tuberculosis<br />
phage phiRv1 and M. smegmatis phage Bxb1and methods <strong>of</strong> their use<br />
(86) PCT/US2005/003851 (87) WO2006/083253<br />
(51) IPC2011.01:C12N15/85; C07H21/04<br />
(71) Intrexon Corporation<br />
(72) Padidam, Malla;<br />
(31) 05 49552 (32) 2 Feb 2005 (33) US<br />
(74) Freehills <strong>Patent</strong> & Trade Mark Attorneys, Level 43, 101 Collins Street,<br />
Melbourne, Victoria 3000, Australia<br />
(57) A method for obtaining site-specific recombination in an isolated<br />
eukaryotic cell comprising:<br />
- Providing an isolated eukaryotic cell that comprises a first recombination<br />
site and a second recombination site;<br />
- Contacting the first and second recombination site with a prokaryotic<br />
recombinase polypeptide resulting in recombination between the two sites;<br />
-The first recombination site is either a phage genomic recombination attachment<br />
site (attP) or a bacterial genomic recombination attachment<br />
site (attB) and the second recombination is either attP or attB, provided<br />
that when the first recombination site is attP the second recombination<br />
site is attB or vice versa;<br />
- The recombinase is a Mycobacterium tuberculosis phage recombinase<br />
or a M. smegmatis phage recombinase in particular the recombinases<br />
are phiRv1 or Bxb1 recombinase.<br />
The method also encompasses the use <strong>of</strong> pseudo attP and attB recombination<br />
sites as well as a third and fourth, and a fifth and sixth recombination<br />
site.<br />
Divisional filed as 583562<br />
(21) 556774 (22) 3 Jan 2006<br />
(54) Syrup composition comprising dexibupr<strong>of</strong>en as an active ingredient<br />
and method for the preparation there<strong>of</strong><br />
(86) PCT/KR2006/000016 (87) WO2006/073257<br />
(51) IPC2011.01:A61K9/08<br />
(71) HANMI PHARM. CO., LTD.<br />
(72) Woo, Jong Soo; Yi, Hong Gi; Jin, Ju Nam;<br />
(31) 05 0000222 (32) 3 Jan 2005 (33) KR<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed is a glycerin-free dexibupr<strong>of</strong>en syrup composition comprising:<br />
0.1 to 10 w/v percent <strong>of</strong> dexibupr<strong>of</strong>en ((S)-ibupr<strong>of</strong>en) having an average<br />
particle size ranging from 10 to 300 microns; 0.01 to 40 w/v percent<br />
<strong>of</strong> a viscosity controlling agent selected from the group consisting <strong>of</strong><br />
D-sorbitol solution, agar, sodium alginate, povidone, polyethylene glycol,<br />
hydroxyethylene cellulose and a mixture there<strong>of</strong>; 0.1 to 80 w/v percent <strong>of</strong><br />
a sweetener selected from the group consisting <strong>of</strong> sugar, high fructose,<br />
stevioside, dipotassium glycirhyzinate and a mixture there<strong>of</strong>; 0.01 to 10<br />
w/v percent <strong>of</strong> a suspending agent; 0.01 to 5 w/v percent <strong>of</strong> an emulsifier;<br />
and 0.01 to 5 w/v percent <strong>of</strong> a pH controlling agent, said composition<br />
having a viscosity ranging from 500 to 3,000 cPs and pH ranging from<br />
3.0 to 6.0. Also disclosed is a method to prepare said compostion.<br />
(21) 560283 (22) 18 Jan 2006<br />
(54) Rod-shaped light and light holder for marking a pylon<br />
(86) PCT/EP2006/000394 (87) WO2006/077084<br />
(51) IPC2011.01:F21S8/00; F03D11/00; F21V21/04; F21V33/00; F21V21/<br />
02<br />
(71) Aloys Wobben<br />
(72) Wobben, Aloys;<br />
(31) 05 05002650 (32) 19 Jan 2005 (33) DE<br />
(74) Pizzeys <strong>Patent</strong> and Trade Mark Attorneys, Level 2, Woden Plaza<br />
<strong>Office</strong>s, Woden Town Square, Woden, ACT 2606, Australia<br />
(57) A rod-shaped light 10 for a pylon comprises a substantially cylindrical<br />
rod-shaped holder at the first end <strong>of</strong> which lighting means and at the<br />
second end <strong>of</strong> which lighting means connections 15 are arranged. The<br />
rod-shaped light 10 is adapted to be fitted by means <strong>of</strong> the rod-shaped<br />
holder from the inside through a bore in the pylon wall 11 so that the<br />
lighting means radiate into the surrounding area <strong>of</strong> the pylon.<br />
(21) 560314 (22) 15 Feb 2006<br />
(54) Live attenuated rotavirus vaccine for oral administration<br />
(86) PCT/EP2006/001442 (87) WO2006/087205<br />
(51) IPC2011.01:A61K39/15; A61P1/00<br />
(71) GLAXOSMITHKLINE BIOLOGICALS S.A.<br />
(72) Vande Velde, Vincent;<br />
(31) 05 0503337 (32) 17 Feb 2005 (33) GB<br />
(74) HENRY HUGHES, 119-125 Willis Street, Wellington, New Zealand<br />
(57) A liquid rotavirus immunogenic composition suitable for oral administration<br />
to a human infant, comprising a rotavirus antigen, a sugar and a<br />
carboxylate. The composition has a pH <strong>of</strong> between pH 5.0 and pH 8.0<br />
and comprises less than 1 mM phosphate and the carboxylate is derived<br />
from a dicarboxylic acid with a pKa > 4. Suitable carboxylates are adipate,<br />
malate, succinate, malonate, glutarate, maleate, fumarate and tartarate.<br />
The composition is used as a vaccine for infants to prevent or treat gastroenteritis.<br />
(21) 560320 (22) 25 Jan 2006<br />
(54) Quinoxaline derivatives as antitumor agents<br />
(86) PCT/US2006/002717 (87) WO2006/081331<br />
(51) IPC2011.01:A61K31/495; C07D239/90; A61P35/00; C07D405/12;<br />
C07D409/12; G01N33/50,68<br />
(71) Prolexys Pharmaceuticals Inc.; Whitehead Institute for Biomedical<br />
Research; The Trustees <strong>of</strong> Columbia University in the City <strong>of</strong> New York<br />
(72) Becklin, Robert R; Chepanoske, Cindy Lou; Pelter, John M; Ql,<br />
Longwu; Robbins, Paul B; Sahasrabudhe, Sudhir R; Selliah, Robert;<br />
Simmons, Keith; Stockwell, Brent R; Venkat, Raj Gopal; Von Rechenberg,<br />
Moritz; Zhen, Eugene;<br />
(31) 05 647303 (32) 25 Jan 2005 (33) US<br />
(31) 06 762221 (32) 24 Jan 2006 (33) US<br />
(74) Shelston IP, Level 21, 60 Margaret Street, Sydney, NSW 2000, Australia<br />
(57) Disclosed are quinoxaline compounds <strong>of</strong> formula (I), or<br />
pharmaceutically acceptable salts there<strong>of</strong>, wherein W is a piperidine or a<br />
piperazine moiety and the rest <strong>of</strong> the substituents are disclosed within<br />
the specification. Also disclosed is the use <strong>of</strong> the said compound in the<br />
manufacture <strong>of</strong> a medicament for treating cancer in a mammal.<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 68 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(21) 560398 (22) 17 Feb 2006<br />
(54) Microwaveable film or sheet suitable for vacuum skin packaging applications<br />
and peelable microwaveable vacuum skin package obtained<br />
therewith<br />
(86) PCT/EP2006/001491 (87) WO2006/094617<br />
(51) IPC2011.01:B32B27/32; B65D75/30; C08L23/08<br />
(71) CRYOVAC, INC.<br />
(72) Riccio, Marina; Della Bianca, Serena;<br />
(31) 05101749 (32) 7 Mar 2005 (33) EP<br />
(31) 05108515 (32) 16 Sep 2005 (33) EP<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) The disclosure relates to a multi-layer film or sheet suitable for use in<br />
vacuum skin packaging (VSP) applications that has an outer layer comprising<br />
a blend <strong>of</strong> from about 8 to about 30 wt. % <strong>of</strong> modified polypropylene,<br />
from 0 to about 20 wt. % <strong>of</strong> polybutene and the complement to 100 wt. %<br />
<strong>of</strong> ionomer, wherein said modified polypropylene is a polypropylene that<br />
has been modified by grafting thereon an unsaturated carboxylic acid or<br />
a derivative there<strong>of</strong>. The disclosure also relates to a peelable VSP package<br />
where one <strong>of</strong> the webs has an outer sealing layer comprising a blend<br />
<strong>of</strong> from about 8 to 30 wt. % <strong>of</strong> modified polypropylene that has been<br />
modified by grafting thereon an unsaturated carboxylic acid or a derivative<br />
there<strong>of</strong>, from 0 to about 20 wt. % <strong>of</strong> polybutene and the complement<br />
to 100 wt. % <strong>of</strong> ionomer and the other web comprises an outer sealing<br />
layer having an ethylene homo- or copolymer-based surface, wherein<br />
said outer sealing layers are sealed to each other in one or more selected<br />
areas with a seal strength <strong>of</strong> from about 2.0 to about 4.0 N/25.4<br />
mm.<br />
(21) 560568 (22) 9 Dec 2005<br />
(54) Particulate compositions comprising phosphatidyl choline, diacyl glycerol<br />
or tocopherol, and a non-ionic stabilising amphiphile<br />
(86) PCT/GB2005/004745 (87) WO2006/077362<br />
(51) IPC2011.01:A61K9/127<br />
(71) CAMURUS AB<br />
(72) Johnsson, Markus; Tiberg, Fredrik;<br />
(31) 05 0501364 (32) 21 Jan 2005 (33) GB<br />
(31) 05 0507812 (32) 18 Apr 2005 (33) GB<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed is a particulate composition comprising:<br />
a) 5 to 50% <strong>of</strong> at least one phosphatidyl choline component b) 20 to 85%<br />
<strong>of</strong> at least one diacyl glycerol component, at least one tocopherol,or mixtures<br />
there<strong>of</strong>, andc) 1 to 40% <strong>of</strong> at least one non-ionic stabilising<br />
amphiphile consisting essentially <strong>of</strong> surfactants having a molecular weight<br />
below 8000 amu,wherein all parts are by weight relative to the sum <strong>of</strong> the<br />
weights <strong>of</strong> a+b+c and wherein the composition comprises particles <strong>of</strong> at<br />
least one non-lamellar phase structure or forms particles <strong>of</strong> at least one<br />
non-lamellar phase structure when contacted with an aqueous fluid.<br />
(21) 560613 (22) 17 Jan 2006<br />
(54) Water treatment with sand between aggregate layers, and distribution<br />
<strong>of</strong> water evenly at inlet<br />
(86) PCT/AU2006/000056 (87) WO2006/074529<br />
(51) IPC2011.01:B01D24/00,02,10,12,20; C02F1/00; E03F1/00; E03F5/<br />
00,14; B01D24/22<br />
(71) H2O World Wide Water Solutions Pty Ltd<br />
(72) Venville, Kevin John;<br />
(31) 05 900172 (32) 17 Jan 2005 (33) AU<br />
(31) 05 900228 (32) 20 Jan 2005 (33) AU<br />
(31) 05 905595 (32) 11 Oct 2005 (33) AU<br />
(74) H2O World Wide Water Solutions Pty Ltd, c/- H20 Pureplus Pty Ltd,<br />
Unit 2, No. 8 Riverland Drive, Loganholme, Queensland 4129, Australia<br />
(57) A sand filter apparatus (10) for treating water includes a filter retention<br />
vessel (16) having an outlet (18) from which filtrate can be supplied.<br />
An inlet arrangement (not shown fully) is in fluid communication with the<br />
filter retention vessel and is connectable to a supply <strong>of</strong> waste water. A<br />
filter is interposed between the inlet arrangement and the outlet. The<br />
filter includes two layers <strong>of</strong> aggregate (12) and a layer <strong>of</strong> sand (26) interposed<br />
between the two layers <strong>of</strong> aggregate. The sand is at least one <strong>of</strong>,<br />
or a mixture <strong>of</strong>, granite-based sand and substantially pure silica based<br />
sand. A distribution system (not shown) is connected to the inlet arrangement<br />
so that waste water from the inlet to the filter is distributed substantially<br />
evenly into the upper aggregate layer.<br />
(21) 560699 (22) 31 Aug 2006<br />
(54) Gravity gradiometer for measuring diagonal components <strong>of</strong> the gradient<br />
tensor<br />
(86) PCT/AU2006/001276 (87) WO2007/038825<br />
(51) IPC2011.01:G01V7/16<br />
(71) Technological Resources Pty Limited<br />
(72) Van Kann, Frank Joachim; Winterflood, John; Mann, Anthony Gordon;<br />
(31) 05 905524 (32) 6 Oct 2005 (33) AU<br />
(31) 05 906669 (32) 29 Nov 2005 (33) AU<br />
(31) 06 900193 (32) 13 Jan 2006 (33) AU<br />
(74) JAMES & WELLS, Level 12, KPMG Centre, 85 Alexandra Street,<br />
Hamilton, New Zealand<br />
(57) Disclosed is a system for measuring a gravity gradient tensor. The<br />
system comprises <strong>of</strong>: a gravity gradient sensor (40) with a pair <strong>of</strong> transversely<br />
arranged masses (41, 42) for use in a gravity gradiometer for<br />
measuring components <strong>of</strong> a gravity gradient tensor; a calibration sensor<br />
for sensing, at room temperature prior to cryogenic operation <strong>of</strong> the gravity<br />
gradiometer, whether one <strong>of</strong> the pair <strong>of</strong> masses associated with the<br />
calibration sensor is balanced; and an adjusting mechanism for adjusting<br />
the balance <strong>of</strong> the masses at room temperature prior to cryogenic<br />
operation <strong>of</strong> the gravity gradiometer. The calibration sensor comprises a<br />
resonant circuit having an inductor, and a capacitor which has a first<br />
plate formed by a surface <strong>of</strong> one <strong>of</strong> the masses and a second plate spaced<br />
from that surface <strong>of</strong> one <strong>of</strong> the masses; and an oscillator for receiving a<br />
signal from the resonant circuit and for producing an output signal indicative<br />
<strong>of</strong> the spacing between the first plate and the second plate. In<br />
use the calibration sensor produces a signal indicative <strong>of</strong> the balance <strong>of</strong><br />
the one <strong>of</strong> the pair <strong>of</strong> masses associated with the calibration sensor.<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 69 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(21) 560700 (22) 31 Aug 2006<br />
(54) Gravity Gradiometer with chevron shaped mass having a non-zero<br />
quadruple moment<br />
(86) PCT/AU2006/001272 (87) WO2007/038821<br />
(51) IPC2011.01:G01V7/16<br />
(71) Technological Resources Pty Limited<br />
(72) Van Kann, Frank Joachim; Winterflood, John;<br />
(31) 05 905524 (32) 6 Oct 2005 (33) AU<br />
(31) 05 906669 (32) 29 Nov 2005 (33) AU<br />
(31) 06 900193 (32) 13 Jan 2006 (33) AU<br />
(74) JAMES & WELLS, Level 12, KPMG Centre, 85 Alexandra Street,<br />
Hamilton, New Zealand<br />
(57) Disclosed is a gravity gradiometer for measuring components <strong>of</strong> a<br />
gravitational gradient tensor. The gradiometer comprises: a first housing<br />
(45); a first mass (41) forming one part <strong>of</strong> a pair <strong>of</strong> masses; and a first<br />
flexure web (59) located on a peripheral edge <strong>of</strong> the first mass. The<br />
flexure web pivotally connects the first mass with the first housing for<br />
movement there between in response to differences in a gravitational<br />
field so that signals can be produced indicative <strong>of</strong> components <strong>of</strong> the<br />
gravitational gradient tensor. The first mass has a non-zero quadruple<br />
moment with a centre <strong>of</strong> mass located at the flexure web and the first<br />
mass is chevron-shaped with first and second arms extending from the<br />
centre <strong>of</strong> mass.<br />
(21) 560701 (22) 31 Aug 2006<br />
(54) Gravity Gradiometer with a mounting having a three part mount connected<br />
by flexure webs<br />
(86) PCT/AU2006/001273 (87) WO2007/038822<br />
(51) IPC2011.01:G01V7/16<br />
(71) Technological Resources Pty Limited<br />
(72) Van Kann, Frank Joachim; Winterflood, John;<br />
(31) 05 905524 (32) 6 Oct 2005 (33) AU<br />
(31) 05 906669 (32) 29 Nov 2005 (33) AU<br />
(31) 06 900193 (32) 13 Jan 2006 (33) AU<br />
(74) JAMES & WELLS, Level 12, KPMG Centre, 85 Alexandra Street,<br />
Hamilton, New Zealand<br />
(57) Disclosed is a gravity gradiometer for measuring components <strong>of</strong> a<br />
gravity gradient tensor. The gradiometer comprises: a sensor (41, 42) for<br />
measuring the components <strong>of</strong> the gravity gradient tensor; and a mounting<br />
(5) for providing rotation about three substantially orthogonal axes,<br />
and for supporting the sensor. The sensor comprises a first mass (41)<br />
and a second mass (42) supported within respective first and second<br />
housings for movements relative to the housings in response to the gravitational<br />
field. The mounting comprises: a first mount (10); a second mount;<br />
and a first flexure web (33) for pivotally coupling the first and second<br />
mounts for pivotal movement about a first axis. The second mount has a<br />
first part (25), a second part (26) and a third part (27). The first part<br />
connects to the second part by a second flexure web (37) for pivotally<br />
coupling the first part to the second part for pivotal movement about a<br />
second axis orthogonal to the first axis. The third part is coupled to the<br />
second part by a third flexure web (35) for pivotally coupling the third part<br />
to the second part for pivotal movement about a third axis orthogonal to<br />
the first and second axes.<br />
(21) 560702 (22) 31 Aug 2006<br />
(54) Gravity Gradiometer with a mounting having a second mount with<br />
connectors which pass through cutouts in a first mount<br />
(86) PCT/AU2006/001271 (87) WO2007/038820<br />
(51) IPC2011.01:G01V7/16<br />
(71) Technological Resources Pty Limited<br />
(72) Van Kann, Frank Joachim; Winterflood, John;<br />
(31) 05 905524 (32) 6 Oct 2005 (33) AU<br />
(31) 05 906669 (32) 29 Nov 2005 (33) AU<br />
(31) 06 900193 (32) 13 Jan 2006 (33) AU<br />
(74) JAMES & WELLS, Level 12, KPMG Centre, 85 Alexandra Street,<br />
Hamilton, New Zealand<br />
(57) Disclosed is a gravity gradiometer for measuring components <strong>of</strong> a<br />
gravitational gradient tensor. The gradiometer comprises a sensor (40)<br />
for measuring the components <strong>of</strong> the gradient tensor and a mounting for<br />
supporting the sensor. The mounting comprises; a first mount, a second<br />
mount, and connectors. The first mount (10) has a base, a cylindrical<br />
hub protruding from the base, a peripheral wall (14) disposed around<br />
and spaced from the hub and provided with a plurality <strong>of</strong> circumferentially<br />
spaced cutouts (16), and a central core coaxial with the hub and<br />
attached to the hub by a first flexure web to provide for relative rotation<br />
between the core and base about a first axis. The second mount fits<br />
within the peripheral wall <strong>of</strong> the first mount and has first, second and<br />
third parts. The first and second parts connect via a second flexure web<br />
for relative rotation about a second axis orthogonal to the first axis. The<br />
second and third parts connect by a third flexure web for relative rotation<br />
about a third axis orthogonal to the first and second axes. The connectors<br />
(13) extend outwardly from the first part <strong>of</strong> the second mount through<br />
the cutouts in the peripheral wall <strong>of</strong> the first mount for connecting the<br />
mounting to an external platform. The third part <strong>of</strong> the second mount is<br />
attached to the core <strong>of</strong> the first mount and the sensor is connected to the<br />
base <strong>of</strong> the first mount. Hence the sensor is rotatable with the base <strong>of</strong><br />
the first mount about all three orthogonal axes.<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 70 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(21) 560836 (22) 19 Jan 2006<br />
(54) Food preservation systems including a multi phase bacterial inhibition<br />
food pad<br />
(86) PCT/US2006/001977 (87) WO2006/078868<br />
(51) IPC2011.01:A23B4/20; B65D81/28; A23B4/14; B65D81/26<br />
(71) Paper Pak Industries<br />
(72) Etchells, Marc D; Versteylen, Sayandro;<br />
(31) 05 645856 (32) 21 Jan 2005 (33) US<br />
(74) JAMES & WELLS, Level 12, KPMG Centre, 85 Alexandra Street,<br />
Hamilton, New Zealand<br />
(57) An absorbent, bacterial inhibition food pad comprises two or more<br />
layers 32, 34 <strong>of</strong> absorbent or superabsorbent tissue that can absorb up<br />
to 50 grams <strong>of</strong> a liquid purge from a food product. The absorbent media/<br />
material includes a CO2 generating system that modifies the atmosphere<br />
in a food package that includes the food pad, and one or more bacterial<br />
inhibitors that may possess bacteriostatic and/or bactericidal properties.<br />
The CO2 generating system has a bacteriostatic effect on bacteria on<br />
the surface <strong>of</strong> the food product, while the bacterial inhibitors have a bacteriostatic<br />
effect on bacteria in the liquid purge. The food pad enhances<br />
the shelf life, food safety, and appearance <strong>of</strong> a food product.<br />
Divisional filed as 590336<br />
(21) 560849 (22) 6 Feb 2006<br />
(54) Compounds comprising linked heteroaryl moieties and their use as<br />
novel umami flavor modifiers, tastants and taste enhancers for comestible<br />
compositions<br />
(86) PCT/US2006/003956 (87) WO2006/084186<br />
(51) IPC2011.01:A23L1/231,226; C07D401/12; C07D405/14; C07D403/<br />
14; C07D407/14; C07D409/12<br />
(71) SENOMYX, INC.<br />
(72) Tachdjian, Catherine; Lebl-Rinnova, Marketa; Wallace, David;<br />
(31) 05 650029 (32) 4 Feb 2005 (33) US<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) Disclosed is a compound <strong>of</strong> Formula (IA) or a comestibly acceptable<br />
salt there<strong>of</strong>, wherein n', n", hAr1 and hAr2 is defined in the specification.<br />
Also disclosed is a composition comprising said compound and a method<br />
for modulating savory taste comprising said compound.<br />
(21) 560881 (22) 13 Mar 2006<br />
(54) Throwing and catching apparatus comprising at least one scoop element<br />
with flexible ribs<br />
(86) PCT/GB2006/000898 (87) WO2006/100435<br />
(51) IPC2011.01:A63B59/02<br />
(71) ROBERT GEORGE ELDRIDGE<br />
(72) Eldridge, Robert George;<br />
(31) 05 0505951 (32) 23 Mar 2005 (33) GB<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) An apparatus (10) for throwing and catching a ball is disclosed. The<br />
apparatus (10) comprises an elongate shaft member (11) and at least<br />
one scoop element (14). The scoop element (14) includes at least one<br />
flexible member comprising a plurality <strong>of</strong> flexible ribs that extend perpendicular<br />
to a longitudinal axis associated with the scoop element (14).<br />
The resilient feature <strong>of</strong> ribs allows absorption <strong>of</strong> energy from the impact<br />
<strong>of</strong> a ball so that this energy is not transferred to the ball which could<br />
otherwise bounce out <strong>of</strong> the scoop element (14).<br />
(21) 560914 (22) 7 Apr 2006<br />
(54) Cellulose solutions in ionic liquids based upon imidazolium cations<br />
(86) PCT/EP2006/061422 (87) WO2007/057235<br />
(51) IPC2011.01:C08B1/00; C08L1/02; C07D233/58<br />
(71) BASF Aktiengesellschaft<br />
(72) Maase, Matthias; Stegmann, Veit;<br />
(31) 05 05017715 (32) 15 Apr 2005 (33) DE<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) Disclosed is a solution comprising cellulose and an ionic liquid comprising<br />
anions and cations as solvent, wherein the cations comprise at<br />
least one atom selected from the group consisting <strong>of</strong> nitrogen, oxygen,<br />
sulfur and phosphorus which is present in protonated form, and wherein<br />
the ionic liquid comprises at least one imidazolium cation <strong>of</strong> formula (IVe)<br />
and oligomers comprising this structure, where the radical R is hydrogen;<br />
and the radicals R1 to R4 are each, independently <strong>of</strong> one another,<br />
hydrogen, or unbranched or branched C1-C18 alkyl which is unsubstituted.<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 71 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(21) 560964 (22) 10 Apr 2006<br />
(54) 1H-Quinazoline-2,4-diones and their use as AMPA-receptor ligands<br />
(86) PCT/EP2006/003251 (87) WO2006/108591<br />
(51) IPC2011.01:C07D239/96; A61K31/517; A61P25/08,18; C07D207/32;<br />
C07D231/12; C07D237/08; C07D249/06; C07D307/16,54; C07D309/12;<br />
C07D401/04; C07D403/04; C07D405/04; C07D413/04<br />
(71) Novartis AG<br />
(72) Allgeier, Hans; Auberson, Yves; Floersheim, Philipp; Guibourdenche,<br />
Christel; Froestl, Wolfgang; Kallen, Jorg; Mattes, Henri; Nozulak, Joachim;<br />
Orain, David; Renaud, Johanne; Carcache, David; Koller, Manuel;<br />
(31) 05 0507298 (32) 11 Apr 2005 (33) GB<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) Disclosed are 1H-quinazoline-2,4-diones <strong>of</strong> formula (I) wherein R1<br />
represents CF3 or iso-propyl and R2 represents an optionally substituted<br />
heterocyclyl, such as N-[7-Isopropyl-6-(2-methyl-2H-pyrazol-3-yl)-<br />
2,4-dioxo-1,4-dihydro-2H-quinazolin-3-yl]methanesulfonamide<br />
or a salt there<strong>of</strong>. Also disclosed is the use <strong>of</strong> the<br />
compounds for the treatment <strong>of</strong> conditions mediated by the AMPA receptor<br />
such as epilepsy and schizophrenia.<br />
Divisional filed as 590463<br />
(21) 560979 (22) 6 Feb 2006<br />
(54) Selective direction <strong>of</strong> air in ro<strong>of</strong> space out <strong>of</strong> or into the building<br />
(86) PCT/AU2006/000146 (87) WO2006/081630<br />
(51) IPC2011.01:E04B7/18; E04D13/18,17; F24F7/02<br />
(71) Terrance Robert Oaten<br />
(72) Oaten, Terrance Robert;<br />
(31) 05 900509 (32) 4 Feb 2005 (33) AU<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) A ro<strong>of</strong> assembly for a building which includes a ro<strong>of</strong>, a ro<strong>of</strong> space 2 in<br />
heat exchange relationship with a section 8 <strong>of</strong> the ro<strong>of</strong>, a chamber 3<br />
placed on the ro<strong>of</strong> and fans 15 for causing airflow within the ro<strong>of</strong> space<br />
2. The chamber has one or more first openings 5 that allow airflow from<br />
within the ro<strong>of</strong> space to outside the building to cool the building, and one<br />
or more second openings 7 that allow air flow from the ro<strong>of</strong> space 2 to a<br />
living space <strong>of</strong> the building. Airflow is controlled by selectively opening<br />
and closing the first and second openings.<br />
(21) 561062 (22) 8 Mar 2006<br />
(54) Rechargeable battery and method for its operation<br />
(86) PCT/EP2006/002130 (87) WO2006/094785<br />
(51) IPC2011.01:H02J7/00<br />
(71) AXEL MUNTERMANN<br />
(72) Muntermann, Axel;<br />
(31) 05 05011081 (32) 8 Mar 2005 (33) DE<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) A rechargeable battery, a method for operation <strong>of</strong> a rechargeable<br />
battery, and a rechargeable battery arrangement, is disclosed. The rechargeable<br />
battery is provided for operation with an external voltage,<br />
which is applied at least at times to the output <strong>of</strong> the rechargeable battery,<br />
and is below the output voltage <strong>of</strong> the rechargeable battery when in<br />
its fully charged state. The rechargeable battery comprises: (a) at least<br />
one chargeable electrochemical cell; (b) an electrical connection to the<br />
output <strong>of</strong> the rechargeable-battery for inputting and/or outputting electrical<br />
energy; (c) a housing which surrounds the at least one chargeable<br />
electrochemical cell; and (d) a control circuit for controlling the charging<br />
process <strong>of</strong> the rechargeable battery and/or the production <strong>of</strong> the rechargeable-battery<br />
voltage at the output <strong>of</strong> the rechargeable battery. The control<br />
circuit is adapted to disconnect the rechargeable battery voltage from<br />
the output <strong>of</strong> the rechargeable battery at cyclic time intervals in order to<br />
check whether the external voltage is applied to the output <strong>of</strong> the rechargeable<br />
battery.<br />
Divisional filed as 590185<br />
(21) 561117 (22) 16 Mar 2006<br />
(54) Working platform for interior <strong>of</strong> tower such as wind power tower, with<br />
scissors carrier structure and overlapping plates<br />
(86) PCT/EP2006/060785 (87) WO2006/097505<br />
(51) IPC2011.01:E04G1/36<br />
(71) Aloys Wobben<br />
(72) Wobben, Aloys;<br />
(31) 05 05012497 (32) 16 Mar 2005 (33) DE<br />
(74) Pizzeys <strong>Patent</strong> and Trade Mark Attorneys, Level 2, Woden Plaza<br />
<strong>Office</strong>s, Woden Town Square, Woden, ACT 2606, Australia<br />
(57) The disclosure relates to a working platform to be used inside a towertype<br />
building. The aim is to design a working platform, which can be<br />
used when the top section <strong>of</strong> the tower is closed by a structure. For this<br />
purpose, the inventive working platform consists <strong>of</strong> a bearing structure in<br />
the form <strong>of</strong> scissors lattice frame and a platform placed thereon. Said<br />
bearing structure in the form <strong>of</strong> scissors lattice frame enables the inventive<br />
working platform to be adapted to various internal diameters <strong>of</strong> the<br />
tower-type building, thereby covering the entire tower cross section. The<br />
bearing structure in the form <strong>of</strong> scissors lattice frame also makes it possible<br />
to release the working platform from the tower wall and to fix it in<br />
the other part <strong>of</strong> the tower having the different cross section.<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 72 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(21) 561145 (22) 1 Feb 2006<br />
(54) Pyrazolylaminopyridine derivatives useful as kinase inhibitors<br />
(86) PCT/GB2006/000334 (87) WO2006/082392<br />
(51) IPC2011.01:C07D401/14; A61K31/4439; A61P35/00; C07D401/12;<br />
C07D405/14; C07D409/14; C07D413/14<br />
(71) ASTRAZENECA AB<br />
(72) Davies, Audrey; Lamb, Michelle; Lyne, Paul; Mohr, Peter; Wang, Bin;<br />
Wang, Tao; Yu, Dingwei;<br />
(31) 05 653329 (32) 16 Feb 2005 (33) US<br />
(31) 05 721633 (32) 29 Sep 2005 (33) US<br />
(31) 05 650053 (32) 4 Feb 2005 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed is a compound <strong>of</strong> formula (I) wherein one <strong>of</strong> X1, X2, X3 and<br />
X4 is =N-, the other three are independently selected from =CR8, =CR9and<br />
=CR10-, A is a direct bond or optionally substituted C1-2alkylene,<br />
Ring C is carbocyclyl or heterocyclyl, and wherein the rest <strong>of</strong> the<br />
substituents are disclosed within the specification.<br />
Also disclosed is a process for preparing a compound <strong>of</strong> formula (I). Also<br />
disclosed is the use <strong>of</strong> a compound <strong>of</strong> formula (I) in the manufacture <strong>of</strong> a<br />
medicament for use in the inhibition <strong>of</strong> Trk activity, for the treatment or<br />
prophylaxis <strong>of</strong> cancer or for use in the production <strong>of</strong> an anti-proliferative<br />
effect.<br />
(21) 561232 (22) 20 Jun 2006<br />
(54) An attachment plate <strong>of</strong> an spinal disc comprising v-shaped self-tapping<br />
fixing ribs<br />
(86) PCT/EP2006/005910 (87) WO2006/136373<br />
(51) IPC2011.01:A61F2/44<br />
(71) CERVITECH, INC.<br />
(72) Keller, Arnold;<br />
(31) 05 05013517 (32) 22 Jun 2005 (33) EP<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) An attachment plate forming part <strong>of</strong> an intervertebral prosthesis that<br />
includes two attachment plates is disclosed. The attachment plate comprises<br />
an attachment surface with fixing projections. The attachment<br />
surface is configured for attachment to an adjacent vertebral body, which<br />
has a base surface configured to bear on a endplate <strong>of</strong> the adjacent<br />
vertebral body. The fixing projections rise from the base surface wherein<br />
the fixing projections are arranged symmetrically about a medial plane in<br />
at least two rows with an interspace opening between the rows. The<br />
rows extend outwardly and obliquely in a V-shape with respect to an<br />
implantation direction. The fixing projections are configured with a first<br />
limit surface formed by a lateral-facing side surface, a second limit surface<br />
formed by a medial-facing side surface, a third limit surface formed<br />
by a steep ventral-facing surface, and a fourth limit surface formed by an<br />
inclined dorsal facing surface. The fixing projections are self tapping and<br />
configured to penetrate into the endplate <strong>of</strong> the adjacent vertebral body.<br />
(21) 561237 (22) 24 Mar 2006<br />
(54) 8-Phenyl-7,8-dihydropyrido[2,3-d]pyrimidin-7-ones and their use as<br />
pharmaceuticals<br />
(86) PCT/US2006/010855 (87) WO2006/104915<br />
(51) IPC2011.01:A61K31/519,5365; C07D471/04; C07D487/04; C07D413/<br />
14<br />
(71) GLAXO GROUP LIMITED<br />
(72) Boehm, Jeffrey C.; Callahan, James Francis; Cooper, Anthony William<br />
James; Livia, Stefano; Nevins, Neysa; Wan, Zehong; Norton, Beth A;<br />
(31) 05 665315 (32) 25 Mar 2005 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed are the compounds:<br />
3-[2-{[3-(diethylamino)propyl]amino}-8-(2,6-difluorophenyl)-7-oxo-7,8dihydropyrido[2,3-d]pyrimidin-4-yI]-5-fluoro-4-methyl-N-(1methylethyl)benzamide;N-cyclopropyl-3-[2-{[3-(diethylamino)propyl]amino}-8-(2,6-difluorophenyl)-7-oxo-7,8-dihydropyrido[2,3d]pyrimidin-4-yl]-5-fluoro-4-methylbenzamide,<br />
and 3-{8-(2,6difluorophenyl)-2-[(1H-imidazol-2-ylmethyl)amino]-7-oxo-7,8dihydropyrido[2,3-d]pyrimidin-4-yI}-4-methyl-N-1,3-thiazol-2-yIbenzamide.<br />
Also more generally disclosed are compounds <strong>of</strong> the pictured formula where<br />
the substituents are as described in the specification. Also disclosed are<br />
the use <strong>of</strong> the compounds in medicaments.<br />
Divisional filed as 590761<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 73 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(21) 561323 (22) 10 Feb 2006<br />
(54) Acetic acid production methods incorporating at least one metal salt<br />
as a catalyst stabilizer<br />
(86) PCT/US2006/004772 (87) WO2006/091397<br />
(51) IPC2011.01:C07C51/12; C07C53/08<br />
(71) Celanese International Corporation<br />
(72) Torrence, G. Paul;<br />
(31) 05 67265 (32) 24 Feb 2005 (33) US<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) A process for the production <strong>of</strong> acetic acid, by a catalytic carbonylation<br />
reaction, comprising reacting methanol in a reaction mixture, in the presence<br />
<strong>of</strong> carbon monoxide and a rhodium-based catalyst system comprising:<br />
(i) rhodium in a concentration <strong>of</strong> at least 300 ppm;<br />
(ii) a halogen promoter selected from hydrogen iodide and an organic<br />
iodide; (iii) an iodide salt co-promoter in the form <strong>of</strong> a soluble salt <strong>of</strong> alkali<br />
metal or alkaline earth metal or quaternary ammonium or phosphonium<br />
salt at a concentration that generates an iodide ion concentration <strong>of</strong> greater<br />
than 3 wt.% <strong>of</strong> the reaction mixture; and (iv) a metal salt stabilizer selected<br />
from the group consisting <strong>of</strong> ruthenium salts, tin salts, and mixtures<br />
there<strong>of</strong>; wherein the reaction mixture comprises from 0.1 wt.% to<br />
14 wt.% water, and wherein the ruthenium salts, tin salts, and mixtures<br />
there<strong>of</strong> are present in the reaction mixture in a molar ratio <strong>of</strong> combined<br />
ruthenium and tin to rhodium <strong>of</strong> from 0.1:1 to 20:1.<br />
(21) 561327 (22) 7 Feb 2006<br />
(54) Lighting system having magnetically attached plates<br />
(86) PCT/GB2006/050030 (87) WO2006/085117<br />
(51) IPC2011.01:F21V21/35,096; F21V23/06<br />
(71) COHDA DESIGN LIMITED<br />
(72) Liddle, Richard;<br />
(31) 05 0502725 (32) 10 Feb 2005 (33) GB<br />
(74) PHILLIPS ORMONDE FITZPATRICK, 367 Collins Street, Melbourne,<br />
Victoria 3000, Australia<br />
(57) Disclosed is a movable lighting element using magnetic plates. The<br />
lighting element (1) comprises at least one light (3), means for delivering<br />
electricity to each light (12, 13), a pair <strong>of</strong> spaced apart plates (2, 2’), at<br />
least one magnet (4) located between the plates, and biasing means (8)<br />
for biasing the plates apart. The magnet is attached to a first plate (2) <strong>of</strong><br />
the pair <strong>of</strong> plates and movable relative to a second (2’) <strong>of</strong> the pair <strong>of</strong><br />
plates. The first plate is adapted to move towards the second plate against<br />
a biasing force generated by the biasing means, when a magnet having<br />
a polarity opposing that <strong>of</strong> the magnet attached to the first plate is presented<br />
up to and aligned therewith.<br />
(21) 561373 (22) 27 Feb 2006<br />
(54) Composite secondary carpet backing, method <strong>of</strong> manufacture there<strong>of</strong>,<br />
and carpet made therefrom<br />
(86) PCT/US2006/006831 (87) WO2006/093861<br />
(51) IPC2011.01:B32B33/00; D04H1/48; D04H13/00; A47G27/00,02<br />
(71) PROPEX FABRICS INC<br />
(72) Gardner, Hugh C; Baker, Thomas L; Moon, Richard C; White, Robert<br />
J; Haire, James E; Galpin, Charles W.;<br />
(31) 05 657042 (32) 28 Feb 2005 (33) US<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) A carpet 700 consisting <strong>of</strong> a primary backing 705, face yarn consisting<br />
<strong>of</strong> a plurality <strong>of</strong> filaments tufted through the primary backing, and a<br />
binder layer 710 adhering a stitched side <strong>of</strong> the primary backing 705 to a<br />
secondary backing 300, the secondary backing 300 consisting <strong>of</strong> a woven<br />
fabric layer 405 having a flat weave which comprises at least one <strong>of</strong><br />
a plain, satin, and twill weave construction <strong>of</strong> tape yarns in a warp direction<br />
interwoven with multifilament yarns in a filling direction, the woven<br />
fabric layer 405 having an open area <strong>of</strong> about 15% or less, the multifilament<br />
yarns having a thickness that is at least three times the thickness <strong>of</strong><br />
warp tapes such that gaps are formed at crossover regions formed by<br />
the multifilament yarns and warp tapes, and a fibrous layer 510, where<br />
the fibrous layer 510 weighs between about 0.5 osy (0.169 gsm) and<br />
about 10 osy (3.39 gsm), and where at least a portion <strong>of</strong> the fibers 410<br />
have penetrated through the woven fabric layer 405 and extend outward<br />
from a side there<strong>of</strong> and wherein the secondary backing 300 has an air<br />
permeability <strong>of</strong> greater than about 220 cfm/sq ft (67 m3/min/m2).<br />
(21) 561407 (22) 15 Mar 2006<br />
(54) Sequestering agent for micronutrient fertilisers<br />
(86) PCT/AU2006/000334 (87) WO2006/096912<br />
(51) IPC2011.01:C05G3/00; C05D9/02<br />
(71) ADELAIDE RESEARCH AND INNOVATION PTY LTD; COMMON-<br />
WEALTH SCIENTIFIC AND INDUSTRIAL RESEARCH ORGANISATION<br />
(72) McLaughlin, Mike; Stacey, Samuel; Lombi, Enzo;<br />
(31) 2005 901235 (32) 15 Mar 2005 (33) AU<br />
(74) COLLISON & CO, 117 King William Street, Adelaide, South Australia<br />
5000, Australia<br />
(57) Disclosed is a method <strong>of</strong> increasing the uptake <strong>of</strong> micronutrients by a<br />
plant which comprises applying to an area <strong>of</strong> a plant, or soil/substrate<br />
surrounding the plant, an effective amount <strong>of</strong> a plant fertiliser composition<br />
comprising a surfactant for forming coordinate bonds with the<br />
micronutrients, the surfactant transporting the micronutrients across a<br />
membrane <strong>of</strong> the plant and releasing the micronutrients for use by the<br />
plant wherein the surfactant is a rhamnolipid with the general formula<br />
(III), wherein the substituents are as defined in the specification.<br />
(21) 561438 (22) 24 Mar 2006<br />
(54) Novel substituted 1,5,7-trisubstituted-3,4-dihydro-pyrimido[4,5d]pyrimidin-2-[1H]-one<br />
compounds, pharmaceutical compositions, and use<br />
in the manufacture <strong>of</strong> medicines<br />
(86) PCT/US2006/010792 (87) WO2006/104889<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 74 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(51) IPC2011.01:C07D475/00; C07D239/47; C07D243/08; C07D413/<br />
12,14; A61K31/519,535,55,5513<br />
(71) Glaxo Group Limited<br />
(72) Callahan, James Francis; Wan, Zehong; Yan, Hongxing;<br />
(31) 05 665347 (32) 25 Mar 2005 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed are the following three compounds:<br />
3-[2-{[3-(diethylamino)propyl]amino}-8-(2,6-difluorophenyl)-7-oxo-5,6,7,8tetrahydropyrimido[4,5-d]pyrimidin-4-yl]-4-methyl-N-propylbenzamide;3-[8-(2,6-difluorophenyl)-2-(4-methyl-1,4'-bipiperidin-1'-yl)-7-oxo-5,6,7,8tetrahydropyrimido[4,5-d]pyrimidin-4-yl]-4-methyl-N-(1methylethyl)benzamide;<br />
and 3-{8-(2,6-difluorophenyl)-2-[4-(4-methyl-1piperazinyl)-1-piperidinyl]-7-oxo-5,6,7,8-tetrahydropyrimido[4,5d]pyrimidin-4-yI}-4-methyl-N-(1-methyl<br />
ethyl)benzamide, and salts there<strong>of</strong>.<br />
Also more generally disclosed are compound <strong>of</strong> the pictured formulas,<br />
where the substituents and variables are as defined in the specification.<br />
Also disclosed is the use <strong>of</strong> the above compound to treat CSBP/RK/p38<br />
kinase mediated diseases such as asthma, adult respiratory distress<br />
syndrome, chronic pulmonary inflammatory disease, and chronic obstructive<br />
pulmonary disease (COPD).<br />
Divisional filed as 590846<br />
(21) 561541 (22) 15 Mar 2006<br />
(54) Compositions <strong>of</strong> ethylene/alpha-olefin multi-block interpolymer suitable<br />
for films<br />
(86) PCT/US2006/009408 (87) WO2006/101930<br />
(51) IPC2011.01:C08F297/08; C08F2/38; C08F4/646<br />
(71) DOW GLOBAL TECHNOLOGIES INC.<br />
(72) Cheung, Yunwa Wilson; Demirors, Mehmet; Jain, Pradeep; Fuchs,<br />
David Winn; Cham, Pak-meng;<br />
(31) 2005 008917 (32) 17 Mar 2005 (33) US<br />
(31) 05 718198 (32) 16 Sep 2005 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed is a film (for use a stretchwrap packaging <strong>of</strong> fresh food for<br />
example) which comprises at least one ethylene/a-olefin interpolymer<br />
prepared using a chain shuttling agent in the polymerization, wherein the<br />
ethylene/a-olefin interpolymer is a multi-block interpolymer comprising<br />
at least 50 mole percent ethylene, has a polydispersity (Mw/Mn) from<br />
about 1.7 to about 3.5 and which also has the specific physical characteristics<br />
as defined herein.<br />
(21) 561552 (22) 22 Feb 2006<br />
(54) Low distortion interlayer for multiple layer glass panels<br />
(86) PCT/US2006/006357 (87) WO2006/091707<br />
(51) IPC2011.01:B32B17/10; B29D7/01<br />
(71) Solutia Inc.<br />
(72) Yacavone, Vincent;<br />
(31) 05 061778 (32) 22 Feb 2005 (33) US<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) A polymer sheet, comprising: poly(vinyl butyral); and, a plasticizer,<br />
wherein said polymer sheet has a surface with a waviness index <strong>of</strong> less<br />
than 20,000 square micrometers, an Rz value <strong>of</strong> at least 20 micrometers,<br />
and a permanence <strong>of</strong> between 10 and 95 percent is disclosed.<br />
The disclosure also relates to a method <strong>of</strong> producing a multiple layer<br />
interlayer, comprising the steps <strong>of</strong>: forming a first polymer sheet comprising<br />
poly(vinyl butyral) and a plasticizer, wherein said first polymer<br />
sheet has a first surface and a second surface and wherein said first<br />
surface has a waviness index <strong>of</strong> less than 20,000 square micrometers,<br />
an Rz value <strong>of</strong> at least 20 micrometers, and a permanence <strong>of</strong> between<br />
10 and 95; disposing a layer <strong>of</strong> polymer film in contact with said first<br />
surface <strong>of</strong> said first polymer sheet to form a stack; and, laminating said<br />
stack.<br />
(21) 561649 (22) 28 Mar 2006<br />
(54) Methods, compositions, and formulations for preventing or reducing<br />
adverse effects in a patient<br />
(86) PCT/US2006/011422 (87) WO2006/105167<br />
(51) IPC2011.01:A61K31/70,7056<br />
(71) PERICOR THERAPEUTICS, INC.<br />
(72) Mangano, Dennis T;<br />
(31) 05 666071 (32) 28 Mar 2005 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed is a use <strong>of</strong> 5-amino-1-beta-D-(5-benzylamino-5-deoxy-1beta-D-rib<strong>of</strong>uranosyl)imidazole-4-carboxamide,5-amino-1-(5-amino-5deoxy-beta-D-rib<strong>of</strong>uranosyl)imidazole-4-N-[(4chlorophenyl)methyl]carboxamide,<br />
or a salt there<strong>of</strong> in the manufacture<br />
<strong>of</strong> a medicament for reducing the incidence <strong>of</strong> mortality in patients in<br />
need there<strong>of</strong>, wherein said patients have decreased left ventricular function<br />
having an ejection fraction that is less than 30%, the medicament is<br />
also suitable for treating a patient with decreased left ventricular function<br />
having an ejection fraction that is less than 30%.<br />
(21) 561664 (22) 24 Feb 2006<br />
(54) Trans carotenoids, their synthesis, formulation and uses<br />
(86) PCT/US2006/006422 (87) WO2006/104610<br />
(51) IPC2011.01:C07C59/185<br />
(71) Diffusion Pharmaceuticals LLC<br />
(72) Gainer John L; Lanz, Marc;<br />
(31) 05 655422 (32) 24 Feb 2005 (33) US<br />
(74) CULLEN & CO, Level 32, 239 George Street, Brisbane, QLD 4001,<br />
Australia<br />
(57) Disclosed is a pharmaceutical composition comprising:<br />
(i) a bipolar trans carotenoid salt having the formula:<br />
YZ-TCRO-ZY<br />
where:<br />
Y = a cation which can be the same or different, Z = a polar group which<br />
can be the same or different and which is associated with the cation, and<br />
TCRO = a linear trans carotenoid skeleton with conjugated carbon-carbon<br />
double bonds and single bonds, and having pendant groups X,<br />
wherein the pendant groups X, which can be the same or different, are a<br />
linear or branched hydrocarbon group having 10 or less carbon atoms,<br />
or a halogen, and (ii) a cyclodextrin.These compositions are useful in<br />
improving diffusivity <strong>of</strong> oxygen between red blood cells and body tissues<br />
in mammals including humans, and are suitable for the treatment <strong>of</strong> cancer<br />
selected from the group consisting <strong>of</strong> glioblastomas, squamous cell<br />
carcinomas, melanomas, lymphomas, sarcomas, sarcoids, osteosarcomas,<br />
skin cancer, breast cancer, head and neck cancer, gynecological<br />
cancer, urological and male genital cancer, bladder cancer, prostate cancer,<br />
bone cancer, cancers <strong>of</strong> the endocrine glands, cancers <strong>of</strong> the alimentary<br />
canal, cancers <strong>of</strong> the major digestive glands/organs, CNS cancer,<br />
and lung cancer.<br />
(21) 561677 (22) 3 Apr 2006<br />
(54) (S)-N-[2-(1,6,7,8-tetrahydro-2H-indeno[5,4-b]furan-8yl)ethyl]propionamide,<br />
and its use for treating depression and anxiety neurosis<br />
(86) PCT/JP2006/307047 (87) WO2006/107019<br />
(51) IPC2011.01:C07D307/77; A61K31/343; A61K45/00; A61P25/<br />
20,22,24,28; A61P43/00<br />
(71) Takeda Pharmaceutical Company Limited<br />
(72) Hirai, Keisuke; Miyamoto, Masaomi;<br />
(31) 2005 107674 (32) 4 Apr 2005(33) JP<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) Disclosed is a pharmaceutical composition for prevention or treatment<br />
<strong>of</strong> depression or anxiety disorders, which comprises synergistically<br />
effective amounts <strong>of</strong> (S)-N-[2-(1, 6,7, 8-tetrahydro-2H-indeno[5, 4-b] furan-<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 75 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
8-yl)ethyl]propionarnide in combination with one or more drugs selected<br />
from other antidepressants and antianxiety drugs, consisting <strong>of</strong> SSRI<br />
and benzodiazepine antianxiety drugs, such as Fluoxetine, Sertraline,<br />
Paroxetine, Diazepam, Alprazolam and Oxazolam.<br />
(21) 561843 (22) 27 Apr 2005<br />
(54) Adding a production additive to an aqueous dispersion <strong>of</strong> calcined<br />
gypsum with the ratio <strong>of</strong> viscosity between the two is between 10:1 to 2:1<br />
(86) PCT/US2005/014504 (87) WO2006/115497<br />
(51) IPC2011.01:C04B11/00<br />
(71) UNITED STATES GYPSUM COMPANY<br />
(72) Wittbold, James R; Song, W David;<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed is a method <strong>of</strong> introducing a production additive to a postmixer<br />
aqueous dispersion <strong>of</strong> calcined gypsum. The method comprises<br />
the steps <strong>of</strong>: forming an aqueous dispersion <strong>of</strong> calcined gypsum in a<br />
mixer chamber; discharging the aqueous dispersion into a discharge<br />
apparatus; introducing the production additive into the aqueous dispersion<br />
within the discharge apparatus. The ratio <strong>of</strong> the viscosity <strong>of</strong> the production<br />
additive to the aqueous dispersion is between about 10:1 to about<br />
2:1.<br />
(21) 561849 (22) 29 Mar 2006<br />
(54) A manual vascular compression device with a rigid convex bottom<br />
pad<br />
(86) PCT/US2006/011395 (87) WO2006/105153<br />
(51) IPC2011.01:A61B17/00,08; A61D1/00; A61B17/03<br />
(71) MARINE POLYMER TECHNOLOGIES, INC.<br />
(72) Finkielsztein, Sergio; Finkielsztein, Marco; Vournakis, John N;<br />
(31) 05 92369 (32) 29 Mar 2005 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) A vascular compression apparatus for applying pressure to tissue in<br />
proximity to a puncture site and a blood vessel, comprises a handle 14,<br />
a shaft 12 extending generally perpendicularly from the handle 14, and a<br />
rigid pad 11 having a top side 19 and a convex bottom side 18, which<br />
makes contact with the body surface. The device is configured to allow<br />
the user to rock the convex pad 11 proximally and distally.<br />
(21) 562130 (22) 7 Mar 2006<br />
(54) Optical phase conjugation laser diode with retro-reflecting elements<br />
(86) PCT/US2006/007817 (87) WO2007/027196<br />
(51) IPC2011.01:H01S3/13<br />
(71) OPC Laser Systems L.L.P.<br />
(72) Henrichs, Joseph Reid;<br />
(31) 05 74342 (32) 7 Mar 2005 (33) US<br />
(74) PHILLIPS ORMONDE FITZPATRICK, 367 Collins Street, Melbourne,<br />
Victoria 3000, Australia<br />
(57) Disclosed is an optical phase conjugating laser diode. The diode includes<br />
a first reflector (168), a second reflector (165), and a gain-medium<br />
(160, 161, 162) sandwiched between the first and second reflectors.<br />
The second reflector is used to provide for a partial reflection and<br />
laser-emission output, and the gain medium is used to provide for a stimulated-emission<br />
and amplification. The first reflector comprises a phase-<br />
conjugating array, the array comprising a plurality <strong>of</strong> retro-reflecting elements.<br />
The first reflector is used to provide for an optical phase conjugation.<br />
(21) 562226 (22) 13 Mar 2006<br />
(54) Broadband land mobile antenna<br />
(86) PCT/IL2006/000324 (87) WO2006/097919<br />
(51) IPC2011.01:H04B1/02<br />
(71) Galtronics Ltd.<br />
(72) Babitsky, Gennady; Martiskainen, Matti;<br />
(31) 05 661795 (32) 14 Mar 2005 (33) US<br />
(74) SPRUSON & FERGUSON, St Martins Tower, Level 35, 31 Market<br />
Street, Sydney, New South Wales 2000, Australia<br />
(57) Disclosed is a monopole antenna. The antenna includes a helical<br />
radiating element (126) including a first longitudinal portion having a first<br />
winding pitch (128) and a second longitudinal portion having a second<br />
winding pitch (130). The antenna also includes a cylindrical radiating<br />
element (134) generally coaxial with the helical radiating element and<br />
extending along at least most <strong>of</strong> the first longitudinal portion.<br />
(21) 562237 (22) 5 Oct 2007 (23) 6 Oct 2008<br />
(54) Proliferation signature and prognosis for gastrointestinal cancer<br />
(51) IPC2011.01:C12Q1/68<br />
(71) PACIFIC EDGE BIOTECHNOLOGY LTD<br />
(72) Anjomshoaa, Ahmad; Reeve, Anthony Edmund; Lin, Yu-Hsin; Black,<br />
Michael A;<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) Provided is a method <strong>of</strong> predicting the likelihood <strong>of</strong> long-term survival<br />
<strong>of</strong> a gastrointestinal cancer patient without the recurrence <strong>of</strong><br />
gastrointestinal cancer, comprising determining the expression level <strong>of</strong><br />
one or more prognostic RNA transcripts or their expression products in a<br />
gastrointestinal sample obtained from the patient, normalized against<br />
the expression level <strong>of</strong> all RNA transcripts or their products in the<br />
gastrointestinal cancer tissue sample, or <strong>of</strong> a reference set <strong>of</strong> RNA transcripts<br />
or their expression products; wherein the prognostic RNA transcript<br />
or expression product comprises the transcript <strong>of</strong> replication factor<br />
(activator 1) 4 (RFC4); and establishing likelihood <strong>of</strong> long-term survival<br />
without gastrointestinal cancer recurrence wherein increased expression<br />
<strong>of</strong> the one or more prognostic RNA transcripts or their expression products<br />
indicates an increased likelihood <strong>of</strong> long-term survival without<br />
gastrointestinal cancer recurrence.<br />
Divisional filed as 584603<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 76 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(21) 562254 (22) 8 Mar 2006<br />
(54) Exterior sheathing weather barrier construction and method <strong>of</strong> manufacture<br />
(86) PCT/IB2006/002341 (87) WO2007/004066<br />
(51) IPC2011.01:E04C2/04; B28B19/00<br />
(71) BPB Limited<br />
(72) Hauber, Robert J; Hennis, Mark E; Fahey, Michael P; Boydston, Gerald<br />
D;<br />
(31) 05 78518 (32) 11 Mar 2005 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) A gypsum board panel comprises two facing main surfaces, at least<br />
one machine edge surface 295 with three dimensional features, at least<br />
one bull edge surface, and an outer gypsum layer 295 to which a polymer<br />
additive has been added. An adhesive material 385 which can form<br />
chemical cross-linking, co-polymer bonds with said polymer additive with<br />
the polymer additive in the outer gypsum layer is disposed on the machine<br />
edge surface.<br />
(21) 562363 (22) 18 Apr 2006<br />
(54) Process for the production <strong>of</strong> animal feed and ethanol and novel animal<br />
feed<br />
(86) PCT/US2006/014505 (87) WO2006/113683<br />
(51) IPC2011.01:A23K1/00; A23K3/00; B02B5/00; C12P7/06,08<br />
(71) ARCHER-DANIELS-MIDLAND COMPANY<br />
(72) Abbas, Charles; Binder, Thomas P; Beery, Kyle E; Cecava, Michael<br />
J; Holzgraefe, David P; Solheim, Leif P; Doane, Perry H;<br />
(31) 05 672779 (32) 19 Apr 2005 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed herein is a method for the production <strong>of</strong> ethanol and a<br />
modified animal feed. The method replaces the starch in known cornbased<br />
animal feed with biomass fiber treated to make it more digestible<br />
by animals. The process involves removing the pericarp from corn kernels<br />
to obtain a pericarp enriched fraction; contacting at least one <strong>of</strong> the<br />
pericarp enriched fraction and a lignocellulosic by-product <strong>of</strong> agricultural<br />
processing with a fiber hydrolyzing agent to at least partially hydrolyze<br />
lignocellulosic fibres and obtain a treated fiber fraction; removing the<br />
germ from said corn kernels, resulting in a starch and a protein; separating<br />
said protein from said starch; liquefying and saccharifying and fermenting<br />
said starch to produce a fermented starch broth; recovering<br />
ethanol and distillers dried grains from the fermented starch broth; and<br />
combining the treated fiber fraction with the distillers dried grains to form<br />
a modified distiller’s dried grain product. The modified animal feed may<br />
optionally include energy materials such as animal and vegetable fats,<br />
vegetable soapstocks, or glycerin, and combinations there<strong>of</strong>.<br />
(21) 562409 (22) 10 May 2006<br />
(54) Use <strong>of</strong> barusiban in assisted reproduction<br />
(86) PCT/PL2006/000029 (87) WO2006/121362<br />
(51) IPC2011.01:A61K31/404,4025,4439,452,4545,4709,495,501,5513;<br />
A61K38/12; A61K45/06; A61P15/06<br />
(71) Ferring International Center SA.<br />
(72) Kuczynski, Waldemar; Pierzynski, Piotr;<br />
(31) 05 374954 (32) 10 May 2005 (33) PL<br />
(31) 05 376607 (32) 12 Aug 2005 (33) PL<br />
(31) 05 733916 (32) 4 Nov 2005 (33) US<br />
(74) JAMES & WELLS, Level 12, KPMG Centre, 85 Alexandra Street,<br />
Hamilton, New Zealand<br />
(57) Disclosed is the use <strong>of</strong> barusiban for the manufacture <strong>of</strong> a medicament<br />
for an improved uterine receptivity in assisted reproduction.<br />
(21) 562456 (22) 31 May 2006<br />
(54) Method <strong>of</strong> producing haploid and doubled haploid plant embryos<br />
(86) PCT/EP2006/005238 (87) WO2006/128707<br />
(51) IPC2011.01:A01H1/02; A01H5/00; A01H1/08; A01H5/10<br />
(71) Rijk Zwaan Zaadteelt en Zaadhandel B.V.<br />
(72) Dirks, Robert Helene Ghislain; Angenent, Gerrit Cornelis; Lelivelt,<br />
Cecilia Lucia Clara; Custers, Johannes Bernardus Maria;<br />
(31) 05 05076264 (32) 31 May 2005 (33) EP<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) Provided is a method for producing haploid plant embryos, comprising<br />
the steps <strong>of</strong>: a) providing microspores or pollen that are transformed<br />
with a nucleic acid to comprise cell division inducing molecules; b) pollinating<br />
an embryo sac cell, <strong>of</strong> the plant <strong>of</strong> which the haploid embryo is to<br />
be made with the transformed microspores or pollen; c) allowing the transformed<br />
microspores or pollen to discharge the cell division inducing molecules<br />
in or in the vicinity <strong>of</strong> the embryo sac cell, to trigger division there<strong>of</strong><br />
to obtain a haploid plant embryo. Doubled haploid plants can also be<br />
produced by a similar method.<br />
(21) 562535 (22) 15 Mar 2006<br />
(54) Thermal conduction during alkaline extraction<br />
(86) PCT/EP2006/002344 (87) WO2006/108481<br />
(51) IPC2011.01:C13D1/08; A23F3/18; A23F5/26; C13D1/02<br />
(71) Sudzucker Aktiengesellschaft Mannheim/Ochsenfurt<br />
(72) Arnold, Jochen; Frenzel, Stefan; Michelberger, Thomas;<br />
(31) 05 05017446 (32) 15 Apr 2005 (33) DE<br />
(74) PHILLIPS ORMONDE FITZPATRICK, 367 Collins Street, Melbourne,<br />
Victoria 3000, Australia<br />
(57) Disclosed is a process for extracting biological material, selected from<br />
sugar beet, chicory and sugar can from sugar beet cossettes or sugar<br />
beets in an extraction system, wherein the temperature <strong>of</strong> the biological<br />
material in the extraction system is increased throughout the course <strong>of</strong><br />
the extraction from material feed to material discharge.<br />
(21) 562592 (22) 27 Apr 2006<br />
(54) Long-chain quaternary ammonium compounds as wood treatment<br />
agents<br />
(86) PCT/US2006/016134 (87) WO2006/118980<br />
(51) IPC2011.01:B27K3/15; B32B21/04; B32B23/04,06<br />
(71) Viance, LLC<br />
(72) Jin, Lehong; Preston, Alan F; Archer, Kevin J; Cui, Futong; Zahora,<br />
Andrew R; Walcheski, Paul J;<br />
(31) 05 121632 (32) 4 May 2005 (33) US<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) Disclosed is a composition comprising a wood preservative agent<br />
and a long-chain quaternary ammonium compound <strong>of</strong> formula (I), wherein<br />
R3 and R4 <strong>of</strong> the compound <strong>of</strong> formula (I) are long chain alkyl moieties<br />
having from 16-50 carbon atoms, unsubstituted or substituted with one<br />
or more N, O, S, or a halogen atoms. Also disclosed is a method <strong>of</strong><br />
treating wood, comprising impregnating wood with the said composition.<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 77 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(21) 562595 (22) 27 Apr 2006<br />
(54) Substituted amide derivatives as protein kinase inhibitors<br />
(86) PCT/US2006/016344 (87) WO2006/116713<br />
(51) IPC2011.01:C07D401/14; A61K31/435,495; A61P35/00; C07D401/<br />
12; C07D403/12; C07D405/14; C07D409/14; C07D413/12,14; C07D417/<br />
14; C07D487/04; C07D495/04<br />
(71) AMGEN INC.<br />
(72) Kim, Tae-Seong; Bauer, David; Bellon, Steven; Boezio, Alessandro;<br />
Booker, Shon; Choquette, Deborah; D’Amico, Derin C; D’Angelo, Noel;<br />
Dominguez, Celia; Fellows, Ingrid M; Germain, Julie; Graceffa, Russell;<br />
Harmange, Jean-Christophe; Hirai, Satoko; La, Daniel; Lee, Matthew;<br />
Norman, Mark H; Potashman, Michele; Roveto, Philip; Siegmund, Aaron<br />
C; Xi, Ning; Yang, Kevin; Liu, Longbin;<br />
(31) 05 675805 (32) 27 Apr 2005 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed are substituted amide derivatives as protein kinase inhibitors<br />
and which are effective for prophylaxis and treatment <strong>of</strong> diseases,<br />
such as HGF mediated diseases. The disclosure encompasses compounds,<br />
analogs, enantiomer, diastereomer, solvate, N-oxide there<strong>of</strong> and<br />
pharmaceutically acceptable salts there<strong>of</strong>, pharmaceutical compositions<br />
and methods for prophylaxis and treatment <strong>of</strong> diseases and other maladies<br />
or conditions involving, cancer and the like. The disclosure also<br />
relates to processes for making such compounds as well as to intermediates<br />
useful in such processes. These compounds may be represented<br />
by formula (II), wherein the variables are as defined in the specification.<br />
(21) 562623 (22) 28 Apr 2006<br />
(54) Method to transform bulk material<br />
(86) PCT/US2006/016319 (87) WO2006/119044<br />
(51) IPC2011.01:B02C19/00<br />
(71) GTL Energy Ltd.<br />
(72) French, Robert R; Reeves, Robert A;<br />
(31) 05 676621 (32) 29 Apr 2005 (33) US<br />
(74) JAMES & WELLS, Level 12, KPMG Centre, 85 Alexandra Street,<br />
Hamilton, New Zealand<br />
(57) Disclosed is a method <strong>of</strong> removing void spaces and vapors present in<br />
carbonaceous materials including the steps <strong>of</strong>:<br />
Comminuting a carbonaceous material to form a crushed material <strong>of</strong> reduced<br />
particle size;<br />
Compacting the crushed material in a counter-rotating roll compaction<br />
machine produce a compact; Separating vapors from the compact to<br />
form a dried carbonaceous product.<br />
Divisional filed as 590973<br />
(21) 562777 (22) 3 May 2006<br />
(54) A float with a damping means and keel<br />
(86) PCT/IE2006/000044 (87) WO2006/117767<br />
(51) IPC2011.01:A01K61/00; B63B22/16,18<br />
(71) Rodicon Limited; John Francis Concannon<br />
(72) Concannon, John Francis;<br />
(31) 05 0273 (32) 4 May 2005 (33) IE<br />
(31) 06 0215 (32) 20 Mar 2006 (33) IE<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) A float 1 comprises a hollow shell 5 having a front end 19 and a rear<br />
end 20, the hollow shell defining an airtight hollow interior region and a<br />
first major horizontal plane 8 that in use extends through the hollow shell<br />
5 at its maximum horizontal cross-sectional area, a damping projection<br />
12 extending completely around and laterally outwardly from the hollow<br />
shell 5 that dampens the buoyant movement <strong>of</strong> the hollow shell 5 in<br />
water in a generally vertical direction with the damping projection 12<br />
defining a second plane 14 parallel to the first major plane 8 defined by<br />
the hollow shell, and a keel 18 extending downwardly from the hollow<br />
shell 5 that minimises the rolling movement <strong>of</strong> the hollow shell 5. The<br />
keel 18 extends along the hollow shell 5 and terminates at the damping<br />
projection 12 adjacent to the front and rear ends <strong>of</strong> the hollow shell 5,<br />
and defines a corresponding keel plane 9 that extends perpendicularly<br />
to the second horizontal plane 14 defined by the damping projection 12.<br />
Divisional filed as 590877<br />
(21) 562967 (22) 9 May 2006<br />
(54) Breath actuated drug delivery system with nasal delivery<br />
(86) PCT/US2006/018252 (87) WO2007/001650<br />
(51) IPC2011.01:A61M15/00<br />
(71) KOS LIFE SCIENCES, INC.<br />
(72) Williams, Robert; Ruckdeschel, Thomas; Khare, Matthew; Deaton,<br />
Daniel;<br />
(31) 05 160493 (32) 27 Jun 2005 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) A nasal drug delivery system comprises a container 110 containing a<br />
substance to be delivered into the nasal passages <strong>of</strong> a user, a nasal<br />
shaft 108 extending from the drug delivery system for placement in or<br />
around the nose <strong>of</strong> user and in fluid communication with a valve <strong>of</strong> the<br />
container, the valve comprising a vertical lumen 132 and an angled lumen<br />
134, an oral shaft 106 extending from the drug delivery system for<br />
placement in the mouth <strong>of</strong> a user, and a pressure activated diaphragm<br />
120 trigger means. Upon application <strong>of</strong> pressure to the oral shaft the<br />
diaphragm trigger means releases a predetermined amount <strong>of</strong> the substance<br />
from the container 110 to the nasal shaft 108. The pressure activated<br />
diaphragm trigger means comprises a follower assembly 114, a<br />
follower 116, and a cam 118.<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 78 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(21) 562968 (22) 7 Apr 2006<br />
(54) Breath actuated nasal drug delivery system<br />
(86) PCT/US2006/012949 (87) WO2007/001585<br />
(51) IPC2011.01:A61M15/00<br />
(71) KOS LIFE SCIENCES, INC.<br />
(72) Williams, Robert; Ruckdeschel, Thomas; Khare, Matthew; Deaton,<br />
Daniel;<br />
(31) 05 160493 (32) 27 Jun 2005 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) A nasal drug delivery system comprises a container containing a substance<br />
to be delivered into the nasal passages <strong>of</strong> a user, a nasal shaft<br />
extending from the drug delivery system for placement in or around the<br />
nose <strong>of</strong> user and in fluid communication with a valve <strong>of</strong> the container, the<br />
valve comprising a vertical lumen 132 and an angled lumen 134, an oral<br />
shaft extending from the drug delivery system for placement in the mouth<br />
<strong>of</strong> a user, and a pressure activated diaphragm trigger means. Upon application<br />
<strong>of</strong> pressure to the oral shaft the diaphragm trigger means releases<br />
a predetermined amount <strong>of</strong> the substance from the container to<br />
the nasal shaft .<br />
(21) 562969 (22) 13 Jun 2006<br />
(54) Modifiers for gypsum slurries and method <strong>of</strong> using them<br />
(86) PCT/US2006/022936 (87) WO2006/138277<br />
(51) IPC2011.01:C04B28/14; B32B1/04; C04B11/00<br />
(71) UNITED STATES GYPSUM COMPANY<br />
(72) Lettkeman, Dennis M; Shake, Michael P; Liu, Qingxia; Wilson, John<br />
W; Randall, Brian; Blackburn, David R;<br />
(31) 05 152317 (32) 14 Jun 2005 (33) US<br />
(31) 06 450068 (32) 9 Jun 2006 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed herein is a gypsum slurry that includes water, calcium sulphate<br />
hemihydrate, a polycarboxylate dispersant and a modifier which is<br />
a phosphonate. The modifier is chemically configured to improve the<br />
efficacy <strong>of</strong> the polycarboxylate dispersant.<br />
(21) 563047 (22) 5 Apr 2006<br />
(54) Modal interval processor<br />
(86) PCT/US2006/012547 (87) WO2006/107996<br />
(51) IPC2011.01:G06F7/38<br />
(71) Sunfish Studio, Inc.<br />
(72) Hayes, Nathan T;<br />
(31) 05 668539 (32) 5 Apr 2005(33) US<br />
(31) 05 722107 (32) 30 Sep 2005 (33) US<br />
(31) 05 722103 (32) 30 Sep 2005 (33) US<br />
(31) 05 723216 (32) 3 Oct 2005 (33) US<br />
(31) 05 723059 (32) 3 Oct 2005 (33) US<br />
(31) 05 723249 (32) 3 Oct 2005 (33) US<br />
(74) Pizzeys <strong>Patent</strong> and Trade Mark Attorneys, Level 2, Woden Plaza<br />
<strong>Office</strong>s, Woden Town Square, Woden, ACT 2606, Australia<br />
(57) A logic circuit for computing first and second modal interval (MI) result<br />
values is disclosed. The values are <strong>of</strong> at least first and second different<br />
MI functions responsive to respectively, first and second values <strong>of</strong> a selector<br />
signal. The computing is based on at least one MI operand value<br />
encoded in an operand signal. Each MI value comprises first and second<br />
multi-bit set theoretical numbers (STN) and the STNs define first and<br />
second end points <strong>of</strong> a range <strong>of</strong> real numbers. The logic circuit further<br />
encodes one <strong>of</strong> the universal and existential quantification values.<br />
The logic circuit includes at least first and second arithmetic functional<br />
units (AFUs) each connected to receive the operand signal. The AFUs<br />
perform an arithmetic operation using as the arguments therefor, each<br />
MI operand value encoded in the operand signal, and respectively provide<br />
the first and second MI result values in first and second result signals.<br />
The logic circuit also includes a multiplexer having a selector input<br />
receiving the selector signal having a multibit output port for providing an<br />
output signal encoding a MI result value, and having at least first and<br />
second multi-bit input ports. The first and second input ports are connected<br />
to receive respectively the first and second result signals provided<br />
as the operand signals by the first and second AFUs, and each<br />
input port is associated with a single selector signal value. The multiplexer<br />
supplies, encoded in an output signal provided by the output port,<br />
the MI result value provided at the input port there<strong>of</strong> associated with the<br />
current selector signal value. The logic circuit also includes a result register<br />
for storing each MI result value, connected to receive the values<br />
respectively provided by the multiplexer output port.<br />
Divisional filed as 579183<br />
(21) 563073 (22) 2 May 2006<br />
(54) Interactive large scale touch surface system<br />
(86) PCT/CA2006/000706 (87) WO2006/116869<br />
(51) IPC2011.01:G06F3/01,041,042,048<br />
(71) SMART TECHNOLOGIES INC<br />
(72) Hill, Douglas; Beckie, Niel; Van Ieperen, Taco; Vdovine, Serguei;<br />
Sirotich, Roberto; Fletcher, Mark; Tallman, Scott; Williams, Marilyn; Bill,<br />
Shane Edward; Goodman, Shannon Patricia;<br />
(31) 05 118626 (32) 2 May 2005 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) A method <strong>of</strong> facilitating user interaction with an image displayed on a<br />
touch surface <strong>of</strong> a large scale touch system is disclosed.<br />
Images <strong>of</strong> the touch surface are captured with sets <strong>of</strong> camera devices<br />
positioned in series along the length <strong>of</strong> the touch surface. Each set <strong>of</strong><br />
camera devices comprises at least two laterally spaced camera devices<br />
having overlapping fields <strong>of</strong> view oriented to look generally across the<br />
touch surface. The captured images are processed to detect user interaction<br />
with the touch surface.<br />
A scaled version <strong>of</strong> at least a portion <strong>of</strong> the displayed image is displayed<br />
on the touch surface at a user accessible location in response to an<br />
associated input gesture made at an arbitrary location on the touch surface.<br />
The scaled version is displayed adjacent the location <strong>of</strong> the input<br />
gesture. Coordinates <strong>of</strong> the displayed scaled version to the corresponding<br />
coordinate portion <strong>of</strong> the displayed image are mapped so that user<br />
interactions with the displayed scaled version are translated to interactions<br />
with the displayed image.<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 79 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
A writing input region can be further displayed on the touch surface adjacent<br />
a user accessible location in response to an associated input gesture<br />
made at an arbitrary location on the touch surface.<br />
The writing input into the writing input region via pointer interaction with<br />
the touch surface is detected and the detected writing input is displayed<br />
as text in a text display region on the touch surface at a location spaced<br />
from the writing input region. The position <strong>of</strong> at least one <strong>of</strong> the writing<br />
input region and the text display region on the touch surface is changed<br />
in response to user interaction with the touch surface.<br />
At least one portion <strong>of</strong> the displayed image can be reproduced on the<br />
touch surface at a user accessible location in response to an associated<br />
input gesture made at an arbitrary location on the touch surface and<br />
coordinates <strong>of</strong> the reproduced portion to the corresponding coordinate<br />
portion <strong>of</strong> the displayed image are mapped so that user interactions with<br />
the reproduced portion are translated to interactions with the corresponding<br />
portion <strong>of</strong> the displayed image.<br />
(21) 563119 (22) 4 Apr 2006<br />
(54) Self expanding flexible stent comprising a helical strut member and<br />
multiple helical elements<br />
(86) PCT/US2006/012579 (87) WO2006/108010<br />
(51) IPC2011.01:A61F2/06,90,82<br />
(71) Flexible Stenting Solutions, Inc.<br />
(72) Burpee, Janet; Beach, Bradley;<br />
(31) 05 667613 (32) 4 Apr 2005(33) US<br />
(31) 05 250226 (32) 14 Oct 2005 (33) US<br />
(31) 04 397987 (32) 4 Apr 2006(33) US<br />
(74) FISHER ADAMS KELLY, Level 29, 12 Creek Street, Brisbane, Queensland<br />
4000, Australia<br />
(57) A self expanding flexible stent 10 comprises a helical strut member<br />
12 helically wound about an axis <strong>of</strong> the stent 10, the helical strut member<br />
12 comprising several helical strut elements 12, and several helical<br />
elements 16 helically wound about the axis <strong>of</strong> the stent 10 in the same<br />
direction <strong>of</strong> the helical strut member 12 with the helical elements 16<br />
extending between and interconnecting points on subsequent windings<br />
<strong>of</strong> the helical strut member 12 , where the helical elements 16 are elongated<br />
elements 16 both in the compressed state and deployed state.<br />
The distance between at least some adjacent helical elements 16 in the<br />
compressed state varies along the length <strong>of</strong> the adjacent helical elements<br />
16 and is in a range from zero and about the maximum distance<br />
between adjacent helical elements 16 in the deployed state. The stent<br />
10 in the compressed state is longer than in the deployed state, and in<br />
the deployed state the elongated elements 16 are substantially parallel<br />
and the helical strut member 12 and the helical strut elements 16 define<br />
a cylinder having a constant diameter.<br />
Divisional filed as 588872<br />
(21) 563123 (22) 2 May 2006<br />
(54) Acrylate and methacrylate-based sdhesive formulations for metal<br />
bonding applications<br />
(86) PCT/US2006/017290 (87) WO2006/119469<br />
(51) IPC2011.01:C09J4/00<br />
(71) Illinois Tool Works Inc.<br />
(72) Wang, Xiaobin; Doe, Daniel K; Savory, Patricia M; Lambert, Kenneth<br />
A;<br />
(31) 05 120789 (32) 3 May 2005 (33) US<br />
(74) PHILLIPS ORMONDE FITZPATRICK, 367 Collins Street, Melbourne,<br />
Victoria 3000, Australia<br />
(57) Disclosed is an adhesive formulation, including: an activator part comprising<br />
an initiator; and an adhesive part comprising:<br />
an acrylate monomer or a methacrylate monomer, or a combination<br />
there<strong>of</strong>;and a chelating agent solution wherein at least a portion <strong>of</strong> a<br />
solvent <strong>of</strong> the chelating solution is water, the chelating agent solution<br />
comprising at least 1 percent by weight <strong>of</strong> the adhesive part; and<br />
a combination <strong>of</strong> at least two toughening agents, wherein the combination<br />
comprises: at least one toughening agent having a glass transition<br />
temperature <strong>of</strong> at least one domain in the range <strong>of</strong> -25 Deg C to -50 Deg<br />
C (-13 Deg F to -58 Deg F); and at least one other toughening agent<br />
having a glass transition temperature <strong>of</strong> at least one domain lower than -<br />
50 Deg C (-58 Deg F).<br />
Divisional filed as 590178<br />
(21) 563202 (22) 13 Jul 2006<br />
(54) Thiophene compounds and thrombopoietin receptor activators<br />
(86) PCT/JP2006/314317 (87) WO2007/010954<br />
(51) IPC2011.01:C07D333/32; C07D409/12<br />
(71) Nissan Chemical Industries, Ltd.<br />
(72) Miyaji, Katsuaki; Yanagihara, Kazufumi; Shigeta, Yukihiro; Iwamoto,<br />
Shunsuke; Horikawa, Masato; Owada, Shingo; Nakano, Satoshi; Ota,<br />
Hir<strong>of</strong>umi; Ishiwata, Norihisa; Hirokawa, Yukata;<br />
(31) 05 206822 (32) 15 Jul 2005 (33) JP<br />
(31) 05 206823 (32) 15 Jul 2005 (33) JP<br />
(31) 06 083770 (32) 24 Mar 2006 (33) JP<br />
(31) 06 083771 (32) 24 Mar 2006 (33) JP<br />
(31) 06 115569 (32) 19 Apr 2006 (33) JP<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) A 3-hydroxythiophene-3-yl hydrazide represented by the formula (I):<br />
wherein R1 is a phenyl group. R2 is a hydrogen atom or an alkyl group,<br />
R3 is a phenyl group, a pyridyl group or a thienyl group and R4 is a<br />
hydrogen atom or an alkyl group, a tautomer, prodrug or pharmaceutically<br />
acceptable salt <strong>of</strong> the compound or a solvate there<strong>of</strong>. Also disclosed is<br />
the use <strong>of</strong> said hydrazide for increasing platelets.<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 80 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(21) 563252 (22) 14 Apr 2006<br />
(54) Containment pen comprising panels having mesh material between<br />
struts<br />
(86) PCT/US2006/014404 (87) WO2006/113619<br />
(51) IPC2011.01:A01K63/00<br />
(71) OCEAN FARM TECHNOLOGIES INC.<br />
(72) Cartwright, Paul; Page, Stephen H;<br />
(31) 05 671861 (32) 14 Apr 2005 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed is a finfish aquaculture containment pen (10) in a polyhedral<br />
structure. The pen comprises: a plurality <strong>of</strong> panels (12) that when<br />
joined together form the majority <strong>of</strong> the exterior surface <strong>of</strong> the containment<br />
pen; a plurality <strong>of</strong> compression-bearing struts extending along the<br />
boundaries between panels; and a plurality <strong>of</strong> hubs at which some <strong>of</strong> the<br />
struts and the comers <strong>of</strong> some <strong>of</strong> the panels abut each other. The panels<br />
each comprise tension-bearing mesh material forming the exterior surface<br />
<strong>of</strong> the containment pen, and the mesh material is attached to the<br />
struts along the lengths <strong>of</strong> the struts.<br />
(21) 563267 (22) 26 Apr 2006<br />
(54) Vacuum vessel for treatment <strong>of</strong> oils<br />
(86) PCT/SE2006/000502 (87) WO2006/118517<br />
(51) IPC2011.01:C11B3/14; B01D3/34; C11B3/16<br />
(71) ALFA LAVAL CORPORATE AB<br />
(72) Gullov-Rasmussen, Bjarne;<br />
(31) 05 0501008 (32) 29 Apr 2005 (33) SE<br />
(74) HENRY HUGHES, 119-125 Willis Street, Wellington, New Zealand<br />
(57) A vacuum vessel for continuous or semi-continuous treatment <strong>of</strong> oils<br />
in connection with deodorization comprises spaces 12 through which oil<br />
to be treated is brought to pass and means to heat or cool the oil in the<br />
form <strong>of</strong> U-tubes. There are perforated pipes 26 arranged at the bottom <strong>of</strong><br />
the spaces to lead stripping gas into the oil. The vessel has a connection<br />
to a vacuum source (7). The spaces in the vessel are arranged such that<br />
the oil to be treated in the vessel flows through the same by gravity. The<br />
heating or cooling medium passing the U-tubes is arranged to be pumped<br />
there through. The U-tubes for heating or cooling medium are arranged<br />
in such a way in the spaces that the flow <strong>of</strong> oil is counter-current to the<br />
flow <strong>of</strong> heating or cooling medium all through the vessel and a number <strong>of</strong><br />
U-tubes are arranged in groups, parallel and in rows above each other in<br />
the spaces.<br />
(21) 563315 (22) 2 May 2006<br />
(54) A device that can be used for bracing the pelvic region <strong>of</strong> a patient<br />
(86) PCT/AU2006/000573 (87) WO2006/116811<br />
(51) IPC2011.01:A61F5/01; A61G1/013,044<br />
(71) Martin Richardson<br />
(72) Richardson, Martin;<br />
(31) 05 902215 (32) 2 May 2005 (33) AU<br />
(74) JAMES & WELLS, Level 12, KPMG Centre, 85 Alexandra Street,<br />
Hamilton, New Zealand<br />
(57) A device that can be used for bracing the pelvic region <strong>of</strong> a patient is<br />
disclosed. The device includes a plurality <strong>of</strong> bracing elements. One or<br />
more <strong>of</strong> the bracing elements include first and second straps and an<br />
attachment means. The first strap is detachably connected to the second<br />
strap at a first point <strong>of</strong> interconnection. The interconnection can be<br />
moved along the second strap so that the combined length <strong>of</strong> the first<br />
and second straps can be altered. This alteration allows adjustment <strong>of</strong><br />
the length <strong>of</strong> the bracing element that can be wrapped at least in part<br />
around or about the pelvic region <strong>of</strong> a patient. The attachment means, in<br />
use, can detachably interconnect the second strap directly or indirectly<br />
to the first strap so that the bracing element forms a closed loop that can<br />
at least partially be wrapped around or about the patient. The attachment<br />
means detachably interconnects the first and second straps at a second<br />
point <strong>of</strong> interconnection. The second interconnection can be moved along<br />
the first strap to further adjust the length <strong>of</strong> the bracing element can be<br />
wrapped at least in part around the pelvic region <strong>of</strong> a patient.<br />
(21) 563332 (22) 22 May 2006<br />
(54) Wall assembly using corrugated panels snapped in place to a supporting<br />
rail on the floor or ceiling by a plug<br />
(86) PCT/AU2006/000674 (87) WO2006/122375<br />
(51) IPC2011.01:E04B1/66; E04B2/72; E04F19/00<br />
(71) Steel Storage Holdings Pty Ltd<br />
(72) Perrin, Jonathon Gilbert Francis; Ryan, Gerard Michael;<br />
(31) 05 902629 (32) 20 May 2005 (33) AU<br />
(74) WYNNES - PATENT AND TRADE MARK ATTORNEYS, Level 3,<br />
Waterfront Place, 1 Eagle Street, Brisbane, QLD 4121, Australia<br />
(57) A securing cap (43) used in the wall (40) <strong>of</strong> a building is disclosed.<br />
The cap (43) fills the gap in a single space formed between two adjacent<br />
corrugations (44) in the wall (40) and a floor or ceiling mounting (42). The<br />
cap (43) has a cover portion and one or more legs extending downwardly<br />
from the cover portion. The cap also has one or more protrusions to<br />
engage with the corrugated wall (40) and the floor or ceiling mounting<br />
(42). The protrusions snap fit into openings in the wall (40) and engage a<br />
lip on the floor or ceiling mounting (42) to enclose the single space and<br />
facilitate fixing <strong>of</strong> the wall (40) to the floor or ceiling mounting (42).<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 81 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(21) 563361 (22) 31 May 2006<br />
(54) HCV protease inhibitors in combination with food<br />
(86) PCT/US2006/021115 (87) WO2006/130686<br />
(51) IPC2011.01:C07K5/08; A61K31/40; A61P31/12<br />
(71) Schering Corporation<br />
(72) Zhang, Jenny; Gupta, Samir K;<br />
(31) 05 686925 (32) 2 Jun 2005 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed herein is the use <strong>of</strong> compounds which are useful for treating<br />
a wide variety <strong>of</strong> diseases or disorders associated with hepatitis C<br />
virus ("HCV") by inhibiting HCV protease (ie HCV NS3/NS41 serine protease).<br />
The compounds are administered concurrently with the consumption<br />
<strong>of</strong> food, or up to 90 minutes after the consumption <strong>of</strong> food, or<br />
up to 30 minutes before the consumption <strong>of</strong> food to enhance absorption<br />
<strong>of</strong> the compounds in the gastrointestinal tract and increase the<br />
bioavailability <strong>of</strong> the compounds.<br />
(21) 563365 (22) 31 May 2006<br />
(54) Combination <strong>of</strong> HCV protease inhibitors with a surfactant<br />
(86) PCT/US2006/021003 (87) WO2006/130628<br />
(51) IPC2011.01:A61K31/454; A61K38/05,06; A61P31/14<br />
(71) Schering Corporation<br />
(72) Malcolm, Bruce A; Bradley, Prudence K; Pavlovsky, Anastasia; Cho,<br />
Wing-Kee Philip; Qiu, Zhihui;<br />
(31) 05 686945 (32) 2 Jun 2005 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed is a formulation for treating HCV infection comprising sodium<br />
lauryl sulphate and a compound <strong>of</strong> formula Ia, 1b, or IC. The said<br />
formulation is in the form <strong>of</strong> a capsule, a tablet, a gel, a suppository, a<br />
powder or a fluid. The use <strong>of</strong> the said formulation for the manufacture <strong>of</strong><br />
a medicament for the treatment <strong>of</strong> HCV infection is also disclosed.<br />
(21) 563416 (22) 18 May 2006<br />
(54) Electrostatic separation <strong>of</strong> mineral products with foreign particles being<br />
triboelectrically charged<br />
(86) PCT/EP2006/062425 (87) WO2006/122967<br />
(51) IPC2011.01:B03C7/00; B02C23/08; B03C3/15<br />
(71) OMYA G<strong>MB</strong>H<br />
(72) Mangelberger, Thomas; Tavakkoli, Bahman;<br />
(31) 05 05023950 (32) 20 May 2005 (33) DE<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) A method for manufacturing dispersed mineral products by grinding<br />
the mineral raw material, sizing the same in a flow classifier, sorting the<br />
same in dispersion in air, and eliminating the dispersion air. The method<br />
includes triboelectrically charging the dispersed mineral particles <strong>of</strong> the<br />
particle-air dispersion during the sizing process and directing the charged<br />
particles through an electrostatic separation chamber in order to separate<br />
the foreign particles from the valuable particles.<br />
(21) 563446 (22) 2 Jun 2006<br />
(54) Combination <strong>of</strong> pyrimidylaminobenzamide compounds and imatinib<br />
for treating or preventing proliferative diseases<br />
(86) PCT/US2006/021307 (87) WO2006/132930<br />
(51) IPC2011.01:A61K31/506; A61P35/00<br />
(71) Novartis AG<br />
(72) Alland, Leila; Manley, Paul W; Mestan, Juergen;<br />
(31) 05 687758 (32) 3 Jun 2005 (33) US<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 82 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) Disclosed is the use <strong>of</strong> a combination <strong>of</strong> 4-Methyl-3-[[4-(3-pyridinyl)-<br />
2-pyrimidinyl]amino]-N-[5-(4-methyl-1H-imidazol-1-yl)-3-<br />
(trifluoromethyl)phenyl] benzamide, or a pharmaceutically acceptable salts<br />
there<strong>of</strong>, <strong>of</strong> the formula (II); and imatinib for the formula (III) or<br />
pharmaceutically acceptable salts there<strong>of</strong>, for the preparation <strong>of</strong> a medicament<br />
for the treatment <strong>of</strong> gastrointestinal stromal tumours.<br />
(21) 563455 (22) 16 May 2006<br />
(54) Post-transcriptional regulation <strong>of</strong> gene expression in plants using a<br />
destablising sequence selected from a 3’SAUR terminator, a DST element,<br />
an ATTTA motif, an ATTTAA motif or a combination <strong>of</strong> ATTTA and<br />
ATTTAA motifs<br />
(86) PCT/US2006/018736 (87) WO2006/124777<br />
(51) IPC2011.01:C12N15/82<br />
(71) MONSANTO TECHNOLOGY LLC<br />
(72) Thai, Kwan Y; Wang, Qi; Dabrowski, John P; Ulmasov, Tim N; House,<br />
Ida M;<br />
(31) 05 682471 (32) 19 May 2005 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed is a method to post-transcriptionally decrease message<br />
stability <strong>of</strong> an exogenous gene <strong>of</strong> interest in a seed <strong>of</strong> a crop plant. The<br />
method comprises expressing said exogenous gene in a seed tissue,<br />
wherein said gene comprises a destabilising sequence in the 3’<br />
untranslated region, whereby message stability <strong>of</strong> said gene <strong>of</strong> interest<br />
is post-transcriptionally decreased in the seed. The destabilising sequence<br />
<strong>of</strong> the disclosed method comprises a 3’SAUR terminator, a DST element,<br />
an ATTTA motif, an ATTTAA motif or a combination <strong>of</strong> ATTTA and<br />
ATTTAA motifs.<br />
(21) 563508 (22) 18 Oct 2007<br />
(54) A panel with interlocking members<br />
(86) PCT/AU2007/001590 (87) WO2008/046154<br />
(51) IPC2011.01:E06B9/01; E04F11/18; E06B7/082; E04C2/42; E04H17/<br />
14<br />
(71) ALAN BROWNBILL; Danielle Tiffany Brownbill<br />
(72) Brownbill, Alan;<br />
(31) 06 230672 (32) 18 Oct 2006 (33) AU<br />
(74) CULLEN & CO, Level 32, 239 George Street, Brisbane, QLD 4001,<br />
Australia<br />
(57) Disclosed is a panel including a) a plurality <strong>of</strong> first members (11)<br />
disposed in a first direction, b) at least one second member (12) disposed<br />
in a second direction provided with i) a longitudinal opening extending<br />
at least partially through the at least one second member; ii) a<br />
one or more lateral openings intersecting the longitudinal opening to re-<br />
ceive at least a portion <strong>of</strong> respective first members, and iii) at least one<br />
locking member provided adjacent each lateral opening to abut a first<br />
member forced into the lateral opening, to lock the first member relative<br />
to the second member through application <strong>of</strong> compressive force to the<br />
first member.<br />
(21) 563564 (22) 31 May 2006<br />
(54) Phosphatidylserine enriched milk fractons for the formulation <strong>of</strong> functional<br />
foods<br />
(86) PCT/DK2006/000303 (87) WO2006/128465<br />
(51) IPC2011.01:A23L2/00; A23C9/00; A23G1/00; A23J7/00; A23L1/29<br />
(71) ARLA FOODS A<strong>MB</strong>A<br />
(72) Burling, Hans; Andersson, Ingemar; Schneider, Michael;<br />
(31) 05 685527 (32) 31 May 2005 (33) US<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) Provided is a process for the preparation <strong>of</strong> a phosphatidylserine (PS)<br />
source derived from bovine milk, containing at least 0.2%<br />
phosphatidylserine calculated on the weight <strong>of</strong> total lipids, by performing<br />
the steps <strong>of</strong>: centrifuging cream for butter oil production to a cream containing<br />
about 80 % <strong>of</strong> fat; breaking the resulting emulsion by high shearing<br />
to obtain a butter milk together with a butter oil; collecting the butter<br />
milk; separating fat from the butter milk to give butter milk containing<br />
about 70-80% phospholipids in the total lipids in the butter milk; treating<br />
the fat-separated butter milk by ultrafiltration to provide a concentrate;<br />
and spray-drying the resulting concentrate. Further provided are products<br />
produced by the process.<br />
Divisional filed as 582411<br />
(21) 563606 (22) 21 Nov 2007 (23) 21 Nov 2008<br />
(54) An expanded food product comprising hominy<br />
(51) IPC2011.01:A23L1/10<br />
(71) CORSON GRAIN LIMITED<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 83 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(72) Hardacre, Allan Keith;<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) Provided is an expanded food product comprising about 49-94.3% w/<br />
w hominy and about 5-60% w/w dairy protein isolate(s). The dairy protein<br />
isolates can be selected from lactic casein, MPC 85, MPC70, WPC392,<br />
WP1894, Alatel 825 or a mixture there<strong>of</strong> and can be included in breakfast<br />
cereals and snack food.<br />
(21) 563644 (22) 28 Apr 2006<br />
(54) A system with a shielded electrical cable with an armour that is exposed<br />
when entering an apparatus<br />
(86) PCT/GB2006/001549 (87) WO2006/114636<br />
(51) IPC2011.01:H04B3/56; H02G15/00,10<br />
(71) Manx Electricity Authority<br />
(72) Mcghee, Stephen; Jones, Alfred; Patrick, Matthew William;<br />
(31) 05 0508673 (32) 28 Apr 2005 (33) GB<br />
(74) PHILLIPS ORMONDE FITZPATRICK, 367 Collins Street, Melbourne,<br />
Victoria 3000, Australia<br />
(57) Disclosed is an electrical system for data transmission over an electricity<br />
distribution network. The system comprises <strong>of</strong> an electrical apparatus<br />
and a shielded electrical cable (3) connected to the apparatus, the<br />
cable having a core, a metallic sheath (35) around the core and surrounding<br />
armour (36). The armour is disengaged from around the metallic<br />
sheath at a location where the sheath enters the apparatus and is<br />
connected to and supported relative to the apparatus by means <strong>of</strong> a<br />
coupling such that a portion <strong>of</strong> the sheath is exposed between the location<br />
and the armour. The coupling comprises a first end arranged to receive<br />
the armour and a second end spaced from, but connected to, the<br />
first end, which second end being mounted to a part <strong>of</strong> the apparatus.<br />
Divisional filed as 588685<br />
(21) 563658 (22) 26 Apr 2006<br />
(54) Treatment station for a water drainage conduit with sediment collection<br />
(86) PCT/GB2006/001522 (87) WO2006/114621<br />
(51) IPC2011.01:E03F1/00; E03F5/14,16<br />
(71) THE UNIVERSITY COURT OF THE UNIVERSITY OF EDINBURGH;<br />
Iain Alexander Stewart Robinson<br />
(72) Cunningham, Colin John; Robinson, Iain Alexander Stewart;<br />
(31) 05 0508483 (32) 27 Apr 2005 (33) GB<br />
(74) HENRY HUGHES, 119-125 Willis Street, Wellington, New Zealand<br />
(57) Disclosed is a treatment station for a water drainage conduit (8). The<br />
station comprises; a chamber (1) having inlet (10) and outlet (6) means<br />
in fluid communication with upstream and downstream sections <strong>of</strong> the<br />
conduit and a sediment collection portion (14). Water enters the chamber<br />
via the inlet means collecting in the sediment collection portion until<br />
it reaches a level in the chamber such that it flows out <strong>of</strong> the outlet means.<br />
The chamber is provided with a filter means mount for releasably mount-<br />
ing a filter means (22) above the sediment collection portion for the upwards<br />
flowing filtration <strong>of</strong> water passing through the chamber to remove<br />
organic contaminants. The treatment station is further provided with access<br />
means (46) for removal and replacement <strong>of</strong> said filter means and<br />
the removal <strong>of</strong> solid material deposited in the sediment collection portion.<br />
The treatment station further comprises a preliminary sediment collection<br />
chamber (40), upstream <strong>of</strong> the chamber with the sediment collection<br />
portion and filter means mount.<br />
(21) 563785 (22) 3 May 2006<br />
(54) Mutation in OAS1 genes<br />
(86) PCT/US2006/016983 (87) WO2006/119363<br />
(51) IPC2011.01:C12N9/12; A61K38/16; C12Q1/68<br />
(71) Illumigen Biosciences, Inc.<br />
(72) Iadonato, Shawn P; Magness, Charles L; Scherer, Christina A; Fellin,<br />
P, Campion; Hagen, Tory; Olson, Amy;<br />
(31) 05 677680 (32) 4 May 2005 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Provided is an oligoadenylate synthetase 1 protein comprising a<br />
polypeptide having a specified amino acid sequence with at least one<br />
amino acid modification at position 1, 24, 25, 28, 31, 36, 47, 53, 54, 64,<br />
69, 74, 104, 108, 112, 113, 114, 115, 116, 117, 118, 119, 127, 130, 139,<br />
142, 160, 161, 162, 166, 175, 179, 226, 242, 246, 248, 250, 254, 274,<br />
279, 282, 284, 288, 289, 292, 295, 314, 315 and 335. Further provided<br />
are corresponding antisense and RNAi molecules, ribozymes and antibodies.<br />
The compositions are useful in treating viral diseases.<br />
Divisional filed as 584132<br />
(21) 563787 (22) 9 May 2006<br />
(54) Apparatus and method for displaying vinyl records<br />
(86) PCT/GB2006/001705 (87) WO2006/120436<br />
(51) IPC2011.01:A47G1/06; A47F7/14; G11B33/04<br />
(71) MEMORY BOX UK LIMITED<br />
(72) Heeps, Andrew Nicholas;<br />
(31) 05 0509446 (32) 9 May 2005 (33) GB<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Display apparatus 2 comprises first and second parts pivotally mounted<br />
to each other, where the first part comprises a window 6 through which<br />
the item to be displayed can be viewed and the second part comprises<br />
means 36, 38, 40, 42 for mounting the display apparatus 2 to a wall. A<br />
catch that limits the relative rotation <strong>of</strong> the two parts is included in one<br />
part. One part further comprises means for pressing an item located<br />
between the two parts against the other part.<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 84 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(21) 563829 (22) 26 May 2006<br />
(54) Device, system, and method for epithelium protection during cornea<br />
reshaping<br />
(86) PCT/US2006/020563 (87) WO2006/128038<br />
(51) IPC2011.01:A61B18/18; A61F9/007,008,009,01,013<br />
(71) NTK Enterprises, Inc.<br />
(72) Berry, Michael J; Woodward, Benjamin W;<br />
(31) 05 684749 (32) 26 May 2005 (33) US<br />
(31) 05 695175 (32) 29 Jun 2005 (33) US<br />
(31) 06 440794 (32) 25 May 2006 (33) US<br />
(74) Freehills <strong>Patent</strong> & Trade Mark Attorneys, Level 43, 101 Collins Street,<br />
Melbourne, Victoria 3000, Australia<br />
(57) A system 100 comprises a light source 106 operable to generate light<br />
energy 218 for a cornea reshaping procedure, and a device 102 operable<br />
to be attached to an eye 104 having a cornea 204. The device 102<br />
includes a window 210 operable to contact at least a portion <strong>of</strong> the cornea<br />
204 and to substantially or completely flatten at least part <strong>of</strong> the<br />
contacted surface <strong>of</strong> the cornea. The window 210 is substantially transparent<br />
to the light energy 218 that irradiates the cornea 204 during the<br />
cornea reshaping procedure, and is also operable to cool at least a portion<br />
<strong>of</strong> a corneal epithelium in the cornea 204 during the cornea reshaping<br />
procedure<br />
(21) 563863 (22) 2 Jun 2006<br />
(54) Agent for regeneration and/or protection <strong>of</strong> nerves<br />
(86) PCT/JP2006/311084 (87) WO2006/129788<br />
(51) IPC2011.01:A61K45/00; A61K31/426,427; A61K47/40; A61P19/08;<br />
A61P25/00; A61P43/00; A61P9/00; C07D277/20,56; C07D417/12<br />
(71) ONO PHARMACEUTICAL CO., LTD.<br />
(72) Ohmoto, Kazuyuki; Kinoshita, Akihiro; Matsuya, Hidekazu;<br />
(31) 05 164458 (32) 3 Jun 2005 (33) JP<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) The disclosure relates to an compound <strong>of</strong> formula (I-3) which is an<br />
agent for regeneration and/or protection <strong>of</strong> nerves. More particularly, it<br />
relates to an agent for regeneration and/or protection <strong>of</strong> nerves comprising<br />
an EP2 agonist which may have an EP3 agonistic effect. The compound<br />
<strong>of</strong> formula (I-3) is therefore useful as a therapeutic agent for a<br />
disease <strong>of</strong> the peripheral nervous system, such as a lower or upper motor<br />
neuron disease, a nerve root disease, plexopathy, thoracic outlet compression<br />
syndrome, peripheral neuropathy, neur<strong>of</strong>ibromatosis and neu-<br />
romuscular transmission disease. An EP2 agonist which has an EP3<br />
agonistic effect is a safe and effective agent for the regeneration and/or<br />
protection <strong>of</strong> nerves which has little influence on the circulatory system.<br />
(21) 563867 (22) 8 May 2006<br />
(54) Non-pneumatic vehicle tyre with embedded compound-curve springs<br />
(86) PCT/US2006/017893 (87) WO2006/122107<br />
(51) IPC2011.01:B60C7/14<br />
(71) New Tech Tire LLC<br />
(72) Moon, Michael; Corn, Morris;<br />
(31) 05 123808 (32) 6 May 2005 (33) US<br />
(74) SPRUSON & FERGUSON, St Martins Tower, Level 35, 31 Market<br />
Street, Sydney, New South Wales 2000, Australia<br />
(57) A non-pneumatic tyre (30) for a vehicle featuring a body <strong>of</strong> elastic<br />
material and having a circumferentially-extending crown portion featuring<br />
a running surface and circumferentially-extending sidewalls joined to<br />
the crown portion. The side walls terminate in circumferentially-extending<br />
beads which are adapted to engage the rim <strong>of</strong> a vehicle wheel. A<br />
number <strong>of</strong> radially-extending and circumferentially-spaced compoundcurve<br />
springs (32) made <strong>of</strong> a composite material are at least partially<br />
embedded within the crown portion and the sidewalls. The curved springs<br />
have ends terminating within the beads <strong>of</strong> the tyre body. A circumferentially-extending<br />
belt constructed <strong>of</strong> a high-strength and low stretch material<br />
is positioned radially outside <strong>of</strong> the compound-curve springs. The<br />
springs have sidewalls that are generally S-shaped.<br />
(21) 563871 (22) 20 May 2006<br />
(54) Stabile active ingredient complex <strong>of</strong> salts <strong>of</strong> the o-acetylsalicylic acid<br />
with basic amino acids and glycine<br />
(86) PCT/EP2006/004799 (87) WO2006/128600<br />
(51) IPC2011.01:C07C69/86; A61K31/198,60; A61P11/06; A61P9/00<br />
(71) Bayer Schering Pharma Aktiengesellschaft<br />
(72) Franckowiak, Gerhard; Hayauchi, Yukata; Ledwoch, Wolfram;<br />
Schweinheim, Eberhard;<br />
(31) 05 05025283 (32) 2 Jun 2005 (33) DE<br />
(74) HENRY HUGHES, 119-125 Willis Street, Wellington, New Zealand<br />
(57) Disclosed is an active compound complex consisting <strong>of</strong> a salt <strong>of</strong> oacetylsalicylic<br />
acid with a basic amino acid and glycine wherein the compound<br />
complex has a particle size distribution having a mean particle<br />
size <strong>of</strong> less than 100 micrometers.<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 85 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
Also disclosed is the process for making the complex by rapidly combining<br />
o-acetylsalicylic acid and a basic amino acid in water or a watermiscible<br />
organic solvent at a temperature less than or equal to 40 degrees<br />
C to form a homogeneous mixture, cooling the homogeneous mixture<br />
to a temperature <strong>of</strong> from -5 to 10 degrees C, adding thereafter cooled<br />
acetone and a cooled suspension <strong>of</strong> glycine, stirring for at least one hour<br />
and isolating the crystals wherein during crystallization the temperature<br />
is not higher than 5 degrees C.<br />
Further disclosed is a solid product containing the active complex, a pharmaceutical<br />
composition comprising the active complex and the use <strong>of</strong><br />
the active complex to prepare a medicament for the treatment <strong>of</strong> arthritis,<br />
neuralgia, myalgia, migraine, myocardial infarction, stroke, ischemic<br />
heart disease, angina pectoris, bypass operations, PTCA and stent implantation.<br />
(21) 563883 (22) 13 May 2006<br />
(54) Oil suspension concentrate comprising dioxazine pyridylsulfonylureas<br />
(86) PCT/EP2006/004521 (87) WO2006/131187<br />
(51) IPC2011.01:A01N47/36; A01N25/04<br />
(71) Bayer CropScience AG<br />
(72) Sixl, Frank; Schmidt, Annika;<br />
(31) 05 05012120 (32) 4 Jun 2005 (33) EP<br />
(74) HENRY HUGHES, 119-125 Willis Street, Wellington, New Zealand<br />
(57) Disclosed herein is an oil suspension concentrate comprising a) one<br />
or more herbicidally active compounds from the group <strong>of</strong> the dioxazine<br />
pyridylsulfonylureas in suspended form, b) one or more organic solvents,<br />
and c) non-ionic emulsifiers and dispersants. Said oil suspension concentrate<br />
is suitable for use in the crop protection sector.<br />
(21) 563979 (22) 23 May 2006<br />
(54) Solid compositions and methods for treating middle-<strong>of</strong>-the night insomnia<br />
(86) PCT/US2006/020502 (87) WO2006/128022<br />
(51) IPC2011.01:A61K31/415; A61K9/20<br />
(71) Transcept Pharmaceuticals, Inc.<br />
(72) Singh, Nikhilesh; Pather, Sathasivan Indiran;<br />
(31) 05 684842 (32) 25 May 2005 (33) US<br />
(31) 05 741673 (32) 1 Dec 2005 (33) US<br />
(31) 06 788340 (32) 31 Mar 2006 (33) US<br />
(31) 06 788249 (32) 31 Mar 2006 (33) US<br />
(74) SPRUSON & FERGUSON, St Martins Tower, Level 35, 31 Market<br />
Street, Sydney, New South Wales 2000, Australia<br />
(57) Disclosed is the use <strong>of</strong> zolpidem or a salt there<strong>of</strong> for the manufacture<br />
<strong>of</strong> a medicament for use in the treatment <strong>of</strong> a subject who characteristically<br />
awakens from sleep, has difficulty returning to sleep, and wishes to<br />
resume sleep for less than 5 hours, and wherein the medicament comprises<br />
less than 5 mg <strong>of</strong> zolpidem or a pharmaceutically acceptable salt<br />
there<strong>of</strong>.<br />
(21) 564015 (22) 31 May 2006<br />
(54) Bag with leak resistant features<br />
(86) PCT/US2006/020759 (87) WO2006/135562<br />
(51) IPC2011.01:B64F1/02<br />
(71) The Glad Products Company<br />
(72) Broering, Shaun T; Isakson, Cathy Lynn; Waldron, Matthew William;<br />
Mack-Robles, Nancy; O’Hara, Michael Scott; Hnat, Matthew Richard; Hird,<br />
Bryn;<br />
(31) 05 689249 (32) 10 Jun 2005 (33) US<br />
(74) Pizzeys <strong>Patent</strong> and Trade Mark Attorneys, Level 14, ANZ Centre, 324<br />
Queen Street, Brisbane, Queensland 4000, Australia<br />
(57) A leak resistant bag is disclosed. The bag comprises a first pliable<br />
sidewall, a second pliable sidewall, and an absorbent-adhesive mixture.<br />
The second pliable sidewall overlies and joins to the first sidewall along<br />
a closed bottom edge to provide an interior volume. The interior volume<br />
accessible via an opening disposed between the first and second<br />
sidewalls. The absorbent-adhesive mixture comprises an absorbent agent<br />
and an adhesive. The absorbent-adhesive mixture is located on both the<br />
first and second sidewalls along the closed bottom edge.<br />
(21) 564097 (22) 9 Jun 2006<br />
(54) Dried and/or microencapsulated saccharomyces cerevisiae cells with<br />
a high content <strong>of</strong> (S)-(+)-S-adenosyl-L-methionine, process for their preparation,<br />
and compositions containing said cells<br />
(86) PCT/EP2006/005521 (87) WO2006/131382<br />
(51) IPC2011.01:C12N1/18,04; A61K36/064<br />
(71) GNOSIS S.P.A.<br />
(72) Benedetti, Alberto; Sivieri, Lino;<br />
(31) 05 05425413 (32) 9 Jun 2005 (33) EP<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed is a pharmaceutical composition (such as a tablet, a<br />
gastroresistant tablet or a capsule) containing: (a) dried and/or<br />
microencapsulated Saccharomyces cerevisiae cells wherein (R)-(+)-(S)adenosyl-L-methionine<br />
is in a quantity lower than or equal to 10% <strong>of</strong> (S)-<br />
(+)-S-adenosyl-L-methionine, said (S)-(+)-adenosyl-L-methionine being<br />
in the form <strong>of</strong> a free base obtainable from strains <strong>of</strong> Saccharomyces<br />
cerevisiae having a (S)-(+)-S-adenosyl-L-methionine productivity <strong>of</strong> 2.0-<br />
6.0% w/dry w at the end <strong>of</strong> fermentation and 7-20% w/dry w at the end <strong>of</strong><br />
an enrichment stage, and (b) suitable excipients, in dried form or in<br />
microencapsulated form.<br />
(21) 564108 (22) 19 May 2006<br />
(54) Tire fire suppression and vehicle with same<br />
(86) PCT/US2006/019479 (87) WO2006/130363<br />
(51) IPC2011.01:A62C3/07<br />
(71) Kidde Technologies Incorporated<br />
(72) Hodges, Steven Edward; Simpson, Gregory Deane;<br />
(31) 05 141881 (32) 31 May 2005 (33) US<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) A fire suppression apparatus 10 comprises a fire suppressant container<br />
16, at least one temperature sensor 94 positioned away from the<br />
container 16 for sensing an elevated temperature condition at a location,<br />
at least one nozzle 98 positioned away from the container 16 for directing<br />
the suppressant toward the location, and an actuator 20 for connecting<br />
the container 16 to the nozzle 98 for the suppressant to be dispersed<br />
from the nozzle 98. The actuator 20 comprises a chamber 74 that is<br />
sealed from the container, and containing gas at a pressure that is greater<br />
than the ambient air pressure. The chamber 74 has a normally closed<br />
discharge port to atmosphere, which is connected to the temperature<br />
sensor 94 such that the discharge port will open when the sensor 94 is<br />
exposed to the elevated temperature and the gas will be discharged.<br />
The resultant drop in gas pressure in the chamber 74 will cause the<br />
actuator to release the suppressant from the container 16 to the nozzle<br />
98. The apparatus 10 provides a simple, rugged automatic fire suppression<br />
system.<br />
Divisional filed as 590974<br />
(21) 564141 (22) 24 Mar 2006<br />
(54) Two way communication system for monitoring an analyte<br />
(86) PCT/US2006/011090 (87) WO2006/121510<br />
(51) IPC2011.01:A61B5/00<br />
(71) Theranos, Inc.<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 86 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(72) Holmes, Elizabeth A; Roy, Shaunak; Howard, John; Gibbons, Ian;<br />
Wang, Chengwang; Kemp, Tim; Todd, Chris; Oral, Ron; Fenton, Jeff; Qi,<br />
Shize Daniel; Zeng, Shulin;<br />
(31) 05 678801 (32) 9 May 2005 (33) US<br />
(31) 05 705489 (32) 5 Aug 2005 (33) US<br />
(31) 05 717192 (32) 16 Sep 2005 (33) US<br />
(31) 05 721097 (32) 28 Sep 2005 (33) US<br />
(74) SPRUSON & FERGUSON, St Martins Tower, Level 35, 31 Market<br />
Street, Sydney, New South Wales 2000, Australia<br />
(57) A two-way communication system for monitoring an analyte in a body<br />
fluid sample, comprises a reader assembly, an external device configured<br />
to transmit a protocol to the reader assembly, and a fluidic device<br />
configured to be inserted in the reader assembly, where the fluidic device<br />
comprises a sample collection unit configured to collect a body fluid<br />
sample that contains the analyte, an assay assembly containing reactants<br />
that react with the body fluid sample to carry out the test required<br />
by the protocol transmitted from the external device and produce a signal<br />
that indicates the presence <strong>of</strong> the analyte in the sample, and an identifier<br />
that is configured to provide the identity <strong>of</strong> the fluidic device and<br />
also to request the transmission <strong>of</strong> the protocol. The reader assembly is<br />
configured for two-way communication with the external device, and comprises<br />
a programmable processor configured to receive the protocol from<br />
the external device, where the protocol in turn effects a reaction in the<br />
assay assembly for generating the signal, and where the reader assembly<br />
further comprises a detection assembly for detecting the signal, and<br />
a communication assembly for transmitting the signal to the external<br />
device. The system allows remote assessment <strong>of</strong> a patient’s physiological<br />
condition<br />
Divisional filed as 590930<br />
(21) 564146 (22) 24 May 2006<br />
(54) Stable and selective formation <strong>of</strong> Hoogsteen-type triplexes and<br />
duplexes using twisted intercalating nucleic acids (TINA) and process for<br />
the preparation <strong>of</strong> TINA<br />
(86) PCT/DK2006/050022 (87) WO2006/125447<br />
(51) IPC2011.01:C12N15/11; C07H21/00<br />
(71) TINA Holding ApS<br />
(72) Filichev, Vyachelsav; Pedersen, Erik Bjerregaard;<br />
(31) 05 00762 (32) 25 May 2005 (33) DK<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) Provided is a flexible basestacking monomer with the general structure<br />
X – L - I1 – C - I2 wherein X is a backbone monomer unit <strong>of</strong> an<br />
oligonucleotide or an oligonucleotide analogue, or PNA, or PNA analogues,<br />
and wherein X comprises alkylenediol, L is a linker comprising<br />
an alkyl chain, an oxaalkyl chain, an azaalkyl chain, a thiaalkyl chain,<br />
carboxamide group, a thiocarboxamide group, a sulphonamide group or<br />
combinations there<strong>of</strong> and comprises between 0-60 atoms, I1 is a<br />
monocyclic or a polycyclic aromatic ringsystem selected from the group<br />
consisting <strong>of</strong> benzene, naphthalene, azulene and bicyclic heteroaromatic<br />
ring systems, C is a conjugator selected from the group <strong>of</strong> alkyl <strong>of</strong> 1 to 12<br />
carbons, alkeny <strong>of</strong> 2 to 12 carbons, alkynyl <strong>of</strong> 2 to 25 carbons or diazo or<br />
combinations there<strong>of</strong> with a length <strong>of</strong> no more than 25 carbons or/and<br />
nitrogen atoms, I2 is selected from the group <strong>of</strong> bicyclic aromatic<br />
ringsystems, tricyclic aromatic ringsystems, tetracyclic aromatic<br />
ringsystems, pentacyclic aromatic ringsystems and heteroaromatic analogues<br />
there<strong>of</strong> and such compounds with substitutions there<strong>of</strong>. The composition<br />
can be used as a medicament targeted to specific genes or<br />
RNAs depending on the sequence <strong>of</strong> the included oligonucleotide.<br />
(21) 564154 (22) 26 Sep 2006<br />
(54) A survey device<br />
(86) PCT/AU2006/001404 (87) WO2007/041756<br />
(51) IPC2011.01:G01C15/00; G01S5/02; G01V3/00; H04B7/14<br />
(71) Data Info Tech Pty Ltd<br />
(72) Bell, Alexander; Lott, Simon; Murray, Neil;<br />
(31) 05 726070 (32) 11 Oct 2005 (33) US<br />
(31) 05 905602 (32) 11 Oct 2005 (33) AU<br />
(74) DAVIES COLLISON CAVE - SYDNEY, 255 Elizabeth Street, Sydney,<br />
New South Wales 2000, Australia<br />
(57) A handheld survey device, includes an antenna for receiving at least<br />
one wireless signal; at least one interface for receiving environmental<br />
data from at least one interchangeable peripheral device that produces<br />
the environmental data; one or more processors for determining spatial<br />
data using the at least one wireless signal, and for producing collocated<br />
data by combining the spatial data and the environmental data; and an<br />
output device for wirelessly transmitting the collocated data.<br />
(21) 564192 (22) 28 Jun 2006<br />
(54) High performance resin for abrasive products<br />
(86) PCT/US2006/025133 (87) WO2007/005452<br />
(51) IPC2011.01:C08L61/06; B24D11/00; B24D3/28; C08L61/24,28<br />
(71) SAINT-GOBAIN ABRASIVES, INC.<br />
(72) Gaeta, Anthony C; Rice, William C;<br />
(31) 05 695233 (32) 29 Jun 2005 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed is an abrasive product comprising: (a) a plurality <strong>of</strong> abrasive<br />
particles; and (b) an aldehyde resin cured with a polythiol group<br />
selected from the group consisting <strong>of</strong> trimethylolpropane tri(3mercaptopropionate),<br />
trimethylolpropane tri(2-mercaptoacetate), pentaerythritol<br />
tetra(3-mercaptopropionate), pentaerythritol tetra(2mercaptoacetate),<br />
polyol-3-mercaptopropionates, polyol-2mercaptoacetates,<br />
polyester-3-mercaptopropionates, polyester-2mercaptoacetates,<br />
and ethoxylated trimethylolpropane tri(3mercaptopropionate),<br />
and a method <strong>of</strong> preparing the abrasive product<br />
and a method <strong>of</strong> abrading a work surface with the product.<br />
Also disclosed is a curable composition, comprising: (a) a formaldehyde<br />
resin; and (b) a polythiol group selected from the group consisting <strong>of</strong><br />
trimethylolpropane tri(3-mercaptopropionate), trimethylolpropane tri(2mercaptoacetate),<br />
pentaerythritol tetra(3-mercaptopropionate), pentaerythritol<br />
tetra(2-mercaptoacetate), polyol-3-mercaptopropionates, polyol-<br />
2-mercaptoacetates, polyester-3-mercaptopropionates, polyester-2mercaptoacetates<br />
and ethoxylated trimethylolpropan tri-3mercaptopropionate,<br />
a method <strong>of</strong> crosslinking the formaldehyde resin<br />
composition and a crosslinked formaldehyde resin composition.<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 87 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(21) 564258 (22) 22 Jun 2006<br />
(54) Azaindazole compounds and methods <strong>of</strong> use<br />
(86) PCT/US2006/024313 (87) WO2007/002293<br />
(51) IPC2011.01:A61K31/496; C07D487/06<br />
(71) CHEMOCENTRYX, INC.<br />
(72) Zhang, Penglie; Pennell, Andrew M.K.; Wright, John J Kim; Chen,<br />
Wei; Leleti, Manmohan R; Li, Yandong; Li, Lianfa; Xu, Yuan;<br />
(31) 05 693525 (32) 22 Jun 2005 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed are azaindazole compounds and are represented by the<br />
formulas Ia and Ib. The compounds feature a pyrazole fused with a nitrogen<br />
containing heterocycle and an optionally substituted piperazinyl ring.<br />
The substituents are as disclosed in the description.<br />
Also disclosed is a pharmaceutical composition containing a compound <strong>of</strong><br />
formula Ia or Ib and the use <strong>of</strong> a compound <strong>of</strong> formula Ia or Ib in the<br />
manufacture <strong>of</strong> a medicament for treating CCR 1 mediated disease especially<br />
inflammatory conditions and immunoregulatory disorders such<br />
as rheumatoid arthritis, multiple sclerosis, transplant rejection, restenosis,<br />
dermatitis, eczema, urticaria, vasculitis, inflammatory bowel disease, food<br />
allergy, asthma, Alzheimer's disease, Parkinson's disease, psoriasis, lupus<br />
erythematosus, osteoarthritis, stroke, and encephalomyelitis.<br />
(21) 564284 (22) 23 Jun 2006<br />
(54) Baling and bale wrapping apparatus and methods<br />
(86) PCT/IE2006/000069 (87) WO2006/137046<br />
(51) IPC2011.01:A01F15/07,00<br />
(71) Welmount Limited<br />
(72) McHale, Padraic Christopher; Heaney, James John; O’Connor, Patrick<br />
Thomas; Sheridan, Gerard Patrick; Cummins, John Joseph; McHale, Martin<br />
William; McHale, Paul Gerard;<br />
(31) 05 0426 (32) 23 Jun 2005 (33) IE<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) Baling apparatus 1 for forming material into a cylindrical bale and for<br />
wrapping the bale wrapping material 64 comprises a a baler 16 defining<br />
a bale forming chamber defining a longitudinally extending main central<br />
axis, and within which the bale is formed, the baler 16 comprising at<br />
least two segments 21, 22 , at least one <strong>of</strong> which is moveable relative to<br />
the other between a bale forming state where the segments 21, 22 cooperate<br />
to form the bale forming chamber, and a discharge state with<br />
two <strong>of</strong> the segments 21, 22 defining a discharge opening from the bale<br />
forming chamber for accommodating discharge <strong>of</strong> the bale there from, a<br />
bale support located adjacent the baler 16 for receiving a bale discharged<br />
there from and for supporting the bale during wrapping, a first dispenser<br />
63 located to a first side <strong>of</strong> the discharge opening for dispensing the<br />
wrapping material 64 for circumferentially wrapping the bale and a holding<br />
means located to a second side <strong>of</strong> the discharge opening opposite to<br />
the first side there<strong>of</strong>, the holding means being adapted to grip the wrapping<br />
material 64 extending from the first dispenser 63 with the wrapping<br />
material 64 extending across the discharge opening, so that when the<br />
bale is discharged from the bale forming chamber through the discharge<br />
opening onto the bale support, the wrapping material 64 is engaged by<br />
the circumferential surface <strong>of</strong> the bale, and is drawn from the first dispenser<br />
63 onto the bale to extend circumferentially partly around the<br />
circumferential surface <strong>of</strong> the bale.<br />
(21) 564339 (22) 26 Jun 2006<br />
(54) Quinoline derivatives as antibacterial agents<br />
(86) PCT/EP2006/063556 (87) WO2007/000436<br />
(51) IPC2011.01:A61K31/4353; A61P31/04; C07D215/22,227,36<br />
(71) Janssen Pharmaceutica N.V.<br />
(72) Andries, Koenraad Jozef Lodewijk Marcel; Koul, Anil; Guillemont,<br />
Jerome Emile Georges; Motte, Magali Madeleine Simone;<br />
(31) 05 05105769 (32) 28 Jun 2005 (33) EP<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) Disclosed is the use <strong>of</strong> a quinoline derivative compound <strong>of</strong> formula Ia<br />
or Ib in the manufacture <strong>of</strong> a medicament for the treatment <strong>of</strong> a bacterial<br />
infection. The substituents are as disclosed in the description.<br />
Also disclosed is a compound <strong>of</strong> formula Ia.<br />
Further disclosed is a combination <strong>of</strong> a compound <strong>of</strong> formula Ia and another<br />
antibacterial agent; a pharmaceutical composition containing a<br />
compound <strong>of</strong> formula Ia; and the use <strong>of</strong> the combination <strong>of</strong> composition<br />
to treat bacterial infection other than Mycobacterial infection. Particular<br />
bacterial infections are infection with Staphylococci, Enterococci or Streptococci<br />
especially the infection is an infection with methicillin resistant<br />
Staphylococcus aureus (MRSA), methicillin resistant coagulase negative<br />
staphylococci (MRCNS), penicillin resistant Streptococcus<br />
pneumoniae or multiple resistant Enterococcus faecium.<br />
(21) 564340 (22) 26 Jun 2006<br />
(54) Quinoline derivatives as antibacterial agents<br />
(86) PCT/EP2006/063552 (87) WO2007/000434<br />
(51) IPC2011.01:A61K31/4353; A61P31/04; C07D215/227,36<br />
(71) Janssen Pharmaceutica N.V.<br />
(72) Andries, Koenraad Jozef Lodewijk Marcel; Koul, Anil; Guillemont,<br />
Jerome Emile Georges; Motte, Magali Madeleine Simone; Lancois, David<br />
Francis Alain;<br />
(31) 05 05105755 (32) 28 Jun 2005 (33) EP<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 88 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(57) Disclosed is the use <strong>of</strong> quinoline compounds <strong>of</strong> formula (Ia) and (Ib)<br />
a N-oxide, tautomeric or a stereochemically isomeric form there<strong>of</strong>, wherein<br />
the substituents are as defined in the specification, for the treatment <strong>of</strong><br />
bacterial infections such as infection with Staphylococci, Enterococci or<br />
Streptococci.<br />
(21) 564376 (22) 15 Jun 2006<br />
(54) Method for the synthesis <strong>of</strong> anthocyanins<br />
(86) PCT/GB2006/002172 (87) WO2006/134352<br />
(51) IPC2011.01:C07H17/04; C07H15/18<br />
(71) Biosynth AS<br />
(72) Bakstad, Einar;<br />
(31) 05 0512206 (32) 15 Jun 2005 (33) GB<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) Disclosed is a method for preparing an Eastern portion <strong>of</strong> anthocyanin<br />
comprising reacting an alpha functionalised ketone starting material<br />
<strong>of</strong> general formula S-1, with a sugar anion <strong>of</strong> general formula XO-.<br />
Also disclosed is the compound <strong>of</strong> formula S-1, wherein LG is Br or I and<br />
R1, R2 and R3 each denote a benzyloxy, or R1 denotes H and R2 and<br />
R3 together denote diphenylmethylenedioxy. Also disclosed are compounds<br />
<strong>of</strong> formula (i), (ii) or (iii).<br />
(21) 564378 (22) 16 Jun 2006<br />
(54) Methods and systems for delivering foamed beverages from liquid<br />
concentrates through a dispenser machine<br />
(86) PCT/EP2006/005785 (87) WO2006/136329<br />
(51) IPC2011.01:A47J31/00,40<br />
(71) Nestec S.A.<br />
(72) Saggin, Raffaella; Leser, Martin; Bezelgues, Jean-Baptiste; Livings,<br />
Simon; Sher, Alexander A;<br />
(31) 05 156922 (32) 20 Jun 2005 (33) US<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) A method and system to deliver foamed beverages from liquid<br />
concentrate(s) through a dispenser machine is disclosed. In an embodiment,<br />
the method and system for improving foam quality by generating<br />
foam with the desired texture, stability and bubble size distribution comprises<br />
use <strong>of</strong> a low viscous liquid(s) to generate a primary foam, which is<br />
then stabilized by mixing it with liquid(s) <strong>of</strong> higher viscosity. To create<br />
high quality foam, different dosing protocols including two approaches<br />
such as delivery <strong>of</strong> foaming liquid concentrates at different concentration,<br />
or getting different concentration by varying water dosing times and/<br />
or flow rates were used. Positive results were found for the dispensing<br />
systems using milk and other liquid concentrates at specific dispensing<br />
conditions (flow rates and times).<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 89 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(21) 564496 (22) 3 Jul 2006<br />
(54) An apparatus and process for conversion <strong>of</strong> biomass/waste into bioorganic<br />
soil enricher & conditioner and fuel<br />
(86) PCT/IN2006/000235 (87) WO2007/034504<br />
(51) IPC2011.01:C05F9/02; B01F7/04,12; C05F11/08; C05F9/04<br />
(71) Excel Industries Limited<br />
(72) Shr<strong>of</strong>f, Ashwin Champraj; Jawdekar, Mohan Chintopant;<br />
(31) 05MU 823 (32) 5 Jul 2005 (33) IN<br />
(74) JAMES & WELLS, Level 12, KPMG Centre, 85 Alexandra Street,<br />
Hamilton, New Zealand<br />
(57) The disclosure relates to a device and a process for conversion <strong>of</strong><br />
biodegradable waste into organic fertilizer and fuel for heating. The organic<br />
fertilizer produced by the disclosed method provides nutrients to<br />
plants and at the same time improves moisture retaining capacity <strong>of</strong> the<br />
soil, prevents erosion and leaching. Particularly disclosed is an apparatus<br />
for treating biomass/organic waste comprising a container incorporating<br />
a shaft at the axis, affixed on which are plough type blades and an<br />
opening preferably at the top side for feeding the material; a chopper<br />
assembly, at least the blades <strong>of</strong> the said chopper assembly inserted into<br />
the container; a discharge assembly preferably connected at the bottom<br />
side <strong>of</strong> the container; a door at the connecting junction <strong>of</strong> the container<br />
and the discharge assembly which can be opened and closed, the said<br />
door may be a part <strong>of</strong> the container or the discharge assembly. Also<br />
disclosed is a process for converting bio-degradable waste/biomass<br />
material into organic fertilizer comprising feeding the said material into<br />
the container <strong>of</strong> said apparatus and chopping the material; adding a microbial<br />
culture or substance obtained there from; optionally adding a<br />
moisture absorbing substance; running the motor for mixing, taking out<br />
the material preferably on the ground to make a heap and ensuring aerobic<br />
conditions until the material matures into an organic fertilizer. The<br />
bio-stabilised material produced using said apparatus can be converted<br />
into fuel by spreading the material in a suitable mould, pressing and cutting<br />
the material into pieces <strong>of</strong> suitable size; and drying the material.<br />
(21) 564689 (22) 23 May 2006<br />
(54) Novel piperidine carboxylic acid amide derivatives<br />
(86) PCT/IB2006/051641 (87) WO2006/129237<br />
(51) IPC2011.01:C07D471/08; A61K31/451; A61P9/00; C07D401/10,12;<br />
C07D211/78<br />
(71) Actelion Pharmaceuticals Ltd.<br />
(72) Bezencon, Olivier; Boss, Christoph; Bur, Daniel; Chen, Austin Chih-<br />
Yu; Corminboeuf, Olivier; Dube, Daniel; Fischli, Walter; Grisostomi,<br />
Corinna; Remen, Lubos; Richard-Bildstein, Sylvia; Sifferlen, Thierry;<br />
Therien, Michel; Weller, Thomas;<br />
(31) PCT/EP2005/0005732 (32) 27 May 2005 (33) EP<br />
(31) PCT/IB2006/050134 (32) 13 Jan 2006 (33) IB<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed are piperidine carboxylic acid amide compounds <strong>of</strong> formula<br />
(I) wherein R1 is cycloalkyl and the remaining substitutents are as<br />
defined in specification. Also disclosed are pharmaceutical compositions<br />
containing said compounds and their use as rennin inhibitors and<br />
treating diseases such as cardiovascular events and renal insufficiency.<br />
(21) 564886 (22) 15 Aug 2006<br />
(54) Humidifier for CPAP device with tub base plate forced into engagement<br />
with heater plate by cradle retaining structure<br />
(86) PCT/AU2006/001170 (87) WO2007/019625<br />
(51) IPC2011.01:A61M16/16<br />
(71) RESMED LIMITED<br />
(72) SMITH, Ian Malcolm; SNOW, John Michael; LITHGOW, Perry David;<br />
KAO, Dan;<br />
(31) 05 707948 (32) 15 Aug 2005 (33) US<br />
(74) JAMES & WELLS, Level 12, KPMG Centre, 85 Alexandra Street,<br />
Hamilton, New Zealand<br />
(57) A CPAP device includes a humidifier including humidifier tub having a<br />
heat conducting base plate; and a cradle to support the humidifier tub in<br />
an operative position. The cradle may also support a flow generator in<br />
operative relation to the humidifier tub. The cradle includes a heater plate<br />
in communication with the heat conducting base plate <strong>of</strong> the humidifier<br />
tub in use. The cradle further includes a retaining mechanism to retain<br />
the humidifier tub in the cradle, the retaining mechanism being structured<br />
to force the base plate into engagement with the heater plate. The<br />
humidifier and/or flow generator may include various features to manage<br />
inadvertent back-spill <strong>of</strong> water from the humidifier to the flow generator.<br />
Divisional filed as 586325<br />
(21) 564908 (22) 7 Sep 2005<br />
(54) N-Phenyl-2-pyrimidine-amine derivatives and process for the preparation<br />
there<strong>of</strong><br />
(86) PCT/KR2005/002962 (87) WO2007/018325<br />
(51) IPC2011.01:C07D239/02; A61K31/425,44,4965,505; A61P35/00;<br />
C07D239/28; C07D401/02; C07D417/00<br />
(71) IL-YANG PHARM. CO., LTD<br />
(72) Kim, Dong-Yeon; Cho, Dae-Jin; Lee, Gong-Yeal; Kim, Hong-Youb;<br />
Woo, Seok-Hun; Kim, Yong-Seok; Lee, Sun-Ahe; Han, Byoung-Cheol;<br />
(31) 05 050071656 (32) 5 Aug 2005 (33) KR<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) Disclosed are N-phenyl-2-pyrimidine-amine derivatives <strong>of</strong> formula (1)<br />
wherein one <strong>of</strong> R4 or R5 must be a radical <strong>of</strong> formula (2). A process for<br />
preparing the said compounds is also disclosed. Also disclosed is the<br />
use <strong>of</strong> the said compound in a pharmaceutical composition for the manufacture<br />
<strong>of</strong> a medicament for the treatment <strong>of</strong> cancer.<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 90 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(21) 564954 (22) 14 Jun 2006<br />
(54) Method <strong>of</strong> treating or preventing benign prostatic hyperplasia using<br />
modified pore-forming proteins<br />
(86) PCT/CA2006/000971 (87) WO2006/133553<br />
(51) IPC2011.01:C07K14/195; A61K35/74; A61K38/16<br />
(71) Protox Therapeutics Incorporated<br />
(72) Buckley, James Thomas;<br />
(31) 05 690269 (32) 14 Jun 2005 (33) US<br />
(74) SPRUSON & FERGUSON, St Martins Tower, Level 35, 31 Market<br />
Street, Sydney, New South Wales 2000, Australia<br />
(57) Provided is the use <strong>of</strong> a modified pore-forming protein for the preparation<br />
<strong>of</strong> a medicament for the treatment <strong>of</strong> benign prostatic hyperplasia<br />
(BPH), wherein said modified pore-forming protein is derived from a naturally-occurring<br />
pore-forming proaerolysin protein and comprising one or<br />
more prostate-selective modifications selected from: an activation sequence<br />
cleavable by a prostate-specific protease, and one or more prostate-specific<br />
targeting domains capable <strong>of</strong> selectively targeting prostate<br />
cells, wherein said modified pore-forming protein is capable <strong>of</strong> selectively<br />
killing prostate cells. Further provided is the use <strong>of</strong> the medicament<br />
for treating BPH in non-human animals.<br />
(21) 565001 (22) 9 Aug 2006<br />
(54) Improvements in and relating to wool treatment<br />
(86) PCT/GB2006/002955 (87) WO2007/017668<br />
(51) IPC2011.01:D06M13/46; D06M11/32,38,50<br />
(71) PERACHEM LIMITED<br />
(72) Lewis, David Malcolm; Hawkes, Jamie Anthony;<br />
(31) 05 0516392 (32) 10 Aug 2005 (33) GB<br />
(31) 05 0524371 (32) 30 Nov 2005 (33) GB<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed is a method <strong>of</strong> treating a wool material, the method comprising<br />
the steps <strong>of</strong>: (a) contacting the wool material with a cationic surfactant;<br />
and (b) contacting the wool material with a nucleophile; wherein<br />
steps (a) and (b) are performed simultaneously at a pH <strong>of</strong> at least 8<br />
wherein the nucleophile is selected from hydrogen peroxide and its derivatives,<br />
the perhydroxy anion, the superoxide anion, a per-acid, a<br />
polyper-acid, an alkali metal hydroxide or ammonium hydroxide, the hydroxyl<br />
anion, hydroxylamine, an alkanolamine, an alcoholate, an amine,<br />
a phenol, thiocyanate or any mixture there<strong>of</strong>; and wherein the method<br />
comprises a continuous process. Also disclosed is a wool material that<br />
is treated by the above method.<br />
(21) 565062 (22) 24 Jul 2006<br />
(54) Benzylpiperazine derivates and their use in treating conditions mediated<br />
by GPR38 receptors<br />
(86) PCT/EP2006/007390 (87) WO2007/012479<br />
(51) IPC2011.01:C07D401/10; A61K31/496; A61P1/08<br />
(71) Glaxo Group Limited<br />
(72) Johnson, Christopher Norbert; Macpherson, David Timothy; Stanway,<br />
Steven James; Stemp, Ge<strong>of</strong>frey; Thompson, Mervyn; Westaway, Susan<br />
Marie;<br />
(31) 05 0515381 (32) 26 Jul 2005 (33) GB<br />
(31) 06 0611469 (32) 9 Jun 2006 (33) GB<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed is a compound including a piperidine and a piperazine as<br />
shown in formula (I), or a salt there<strong>of</strong>, wherein A is phenyl or pyridine,<br />
and the other substituents are as defined in the specification.<br />
Also disclosed is the use <strong>of</strong> the compound to treat conditions mediated by<br />
GPR38 receptors, such as gastroesophageal reflux disorders, functional<br />
dyspepsia, irritable bowel syndrome, constipation, intestinal pseudo-obstruction,<br />
paralytic ileus following surgery or other manipulation, emesis,<br />
gastric stasis or hypomotility caused by various diseases such as diabetes<br />
and/ or by the administration <strong>of</strong> other drugs, Crohn's disease, colitis,<br />
cachexia associated with advanced diseases such as cancer and/or the<br />
treatment there<strong>of</strong>, appetite/metabolism related cachexia, and incontinence.<br />
Also disclosed is a method to synthesise the compound, and intermediates<br />
useful in that method.<br />
(21) 565150 (22) 25 Jul 2006<br />
(54) Pyrazine derivatives useful as adenosine receptor antagonists<br />
(86) PCT/EP2006/007318 (87) WO2007/017096<br />
(51) IPC2011.01:C07D401/04,14; C07D413/14; A61K31/497; C07D403/<br />
04; C07D417/04; A61K31/506; C07D405/14; C07D417/14; A61P11/06;<br />
C07D409/14; C07D487/04<br />
(71) LABORATORIOS ALMIRALL, S.A.<br />
(72) Vidal Juan, Bernat; Esteve Trias, Cristina; Soca Pueyo, Lidia;<br />
Eastwood, Paul Robert;<br />
(31) 05 0501876 (32) 29 Jul 2005 (33) ES<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed is a secondary pyrazine amine <strong>of</strong> formula (I) wherein: A<br />
represents an aryl or heteroaryl group, B represents a nitrogen-containing<br />
heteroaryl group and R1 and R2 are defined in the specification and<br />
the pharmaceutically acceptable salts and N-oxides there<strong>of</strong>. Also disclosed<br />
is a composition comprising said amine and the use <strong>of</strong> said amine<br />
in the treatment <strong>of</strong> a condition susceptible <strong>of</strong> being improved by antagonism<br />
with the A2B adenosine receptor for example, hypertension and<br />
inflammation.<br />
(21) 565162 (22) 19 Oct 2005<br />
(54) Catalyzed decomposing foam for encapsulating space-based kinectic<br />
objects<br />
(86) PCT/US2005/037586 (87) WO2007/001419<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 91 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(51) IPC2011.01:B64G1/00,22,64; F41H11/02; F42B12/56<br />
(71) Raytheon Company<br />
(72) Duden, Quenten E; Mense, Allan T;<br />
(31) 04 969724 (32) 20 Oct 2004 (33) US<br />
(74) JAMES & WELLS, Level 12, KPMG Centre, 85 Alexandra Street,<br />
Hamilton, New Zealand<br />
(57) Disclosed is a kinetic media payload <strong>of</strong> a weapon system which uses<br />
kinetic media to intercept a target, the payload being suitable for launching<br />
into space by a vehicle. The kinetic media payload comprises kinetic<br />
media which is at least partially surrounded by foam which decomposes<br />
in the presence <strong>of</strong> high energy electromagnetic radiation.<br />
(21) 565205 (22) 16 Jun 2006<br />
(54) Cell signalling genes from plants (Eucalyptus and Pinus species) and<br />
related methods<br />
(86) PCT/US2006/023561 (87) WO2006/138606<br />
(51) IPC2011.01:A01H5/00; A01H7/00; C12N15/82; C12N5/04; C12P21/<br />
06; C12N1/20; C12N15/00; C07H21/02; C12N9/00; C07H21/04; A01H1/<br />
00<br />
(71) ArborGen, LLC<br />
(72) Chang, Shujun; Connett, Marie B; Emerson, Sarah Jane; Forster,<br />
Richard L; Gause, Katrina; Havukkala, Ilkka; Higgins, Colleen; Kodrzycki,<br />
Robert John;<br />
(31) 05 691398 (32) 17 Jun 2005 (33) US<br />
(74) KNIGHTSBRIDGE PATENT ATTORNEYS, Level 14, 200 Queen<br />
Street, Melbourne, Victoria 3000, Australia<br />
(57) Disclosed is a polyphosphoinositide binding protein from Pinus Radiata.<br />
The protein is associated with plant cell signalling and can be<br />
used to control plant phenotype.<br />
(21) 565218 (22) 25 Jul 2006<br />
(54) Liquid natural gas processing for hydrocarbons heavier than methane<br />
(86) PCT/US2006/028822 (87) WO2007/014209<br />
(51) IPC2011.01:F25J3/02<br />
(71) HOWE-BAKER ENGINEERS, LTD<br />
(72) Schroeder, Scott; Reddick, Kenneth; Belhateche, Noureddine;<br />
(31) 05 188961 (32) 25 Jul 2005 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) A process for the recovery <strong>of</strong> natural gas liquids (NGL) from liquefied<br />
natural gas (LNG) is disclosed. The LNG feed stream is subjected to a<br />
two stage separation process where the bottoms from the first stage<br />
separation containing C2+ hydrocarbons is split into two portions, with<br />
one portion being heated and used as a reflux during the second stage<br />
separation to recover the NGL product. Particularly disclosed is a process<br />
<strong>of</strong> recovering hydrocarbons heavier than methane from liquefied<br />
natural gas (LNG) comprising, a) pumping liquid, low pressure LNG to a<br />
pressure <strong>of</strong> greater than 100 psia; (b) directing the pressurized liquid<br />
LNG from step (a) to a cold box where it is heat exchanged to increase<br />
its temperature; (c) directing the heat exchanged pressurized liquid LNG<br />
from step b) to a separator where, in combination with a first and second<br />
reflux, a separator overhead is produced along with a separator bottoms;<br />
(d) pressurizing the separator bottoms and then splitting the pressurized<br />
separator bottoms into first and second portions; (e) directing<br />
the first portion <strong>of</strong> pressurized separator bottoms to a deethanizer as a<br />
reflux stream; (f) heating the second portion <strong>of</strong> pressurized separator<br />
bottoms by directing the second portion to the cold box; (g) directing the<br />
heated second portion <strong>of</strong> pressurized separator bottoms to the<br />
deethanizer; (h) removing hydrocarbons heavier than methane as<br />
deethanizer bottoms; (i) directing a deethanizer overhead as the second<br />
feed to the separator; (j) removing the separator overhead from the separator<br />
and compressing the separator overhead prior to introduction into<br />
the cold box and heat exchanging with the pressurized liquid LNG to<br />
produce a re-liquefied pressurized LNG; and (k) separating a portion <strong>of</strong><br />
the re-liquefied pressurized LNG for use as the first reflux.<br />
(21) 565247 (22) 20 Jul 2006<br />
(54) Process for the production drospirenone utilising the metal-free oxidation<br />
<strong>of</strong> 17-(3-hydroxypropyl)-3,17-dihydroxyandrostanes with TEMPO<br />
(86) PCT/EP2006/007287 (87) WO2007/009821<br />
(51) IPC2011.01:C07J53/00; C07J19/00; C07J21/00<br />
(71) BAYER SCHERING PHARMA AKTIENGESELLSCHAFT<br />
(72) Seba, Hartmut; Seilz, Carsten;<br />
(31) 05 05090214 (32) 21 Jul 2005 (33) EP<br />
(31) 05 185984 (32) 21 Jul 2005 (33) US<br />
(74) HENRY HUGHES, 119-125 Willis Street, Wellington, New Zealand<br />
(57) Disclosed is a process for the production <strong>of</strong> a 3-oxo-pregnane-21,17carbolactone<br />
<strong>of</strong> formula II, comprising the reaction <strong>of</strong> a compound <strong>of</strong><br />
formula I, with at least 3 molar equivalents <strong>of</strong> an organic or inorganic<br />
hypochlorite as oxidizing agent in the presence <strong>of</strong> catalytic amounts <strong>of</strong> a<br />
2,2,6,6-tetramethylpiperidine-N-oxide derivative (TEMPO) at a pH <strong>of</strong> at<br />
least 8.0, wherein R5 is hydrogen or hydroxy; R6a is hydrogen, or together<br />
with R7a a -CH2 group; R6b is hydrogen, or together with R7b a<br />
-CH2 group or a double bond; R7a is hydrogen, alkyl, alkoxycarbonyl,<br />
thioacyl or together with R6a a -CH2 group, R7b is hydrogen, or together<br />
with R6b a -CH2 group or a double bond; R9 is hydrogen or together with<br />
R11 is a double bond, or together with R11 is an epoxy group -O-; R10 is<br />
hydrogen, methyl, or ethyl; R11 is hydrogen, or together with R9 a double<br />
bond or together with R9 is an epoxy group -O-; R13 is hydrogen, methyl<br />
or ethyl; R15 is hydrogen, alkyl, or together with R16 a -CH2 group or a<br />
double bond; R16 is hydrogen, or together with R15 a -CH2 group or a<br />
double bond. Also disclosed is a process for the production <strong>of</strong> a 3-oxopregn-4-ene-21,17-carbolactone<br />
<strong>of</strong> formula III which comprises the elimination<br />
<strong>of</strong> water from a compound <strong>of</strong> formula II at a pH <strong>of</strong> less than 5,<br />
optionally in the presence <strong>of</strong> an acid. Further disclosed is the use and<br />
preparation <strong>of</strong> 6b,7b;15b,16b-dimethylene-3-oxo-17a-pregnan-5b-ol-<br />
21,17-carbolactone-dichloromethane hemisolvate <strong>of</strong> formula (IV).<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 92 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(21) 565504 (22) 2 Aug 2006<br />
(54) Antitumoral bioconjugates <strong>of</strong> hyaluronic acid or its derivatives obtained<br />
by indirect chemical conjugation<br />
(86) PCT/EP2006/007717 (87) WO2007/014784<br />
(51) IPC2011.01:A61K47/48<br />
(71) FIDIA FARMACEUTICI S.P.A.<br />
(72) Renier, Davide; Bettella, Fabio;<br />
(31) 05 PD A 0242 (32) 3 Aug 2005 (33) IT<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed is a chemical-pharmaceutical conjugates <strong>of</strong> hyaluronic acid<br />
and/or its derivatives obtained through an indirect binding between the<br />
polysaccharide and an alkaloid drug with an antitumoral action, via a<br />
molecular spacer which forms an ester or amide bond with the carboxylic<br />
group <strong>of</strong> HA and/or its derivative. Also disclosed is a composition<br />
comprising said conjugate, the use <strong>of</strong> said conjugate in the preparation<br />
<strong>of</strong> pharmaceutical compositions for the treatment <strong>of</strong> cancer and a process<br />
for the preparation <strong>of</strong> the said conjugates.<br />
(21) 565553 (22) 11 Aug 2006<br />
(54) A device for capturing energy from a fluid flow having a lift generating<br />
element with a lunate surface adapted to drive the device in oscillatory<br />
motion<br />
(86) PCT/AU2006/001148 (87) WO2007/019607<br />
(51) IPC2011.01:E02B9/08; F03B13/18,26; F03D5/00<br />
(71) BioPower Systems Pty. Ltd.<br />
(72) Finnigan, Timothy Donegal;<br />
(31) 05 904358 (32) 12 Aug 2005 (33) AU<br />
(31) 06 904032 (32) 26 Jul 2006 (33) AU<br />
(74) F B RICE & CO, Level 23, 44 Market Street, Sydney, New South<br />
Wales 2000, Australia<br />
(57) A device for capturing energy from a fluid flow is disclosed. The device<br />
comprises a base, a longitudinal member, a lift generating element,<br />
and an energy transfer mechanism. The base is stationary and is mounted<br />
relative to the fluid flow. The member has a longitudinal axis, and is<br />
movably connected to the base. The lift generating element, connected<br />
to the member, has a leading edge and a trailing edge and a generally<br />
lunate surface extending therebetween. The lift generating element is<br />
movable relative to the direction <strong>of</strong> the fluid flow to vary a direction <strong>of</strong> lift<br />
produced by the lift generating element as fluid flows around it. The generating<br />
element drives the member in an oscillatory motion relative to the<br />
base. An energy transfer mechanism is attached to the member and is<br />
driven by the oscillation <strong>of</strong> the member.<br />
Divisional filed as 586985<br />
(21) 565714 (22) 16 Aug 2006<br />
(54) Dual gland air inversion and steam cure <strong>of</strong> cured in place liners<br />
(86) PCT/US2006/031927 (87) WO2007/022232<br />
(51) IPC2011.01:F16L55/165<br />
(71) INA ACQUISITION CORP.; INSITUFORM HOLDINGS (UK) LIMITED<br />
(72) Hirtz, Steve J; Driver, Franklin Thomas; Polivka, Richard C; Blasczyk,<br />
James H; Birchler, Neil; Costa, Kyle;<br />
(31) 05 708934 (32) 17 Aug 2005 (33) US<br />
(31) 06 504909 (32) 16 Aug 2006 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Installation <strong>of</strong> a flexible cured in place liner is disclosed by inverting<br />
the liner with air and curing the liner with steam introduced through a<br />
perforated lay flat hose without deflating the liner between the inversion<br />
and cure. The installation is performed with an apparatus having two<br />
independently operable glands with at least one fluid inlet port installed<br />
on the line downstream <strong>of</strong> the second gland liner. As the liner reaches<br />
the distal end <strong>of</strong> the conduit to be lined, it enters a sample and porting<br />
pipe with an exhaust pipe gland and exhaust pipe and it is pierced by a<br />
rigid porting tool. Steam is then introduced into the lay flat hose to cure<br />
the resin and is exhausted through an exhaust hose connected to a controllable<br />
exhaust pipe. After curing steam is replaced with air to cool the<br />
liner, the ends are cut to restore service through the host pipe.<br />
(21) 565726 (22) 23 Jun 2006<br />
(54) Low-temperature motor compressor unit with continuous ‘cold’ combustion<br />
at constant pressure and with active chamber<br />
(86) PCT/FR2006/001444 (87) WO2006/136728<br />
(51) IPC2011.01:F01B17/02; F02B29/04; F02G1/02,04; F02G3/02; F02G1/<br />
00; F02G3/00<br />
(71) MDI Motor Development International S.A.<br />
(72) Negre, Guy; Negre, Cyril;<br />
(31) 05 0506437 (32) 24 Jun 2005 (33) FR<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 93 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(74) JAMES & WELLS, Level 12, KPMG Centre, 85 Alexandra Street,<br />
Hamilton, New Zealand<br />
(57) Low-temperature, continuous cold combustion, constant pressure,<br />
active chamber motor-compressor unit, operating with working compressed<br />
air or gas comprises a piston travel control device that momentarily<br />
stops a main engine piston 1 at its top dead centre position, as well<br />
as a variable volume active chamber fitted with the means to produce<br />
work during filling, joined to and in permanent contact with the space<br />
contained above the main engine piston by means <strong>of</strong> a passage 12, as<br />
well as an integrated or non-characterized compression device and a<br />
cold chamber 29 able to reduce to very low temperatures the atmospheric<br />
air or gas that supplies the input 28 <strong>of</strong> the compression device.<br />
The compression device then forces this low temperatures working compressed<br />
air or gas into an external work capacity or combustion chamber<br />
19 fitted with a constant pressure heating device 19A where the working<br />
compressed air or gas will increase in volume before the working compressed<br />
air or gas is transferred into an expansion device that includes<br />
an active chamber 13. When the main engine piston is stopped at the<br />
top dead centre position, the expansion chamber will be at its smallest<br />
volume. The compressed air or gas will increase its volume and thus<br />
produce work by pushing the pressure piston 14. The compressed air or<br />
gas contained in the expansion chamber then expands in the engine<br />
cylinder thus pushing the main engine piston 1 downwards along its travel<br />
and supplying work in turn. During the exhaust stroke the main engine<br />
piston 1 will travel upwards again reducing the variable volume <strong>of</strong> the<br />
expansion chamber to its lowest value to restart a complete work cycle.<br />
(21) 565727 (22) 12 Jun 2006<br />
(54) Multiple nozzle venturi system for watercraft<br />
(86) PCT/US2006/023026 (87) WO2007/005209<br />
(51) IPC2011.01:B63H5/16; B63H11/00; B63H5/00,07,15<br />
(71) Marine Propulsion Technologies, Inc,<br />
(72) Smith, Terrence L; Schultz, Wilderich C;<br />
(31) 05 696285 (32) 5 Jul 2005 (33) US<br />
(74) JAMES & WELLS, Level 12, KPMG Centre, 85 Alexandra Street,<br />
Hamilton, New Zealand<br />
(57) A multiple nozzle Venturi system 10A for watercraft comprises a first<br />
hemispherical component and a second hemispherical component, both<br />
the first hemispherical component and the second hemispherical component<br />
including a hemispherical structural ring 18 and two or more hemispherical<br />
nozzle rings 22, 24 the first hemispherical component and the<br />
second hemispherical component including two or more ring connecting<br />
fin struts 16 spanning, separating and integrated into the structural ring<br />
18 and the two or more nozzle rings 22, 24 the first hemispherical component<br />
and the second hemispherical component further including an<br />
upper mounting plate 26 and a lower mounting plate 31 spanning, separating<br />
and integrated into the structural ring 18 and the two or more nozzle<br />
rings 22, 24 and a skeg shield 32 including a T-shaped skid plate 36<br />
sandwiched between the lower mounting plate 31 <strong>of</strong> the first hemispherical<br />
component and the second hemispherical component including an<br />
upper portion and a lower portion where the lower portion is removably<br />
attachable to the lower mounting plate <strong>of</strong> both the first and second hemispherical<br />
components. The T-shaped skid plate 36 further includes a<br />
skeg lock 42 adjustable in construction to fit a skeg located on the lower<br />
portion <strong>of</strong> a watercraft motor, where the skeg lock 42 functions to stabi-<br />
lize the watercraft when in motion in reverse, and reinforces any fasteners<br />
used to attached the skeg shield 32, the T-shaped skid plate 36 and<br />
the lower mounting plate 31, and where the upper mounting plate 26, the<br />
lower mounting plate 31, the skeg shield 32, and the skeg lock 42, are<br />
fastened to the watercraft motor using steel fasteners.<br />
(21) 565729 (22) 27 Jul 2006<br />
(54) Axle spindle and wheel end assembly with inboard and outboard bearings<br />
immovably mounted on axle spindle<br />
(86) PCT/US2006/029205 (87) WO2007/030220<br />
(51) IPC2011.01:B60B27/00<br />
(71) Hendrickson International Corporation<br />
(72) White, Jay;<br />
(31) 05 713887 (32) 2 Sep 2005 (33) US<br />
(74) FISHER ADAMS KELLY, Level 29, 12 Creek Street, Brisbane, Queensland<br />
4000, Australia<br />
(57) An axle for a heavy-duty vehicle extends transversely across the vehicle<br />
and includes a central portion. Each one <strong>of</strong> a pair <strong>of</strong> relatively short<br />
and lightweight axle spindles is connected to and extends outboardly<br />
from a respective end <strong>of</strong> the axle central portion. A wheel end assembly<br />
is rotatably mounted on each axle spindle. Each wheel end assembly<br />
includes spaced-apart inboard and outboard bearings that are immovably<br />
mounted on its respective axle spindle, and preferably are standard<br />
heavy-duty vehicle stock-type bearings. A relatively short and lightweight<br />
wheel hub is rotatably mounted on the bearings so that the wheel end<br />
assembly selectively accommodates a dual-wheel, standard-tire configuration<br />
and a single-wheel, wide-tire configuration, including a two-inch<br />
<strong>of</strong>fset wheel.<br />
(21) 565798 (22) 13 Jul 2006<br />
(54) Wave protection structure, method for producing a toe element for a<br />
wave protection structure, and method for producing a wave protection<br />
structur<br />
(86) PCT/NL2006/000366 (87) WO2007/011208<br />
(51) IPC2011.01:E02B3/12,14<br />
(71) Koninklijke BAM Groep N.V<br />
(72) Van Den Berge, Arnoud; Reedijk, Jan Sebastiaan; Canto, Rolf Rainer;<br />
(31) 05 1029538 (32) 15 Jul 2005 (33) NL<br />
(74) DAVIES COLLISON CAVE - MELBOURNE, 1 Nicholson Street, Melbourne,<br />
Victoria, Australia<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 94 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(57) Wave protection structure for a slope, where the slope merges into a<br />
bed at the location <strong>of</strong> a toe, is disclosed. The wave protection structure<br />
comprises a plurality <strong>of</strong> wave protection elements <strong>of</strong> the interlocking type<br />
and a plurality <strong>of</strong> toe elements. The wave protection elements are each<br />
provided with a plurality <strong>of</strong> projections, where the projections extend in a<br />
plurality <strong>of</strong> planes to form a three-dimensional structure for the dissipation<br />
<strong>of</strong> wave energy. Also, the wave protection elements may engage in<br />
spaces between the projections <strong>of</strong> one or more adjacent wave protection<br />
elements in such a manner that the freedom <strong>of</strong> movement <strong>of</strong> the<br />
wave protection elements is limited in three dimensions. The wave protection<br />
elements on the slope are provided in a substantially regular imaginary<br />
grid, with a horizontal grid spacing between the centres <strong>of</strong> gravity<br />
<strong>of</strong> the wave protection elements. The toe elements extend in a longitudinal<br />
direction <strong>of</strong> the toe in order to counteract displacement <strong>of</strong> the<br />
wave protection elements from the slope to the bed, and are <strong>of</strong> a shape<br />
which deviates from the shape <strong>of</strong> the wave protection elements. The<br />
centres <strong>of</strong> gravity <strong>of</strong> the toe elements, in the longitudinal direction <strong>of</strong> the<br />
toe, are provided at substantially the same horizontal grid spacing from<br />
one another as the wave protection elements.<br />
(21) 565873 (22) 8 Aug 2006<br />
(54) A storage racking beam with a horizontal loading capacity independent<br />
<strong>of</strong> its vertical loading capacity<br />
(86) PCT/AU2006/001126 (87) WO2007/016735<br />
(51) IPC2011.01:E04C3/07; E04G5/00; F16S3/02,06; A47B55/00; A47B47/<br />
02; A47B96/14; B65G1/02<br />
(71) Dematic Pty Ltd<br />
(72) Clarke, Murray; Berry, Paul; Celati, Stephen;<br />
(31) 05 904257 (32) 8 Aug 2005 (33) AU<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) Disclosed is a storage rack beam (10) which includes top (12) and<br />
bottom (13) flanges and at least one web (14) that interconnects the<br />
flanges (12, 13). The web (14) includes at least one stiffening formation<br />
(16) arranged to stiffen an intermediate region <strong>of</strong> the web (14) along a<br />
substantial portion <strong>of</strong> its length so as to resist lateral impact loading applied<br />
to the beam (10). The beam (10) may take various forms, including<br />
first and second U-shaped sections in opposed abutting relationship, or<br />
formed as a closed S-shaped pr<strong>of</strong>ile. The application also discloses a<br />
storage rack beam that has a vertical loading capacity and a horizontal<br />
loading capacity, where at least part <strong>of</strong> the horizontal loading capacity is<br />
independent <strong>of</strong> the vertical loading capacity applied to the beam.<br />
(21) 565910 (22) 1 Aug 2006<br />
(54) Optimizing the detection <strong>of</strong> tollable vehicles on toll roads<br />
(86) PCT/EP2006/064901 (87) WO2007/025826<br />
(51) IPC2011.01:G07B15/00; G08G1/017<br />
(71) SIEMENS AKTIENGESELLSCHAFT<br />
(72) Petroczi, Julius;<br />
(31) 05 041068 (32) 30 Aug 2005 (33) DE<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed is a method for optimizing the detection <strong>of</strong> vehicles liable to<br />
pay tolls on toll roads <strong>of</strong> a road network. The method includes using a<br />
vehicle-mounted position determining unit connected to a vehicle external<br />
management unit. Toll roads are overlaid in an electronic image <strong>of</strong><br />
the road network by detection zones (E), and the position determining<br />
unit, upon determining vehicle positions (PE) within the detection zones,<br />
determines toll-related data and sends the data to the management unit.<br />
Monitoring zones (K) are also provided in the image, and are assigned to<br />
and extend beyond their assigned detection zone. The position determining<br />
unit, upon determining journeys exclusively within the monitoring<br />
zone and outside the detection zone, sends position data (P-K-) <strong>of</strong> the<br />
journeys to the management unit. The management unit then performs a<br />
retrospective check <strong>of</strong> the position data (PK-) to determine whether the<br />
detection zone should be adjusted, and adjusts if necessary.<br />
(21) 565981 (22) 29 Aug 2006<br />
(54) Octagonal bulk bin constructed from a single blank with self-locking<br />
webbed bottom flats<br />
(86) PCT/US2006/033950 (87) WO2007/027836<br />
(51) IPC2011.01:B65D5/02,06,10,42<br />
(71) International Paper Company<br />
(72) Wisecarver, Mark; Quaintance, Benjamin;<br />
(31) 05 712236 (32) 29 Aug 2005 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) An octagonal bulk bin (10) erected from a blank is disclosed. The bin<br />
(10) has sidewalls (11, 12), end walls (13, 14) and diagonal corner panels<br />
(15, 16, 17, 18) interposed between adjacent sidewalls and end walls.<br />
Major bottom flaps (22, 23) are joined to a bottom edge <strong>of</strong> the sidewalls.<br />
Bottom flaps are joined to the bottom edge <strong>of</strong> the walls and panels that<br />
inter connect to form the bottom <strong>of</strong> the bin (10). Anti-tear cuts are formed<br />
in the bottom flaps joined to the sidewalls (11, 12) and foldable web panels<br />
interconnect opposite edges <strong>of</strong> bottom the flaps joined to the end<br />
walls (13, 14).<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 95 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(21) 566004 (22) 29 Aug 2006<br />
(54) Indoor unit <strong>of</strong> air conditioner<br />
(86) PCT/JP2006/316998 (87) WO2007/026706<br />
(51) IPC2011.01:F24F13/28; B01D46/10; F24F13/00; F24F1/00; B01D46/<br />
00<br />
(71) Toshiba Carrier Corporation<br />
(72) Ozawa, Tetsuro; Suzuki, Hideto; Sano, Mitsukuni; Mishima, Takechika;<br />
Okada, Kaku; Takeya, Nobuyuki; Hida, Yoshiyuki; Shibayama, Yoshiyuki;<br />
(31) 05 249735 (32) 30 Aug 2005 (33) JP<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) An indoor machine <strong>of</strong> an air conditioner, comprising a front air filter<br />
(5A) and an upper air filter (5B) installed to face a front suction port (4)<br />
and an upper suction port (6), a front suction frame (7A) holdingly supporting<br />
the front air filter (5A) movably in the direction <strong>of</strong> the upper suction<br />
port (6), an upper suction frame (7B) holdingly supporting the upper<br />
air filter (5B) movably in the direction <strong>of</strong> the front suction port (4), a front<br />
moving mechanism reciprocatingly moving the front air filter (5A), an<br />
upper moving mechanism reciprocatingly moving the upper air filter (5B),<br />
and a cleaning unit (Z) having a rotary brush removing dust from the<br />
front air filter (5A) and the upper air filter (5B) and a dust collection part<br />
collecting the dust. The front moving mechanism and the upper moving<br />
mechanism alternately move the front air filter (5A) and the upper air<br />
filter (5B) to the cleaning unit (Z) for cleaning.<br />
(21) 566012 (22) 31 Jul 2006<br />
(54) Quinoline derivatives as antibacterial agents<br />
(86) PCT/EP2006/064847 (87) WO2007/014934<br />
(51) IPC2011.01:A61K31/4709; A61P31/04; C07D413/06<br />
(71) Janssen Pharmaceutica N.V.<br />
(72) Andries, Koenraad Jozef Lodewijk Marcel; Koul, Anil; Guillemont,<br />
Jerome Emile Georges; Pasquier, Elisabeth Therese Jeanne;<br />
(31) 05 05107155 (32) 3 Aug 2005 (33) EP<br />
(74) BALDWINS INTELLECTUAL PROPERTY, Level 14, Baldwins Centre,<br />
342 Lambton Quay, Wellington 6011, New Zealand<br />
(57) Disclosed is the use <strong>of</strong> quinoline derivatives <strong>of</strong> formula (Ia) or (Ib) for<br />
the manufacture <strong>of</strong> a medicament for the treatment <strong>of</strong> a bacterial infection,<br />
wherein the substituents are defined within the specification, and<br />
provided that the bacterial infection is other than a Mycobacterial infection.<br />
Other quinoline derivatives which comprise a naphthalene group<br />
are also disclosed. The use <strong>of</strong> these derivatives in combination with other<br />
antibacterial agents, for the manufacture <strong>of</strong> a medicament for the treatment<br />
<strong>of</strong> a bacterial infection other than a Mycobacterial infection is also<br />
disclosed.<br />
(21) 566065 (22) 17 Jul 2006<br />
(54) Shin guard with bandage forming opening for calf muscle, and shield<br />
attached to bandage<br />
(86) PCT/EP2006/007005 (87) WO2007/014641<br />
(51) IPC2011.01:A63B71/12; A41D13/00,015; A41D31/00<br />
(71) SCHEFFER, Harald<br />
(72) Scheffer, Harald;<br />
(31) 05 036170 (32) 2 Aug 2005 (33) DE<br />
(74) McCABE & COMPANY, Level 6, Polo House, 267 Wakefield Street,<br />
Wellington, New Zealand<br />
(57) A shin pad in particular for footballers, comprises a rigid shield element<br />
3 which is to be positioned in front <strong>of</strong> the user's shin, and attach-<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 96 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
ments for fastening the shield element on the user's lower leg 1, where<br />
the fastening attachments have a bandage 2 which at least partially surrounds<br />
the user's lower leg 1, and the shield element 3 has a detachable<br />
connection with the bandage 2 over a considerable part <strong>of</strong> its inner surface,<br />
which faces the user's shin, such that the forces acting on the<br />
shield element are distributed over the shield element such that the static<br />
frictional force between the bandage and the lower leg is not exceeded.<br />
The bandage 2 has an opening 5 which leaves the user's calf 4 free, so<br />
that the connection areas 6, 7 remain above and below the opening 5<br />
and at least partially surround the user's lower leg 1. The connection<br />
areas 6, 7 are positioned so near to the hollow <strong>of</strong> the user's knee and<br />
ankle, and are <strong>of</strong> such a length, that they do not impede activity <strong>of</strong> the<br />
user's calf muscle.<br />
(21) 566151 (22) 13 Sep 2006<br />
(54) Dispenser having a reservoir comprising a porous material<br />
(86) PCT/US2006/035368 (87) WO2007/033107<br />
(51) IPC2011.01:A01K11/00; A01K13/00; A01K27/00<br />
(71) Aircom Manufacturing, Inc.<br />
(72) Trompen, Mick A; Lyon, Gregory A; Meyer, Jeffery A;<br />
(31) 05 226478 (32) 14 Sep 2005 (33) US<br />
(74) Shelston IP, Level 21, 60 Margaret Street, Sydney, NSW 2000, Australia<br />
(57) A dispenser is disclosed. The dispenser comprises a shell having an<br />
opening; means for attaching the dispenser to an animal; a reservoir<br />
disposed in the shell comprising a porous material containing a liquid<br />
substance; and a wick having a first portion in direct contact with the<br />
porous material and a second portion positioned adjacent the opening.<br />
The wick is in fluid communication with the reservoir. The wick has a<br />
greater capillary attraction than the reservoir whereby during use <strong>of</strong> the<br />
dispenser the wick draws the liquid substance from the reservoir through<br />
the first portion <strong>of</strong> the wick and the second portion <strong>of</strong> the wick deposits<br />
the liquid substance on an animal upon contact. Substantially all payout<br />
<strong>of</strong> the liquid substance from the reservoir is delivered by wicking action<br />
<strong>of</strong> the wick and through the opening.<br />
(21) 566392 (22) 28 Aug 2006<br />
(54) Motion capture using primary and secondary markers<br />
(86) PCT/US2006/033715 (87) WO2007/025301<br />
(51) IPC2011.01:G06T7/20<br />
(71) SONY CORPORATION; SONY PICTURES ENTERTAINMENT INC.<br />
(72) Gordon, Demian; Hauck, Dennis J;<br />
(31) 05 711923 (32) 26 Aug 2005 (33) US<br />
(31) 05 711905 (32) 26 Aug 2005 (33) US<br />
(31) 06 467494 (32) 25 Aug 2006 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) A system and a method for capturing the motion <strong>of</strong> a plurality <strong>of</strong> primary<br />
markers and at least one secondary marker are disclosed. The<br />
system comprises an apparatus, a plurality <strong>of</strong> primary markers coupled<br />
to a target and at least one secondary marker coupled to the target.<br />
The apparatus comprises means for capturing a plurality <strong>of</strong> primary marker<br />
data points by illuminating the plurality <strong>of</strong> primary markers; and capturing<br />
a response <strong>of</strong> the plurality <strong>of</strong> primary markers to the illumination. The<br />
plurality <strong>of</strong> primary markers includes a plurality <strong>of</strong> reflective markers, and<br />
the response includes a reflection <strong>of</strong> the illumination by the plurality <strong>of</strong><br />
reflective markers. Each primary marker data point <strong>of</strong> the plurality <strong>of</strong><br />
primary marker data points corresponds to one primary marker <strong>of</strong> the<br />
plurality <strong>of</strong> primary markers. The illumination is subject to periodic gating<br />
to generate on-states and <strong>of</strong>f-states <strong>of</strong> the illumination and the reflection<br />
<strong>of</strong> the illumination is captured during an on-state <strong>of</strong> the illumination.<br />
The apparatus also comprises means for capturing at least one secondary<br />
marker signature, each secondary marker signature corresponding<br />
to and uniquely identifying each secondary marker <strong>of</strong> the at least one<br />
secondary marker. The at least one secondary marker signature is captured<br />
by capturing a unique attribute <strong>of</strong> the at least one secondary marker<br />
during an <strong>of</strong>f-state <strong>of</strong> the illumination.<br />
The apparatus also comprises means for identifying the plurality <strong>of</strong> primary<br />
markers using the at least one secondary marker signature.<br />
The means for capturing a plurality <strong>of</strong> primary marker data points and the<br />
means for capturing at least one secondary marker signature comprise<br />
an image capture module configured to capture a plurality <strong>of</strong> primary<br />
marker data points and each primary marker data point corresponds to<br />
one primary marker <strong>of</strong> the plurality <strong>of</strong> primary markers. The image capture<br />
module also is configured to capture at least one secondary marker<br />
signature. The means for identifying the plurality <strong>of</strong> primary markers using<br />
the at least one secondary marker signature comprises a primary<br />
marker tracking module configured to identify the plurality <strong>of</strong> primary<br />
markers using the at least one secondary marker signature.<br />
(21) 566435 (22) 23 Oct 2006<br />
(54) A flexible knitting pin<br />
(86) PCT/IN2006/000417 (87) WO2007/049300<br />
(51) IPC2011.01:D04B3/02<br />
(71) T.A. Devagnanam<br />
(72) Devagnanam, T.A.;<br />
(31) 05 CH 1571 (32) 28 Oct 2005 (33) IN<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 97 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(74) Shelston IP, Level 21, 60 Margaret Street, Sydney, NSW 2000, Australia<br />
(57) A flexible knitting pin and a process for manufacturing the flexible<br />
knitting pin is disclosed. The knitting pin includes two relatively stiff shanks<br />
having first and second ends, where each shank is pointed at the first<br />
end and has a ferrule which holds a ball head screw at the second end.<br />
The second ends <strong>of</strong> the shanks are connected with each other by a<br />
flexible hollow connecting material comprising a joint. A brass adapter<br />
connects each shank with the flexible hollow connecting material for<br />
smooth transition.<br />
(21) 566437 (22) 12 Oct 2006<br />
(54) Cam tube bracket with tab pair engaging cam tube outer surface<br />
(86) PCT/US2006/040244 (87) WO2007/044928<br />
(51) IPC2011.01:F16D65/22,16,14<br />
(71) Hendrickson International Corporation<br />
(72) Pierce, Phillippi R; White, Jay D; Morris, Jeff; Gregg, Dane;<br />
(31) 05 725933 (32) 12 Oct 2005 (33) US<br />
(74) FISHER ADAMS KELLY, Level 29, 12 Creek Street, Brisbane, Queensland<br />
4000, Australia<br />
(57) A cam shaft support/enclosure assembly for brake systems <strong>of</strong> heavyduty<br />
vehicles is mounted on a beam <strong>of</strong> an axle/suspension system and<br />
includes a cam tube (54') . A bracket for mounting the cam tube on the<br />
beam includes a pair <strong>of</strong> plates (82,84) that are mounted on the beam.<br />
Each one <strong>of</strong> the plates is formed with an opening for receiving the cam<br />
tube (54') and includes at least three tabs (90) , and preferably four tabs,<br />
that extend outwardly from each respective plate adjacent the opening<br />
and contact the outer surface <strong>of</strong> the cam tube (54') . Each tab includes a<br />
generally arched and optionally textured face for mating with an outer<br />
surface <strong>of</strong> the cam tube, which may also be optionally textured, so that<br />
when the plates are mounted the tabs engage the cam tube in a presstype<br />
fit, minimizing movement <strong>of</strong> the cam tube.<br />
(21) 566630 (22) 1 Aug 2006<br />
(54) A water heater where the flue and flue outlet pipe have a length relationship<br />
to control combustion <strong>of</strong> the pilot<br />
(86) PCT/AU2006/001085 (87) WO2007/030855<br />
(51) IPC2011.01:F24H9/18; F24D17/00; F24H1/24; F23J11/00; F23D14/<br />
26<br />
(71) Dux Manufacturing Limited<br />
(72) Pussell, Patrick;<br />
(31) 05 905137 (32) 16 Sep 2005 (33) AU<br />
(74) SPRUSON & FERGUSON, St Martins Tower, Level 35, 31 Market<br />
Street, Sydney, New South Wales 2000, Australia<br />
(57) A water heater (10) with flue proportions that control the combustion<br />
<strong>of</strong> the pilot light. The heater (10) has a tank (12), a burner (26) and a<br />
heated gas outlet duct (40). The tank (12) has a central flue (14) with an<br />
outlet (24) at the top (20) <strong>of</strong> the tank (12). The tank (12) in use is mounted<br />
with the flue (14) vertically. The burner (26) is located beneath the tank<br />
(12) and has an air inlet (32) and a pilot flame and is adapted to a burn a<br />
fuel to discharge heated gases up through the flue (14). The heated gas<br />
outlet duct (40) is <strong>of</strong> substantially unrestricted cross-section and has an<br />
upper, first end (42) in gas communication with the flue outlet (24) and a<br />
second, lower end (46) in gas communication with atmosphere. When<br />
only the pilot flame is burning, the heated gas outlet duct (40) is adapted<br />
to restrict the air drawn into the flue (14) via the air inlet (32) to the minimum<br />
amount required to maintain the pilot flame alight. This is achieved<br />
by the duct (40) having approximately the same cross sectional area <strong>of</strong><br />
the flue (14) and having approximately 25% <strong>of</strong> the length <strong>of</strong> the flue (14)<br />
i.e. L2 = L1 x ~0.25.<br />
(21) 566756 (22) 22 Sep 2006<br />
(54) Safety needle assembly with spring axis spaced from needle assembly<br />
axis<br />
(86) PCT/US2006/037288 (87) WO2007/035924<br />
(51) IPC2011.01:A61M5/00; A61M25/06<br />
(71) TYCO HEALTHCARE GROUP LP<br />
(72) Jones, Scott; Clark, George;<br />
(31) 05 719762 (32) 22 Sep 2005 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) A needle safety device is provided having a housing, a needle assembly<br />
movably mounted within the housing and a spring for biasing the<br />
needle assembly within the housing. The needle assembly is movable<br />
along a first axis and the spring is movable along the second axis different<br />
from the first. There is also provided a lens for enhancing visualization<br />
<strong>of</strong> the flow <strong>of</strong> fluid through the needle safety device. There is further<br />
provided a safety sheath for covering a needle <strong>of</strong> the needle assembly<br />
and restraining the needle assembly against movement due to the bias<br />
<strong>of</strong> the spring.<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 98 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(21) 566780 (22) 29 Jun 2006<br />
(54) Thermal energy system with solar collection and controller to predict<br />
operation and change flow rate<br />
(86) PCT/GB2006/002408 (87) WO2007/028938<br />
(51) IPC2011.01:F24D11/02; F24D19/10; F24J2/04,24<br />
(71) Endoenergy Systems Ltd<br />
(72) Virk, Gurvinder Singh;<br />
(31) 05 0518218 (32) 7 Sep 2005 (33) GB<br />
(74) JAMES & WELLS, Level 12, KPMG Centre, 85 Alexandra Street,<br />
Hamilton, New Zealand<br />
(57) Disclosed is a thermal energy system (3) for heating and/or cooling<br />
applications. The system has: solar collection means (10) for transferring<br />
heat energy to and/or from a heat transfer fluid; thermal upgrading<br />
means (44) for increasing the thermal energy within the system; and<br />
thermal storage means (48, 50). The collection means, upgrading means<br />
and storage means are connected so as to allow the transfer <strong>of</strong> heat<br />
there between via the heat transfer fluid. Control means are arranged to<br />
receive readings <strong>of</strong> operational variables from the thermal energy system<br />
and to process the operational variables using a system model so<br />
as to predict future operational variables for the system. The control means<br />
controls the flow <strong>of</strong> the heat transfer fluid around the system based on<br />
the predicted operational variables. The flow is controlled by controlling<br />
<strong>of</strong> operation <strong>of</strong> one or more pumps (36, 62, 70, 78, 80) or fans and one or<br />
more valves (40, 42, 54, 86), the valves being disposed between the<br />
solar collection means and the thermal storage means.<br />
(21) 566816 (22) 6 Oct 2006<br />
(54) Dispensing <strong>of</strong> restricted goods from an authorised vendor to an approved<br />
purchaser<br />
(86) PCT/AU2006/001458 (87) WO2007/041767<br />
(51) IPC2011.01:G07F7/08; G06Q50/00; G06Q90/00<br />
(71) Bluepoint International Pty Ltd<br />
(72) Allinson, John Clive; Boyd, Garry David;<br />
(31) 05 905515 (32) 7 Oct 2005 (33) AU<br />
(74) I P Strategies, 24 Christowel Street, Camberwell, Victoria 3124, Australia<br />
(57) A dispenser and a method <strong>of</strong> dispensing restricted goods by an authorized<br />
vendor to an approved purchaser is disclosed. The dispenser<br />
comprises: a cabinet containing an inventory storage system, a purchaser<br />
transaction module, a reject system and a control system where the inventory<br />
storage system includes product storage in rows and columns.<br />
The purchaser transaction module includes an audio communication link<br />
from the dispenser to the authorized vendor. A payment transaction system<br />
in the dispenser verifies payment for the product and a collection<br />
tray in the dispenser is locked until the vendor releases the product to<br />
the purchaser. The reject system securely removes product to a reject<br />
hopper at any time after the product is held by the product selection<br />
device but prior to the vendor releasing the product from the collection<br />
tray. The control system includes an identification device and a product<br />
selection device where the identification device enables the vendor to<br />
verify the purchaser's status as an approved purchaser. The product<br />
selection device enables verification that the product selected is correct<br />
and holds and carries the product from its storage location to one or<br />
more <strong>of</strong> a printing location, viewing location, and issue tray all located<br />
within the dispenser. A reject key enables the vendor to actuate the reject<br />
system and a release key unlocks the collection tray.<br />
(21) 566881 (22) 21 Sep 2006<br />
(54) Cover for a vent<br />
(86) PCT/AU2006/001386 (87) WO2007/033423<br />
(51) IPC2011.01:F24F13/28,06,068<br />
(71) Mariella Elizabeth Niveagh Rosso<br />
(72) Rosso, Mariella Elizabeth Niveagh;<br />
(31) 2005905215 (32) 21 Sep 2005 (33) AU<br />
(74) DAVIES COLLISON CAVE - MELBOURNE, 1 Nicholson Street, Melbourne,<br />
Victoria, Australia<br />
(57) Disclosed is a cover for a vent <strong>of</strong> a ducted air system. The cover<br />
includes a filter for inhibiting traffic <strong>of</strong> particulate matter through said vent<br />
and a fastener for securing the cover around a portion <strong>of</strong> the vent shaped<br />
for insertion into a corresponding outlet <strong>of</strong> the ducted air system. The<br />
filter has a hollow receptacle that extends beyond the portion <strong>of</strong> the vent<br />
shaped for insertion into the outlet. The receptacle is shaped to accommodate<br />
a vent closure which is operable to move between open and<br />
closed conditions. When in an open condition the vent closure extends<br />
beyond the portion <strong>of</strong> the vent shaped for insertion into the corresponding<br />
outlet <strong>of</strong> the ducted air system.<br />
(21) 567102 (22) 2 Oct 2006<br />
(54) Optical device for led light sources<br />
(86) PCT/CH2006/000535 (87) WO2007/036064<br />
(51) IPC2011.01:G02B6/00,42<br />
(71) Radical Form Lighting Ltd.<br />
(72) Zweig, Frederic; Buhrer, Thomas;<br />
(31) 05 1581 (32) 30 Sep 2005 (33) CH<br />
(74) Shelston IP, Level 21, 60 Margaret Street, Sydney, NSW 2000, Australia<br />
(57) Disclosed is an optical device for the targeted reproduction <strong>of</strong> light<br />
emitted by LED light sources (6). The optical device comprises at least<br />
two component parts, a first optical component part (10) in the form <strong>of</strong> a<br />
solid waveguide and another component part for connection to the LED<br />
light source. In a system <strong>of</strong> Cartesian co-ordinates, the first optical component<br />
part (10) has a length in the y direction shorter than or equal to its<br />
length in the z direction and shorter than or equal to its length in the x<br />
direction. The first part comprises: first and second planar outer surfaces<br />
opposing in the x-z plane; third and fourth planar or nonplanar outer surfaces<br />
substantially opposing on the x-y plane; and fifth and sixth opposing<br />
outer surfaces curved in a convex manner with regard to the y-z<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 99 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
plane. The third and fourth outer surfaces are square, and the fifth and<br />
sixth outer surfaces are curved such that the fourth outer surface has a<br />
length in the x·direction that is smaller than the length <strong>of</strong> the third outer<br />
surface.<br />
(21) 567195 (22) 12 Oct 2006<br />
(54) Method <strong>of</strong> operating a plurality <strong>of</strong> clean rooms<br />
(86) PCT/US2006/040068 (87) WO2007/050320<br />
(51) IPC2011.01:F24F3/16; F24F11/00<br />
(71) Charles W Spengler<br />
(72) Spengler, Charles W;<br />
(31) 05 258057 (32) 26 Oct 2005 (33) US<br />
(74) PIPERS, Level 1, 5A Pacific Rise, Mt Wellington, Auckland, New Zealand<br />
(57) A method <strong>of</strong> operating a plurality <strong>of</strong> clean rooms in a compound within<br />
a common area <strong>of</strong> an enclosed building is disclosed. Each clean room<br />
consists <strong>of</strong> a portable enclosure including a generally rectangular open<br />
frame covered on its top wall and sidewalls by a flexible, substantially air<br />
impermeable sheet material. Air supply blower means outside <strong>of</strong> and<br />
connected to the clean room provides filtered air into the room. An entrance<br />
means through a sidewall provides access to the clean room. The<br />
method comprises: (a) arranging the clean rooms in the compound consisting<br />
<strong>of</strong> two parallel spaced rows <strong>of</strong> clean rooms with an access corridor<br />
there between and with the entrances to the clean rooms <strong>of</strong> each row<br />
opening into the access corridor; (b) providing a plurality <strong>of</strong> blowers<br />
operably connected to each clean room for supplying clean filtered air<br />
into the respective clean rooms, and permitting air to escape from the<br />
clean room beneath the sidewalls there<strong>of</strong>; (c) continuously operating the<br />
blowers to produce a clean air bubble consisting <strong>of</strong> a volume <strong>of</strong> air containing<br />
at least about 75% recirculated filtered air which has escaped<br />
from the clean rooms, and (d) arranging the clean rooms and the blowers<br />
in a pattern wherein the clean air bubble created by each blower<br />
overlaps the clean air bubble produced by at least two other blowers,<br />
whereby the entire compound <strong>of</strong> clean rooms is contained within the<br />
overlapping bubbles produced by the blowers.<br />
(21) 567232 (22) 10 Aug 2006<br />
(54) Body massager with a light source mounted on a massage formation<br />
(86) PCT/US2006/031051 (87) WO2007/032835<br />
(51) IPC2011.01:A61H7/00<br />
(71) FKA DISTRIBUTING CO. D/B/A HOMEDICS, INC.<br />
(72) Ferber, Roman; Wei, Huang Wen;<br />
(31) 05 223685 (32) 9 Sep 2005 (33) US<br />
(74) PIPERS, Level 1, 5A Pacific Rise, Mt Wellington, Auckland, New Zealand<br />
(57) Disclosed is a massage apparatus with illumination effects. The apparatus<br />
includes a housing (46); a massage formation (136’) provided<br />
on the housing for contacting a body part <strong>of</strong> a user; a massage mechanism<br />
oriented within the housing for imparting a massage effect to the<br />
massage formation for massaging the body part; and a light source (146)<br />
provided on the massage formation for conveying an illumination effect<br />
from the massage formation. The apparatus further includes: a carriage<br />
(52) oriented in the housing for limited translation in the housing, the<br />
massage formation provided on the carriage; a motor supported upon<br />
the carriage; and a shaft (110) mounted on the carriage and operably<br />
driven by the motor for rotation about an axis. The shaft has a pair <strong>of</strong><br />
secondary shaft portions each canted relative to the shaft axis. The ap-<br />
paratus also has: a pair <strong>of</strong> massage brackets (124) each joumalled to<br />
one <strong>of</strong> the secondary shaft portions and engaging the carriage for limited<br />
rotation about the shaft axis such that rotation <strong>of</strong> the shaft oscillates the<br />
massage brackets relative to the carriage; a pair <strong>of</strong> massage arms (136’)<br />
each pivotally connected to one <strong>of</strong> the massage brackets; and a pair <strong>of</strong><br />
massage rollers (138’, 140’) each pivotally connected to one <strong>of</strong> the massage<br />
arms. The massage rollers impart a rolling massage effect upon a<br />
desired body part <strong>of</strong> the user as the carriage is translated relative to the<br />
housing and for imparts a kneading massage effect upon the portion <strong>of</strong><br />
the user's body as the massage brackets oscillate relative to the carriage.<br />
(21) 567257 (22) 20 Oct 2006<br />
(54) Method <strong>of</strong> cracking a crude product to produce additional crude products<br />
(86) PCT/US2006/040991 (87) WO2007/050450<br />
(51) IPC2011.01:C10G1/00,02; C10G11/00<br />
(71) SHELL INTERNATIONALE RESEARCH MAATSCHAPPIJ B.V.<br />
(72) Mo, Weijian; Nair, Vijay; Roes, Augustinus Wilhelmus Maria;<br />
(31) 05 729763 (32) 24 Oct 2005 (33) US<br />
(31) 06 794298 (32) 21 Apr 2006 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed is a method for producing a crude product, comprising:<br />
producing formation fluid from a subsurface in situ pyrolysis heat treatment<br />
process; separating the formation fluid to produce a liquid stream<br />
and a first gas stream, wherein the first gas stream comprises olefins;<br />
fractionating the liquid stream to produce one or more crude products,<br />
wherein at least one <strong>of</strong> the crude products has a boiling range distribution<br />
from 38 degrees Celsius and 343 degrees Celsius as determined by<br />
ASTM Method D5307; and catalytically cracking the crude product having<br />
the boiling range distribution from 38 degrees Celsius and 343 degrees<br />
Celsius by a fluidizable cracking catalyst comprising a molecular<br />
sieve having cracking activity dispersed in a porous, inorganic refractory<br />
oxide matrix or binder to produce one or more additional crude products<br />
comprising gasoline hydrocarbons having an octane number <strong>of</strong> at least<br />
70, wherein at least one <strong>of</strong> the additional crude products is a second gas<br />
stream, and the second gas stream has a boiling point <strong>of</strong> at most 38<br />
degrees Celsius at 0.101 Mpa and comprises hydrocarbons having a<br />
carbon number <strong>of</strong> at least 3. Also disclosed the product obtained by said<br />
method.<br />
(21) 567376 (22) 27 Oct 2006<br />
(54) Single or multiple stage blower and nested volute(s) and/or impeller(s)<br />
therefor<br />
(86) PCT/AU2006/001617 (87) WO2007/048206<br />
(51) IPC2011.01:A61M16/00; A61M1/00; F04B17/00; F04D29/60,66<br />
(71) ResMed Limited<br />
(72) Kenyon, Barton John; Reed, Nicholas Jerome; Wilson, Andrew; Smith,<br />
Ian Malcolm;<br />
(31) 05 730875 (32) 28 Oct 2005 (33) US<br />
(31) 06 775333 (32) 22 Feb 2006 (33) US<br />
(31) 06 841202 (32) 31 Aug 2006 (33) US<br />
(74) JAMES & WELLS, Level 12, KPMG Centre, 85 Alexandra Street,<br />
Hamilton, New Zealand<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 100 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(57) A single ended or double-ended blower comprising a blower motor<br />
assembly supporting opposed first (258) and second (260) shaft ends,<br />
the first (258) and second (260) shaft ends having respective first (244)<br />
and second (248) impellers attached thereto and enclosed within first<br />
(247) and second (251) volutes, respectively, wherein the first volute<br />
(247) is connected to an inlet (264) and the second volute (251) is connected<br />
to an outlet (276); and the blower motor assembly supported in a<br />
chassis enclosure; a radially outer inter-stage path between the first (247)<br />
and second (251) volute, wherein the second (251) volute is at least<br />
partially substantially concentrically nested with the radially outer interstage<br />
gas path.<br />
Divisional filed as 590498<br />
(21) 567401 (22) 11 Oct 2006<br />
(54) Ear tag for the identification <strong>of</strong> an animal, comprising a deformable<br />
element for accomodating a pin<br />
(86) PCT/EP2006/067264 (87) WO2007/042528<br />
(51) IPC2011.01:A01K11/00; G09F3/00<br />
(71) Allflex Europe SAS<br />
(72) Costantini, Anne; Hilpert, Jean-Jacques;<br />
(31) 0510448 (32) 13 Oct 2005 (33) FR<br />
(74) ELLIS TERRY, Level 12, 45 Johnston Street, Wellington 6011, New<br />
Zealand<br />
(57) An ear tag for the identification and tagging <strong>of</strong> animals is disclosed.<br />
The ear tag combines a receiving button and a pin by irreversible interlocking<br />
<strong>of</strong> the receiving button and pin. The button comprises a head<br />
inside <strong>of</strong> which is located a cavity for axial accommodation <strong>of</strong> a punch <strong>of</strong><br />
the pin. The head is secured to a shell for holding the punch where the<br />
shell is equipped with an opening for inserting the punch inside the button<br />
toward the cavity. A holding shoulder holds the punch against the<br />
withdrawal <strong>of</strong> the punch from the button by stopping a shoulder that the<br />
punch comprises against the holding shoulder. An axial wall <strong>of</strong> the holding<br />
shell that delimits the opening is formed <strong>of</strong> an elastic material and is<br />
radially deformable to allow passage <strong>of</strong> the punch through the opening.<br />
At least one chamber is located between the head and the axial wall for<br />
the accommodation <strong>of</strong> the axial wall that is deformed under the action <strong>of</strong><br />
the passage <strong>of</strong> the punch through the opening.<br />
(21) 567507 (22) 17 Oct 2006<br />
(54) Food holding cabinet with removable tray covers<br />
(86) PCT/US2006/040411 (87) WO2007/047597<br />
(51) IPC2011.01:A47J36/34; F24C15/16<br />
(71) MERCO/SAVORY LLC<br />
(72) Jones, Douglas S;<br />
(31) 05 727343 (32) 17 Oct 2005 (33) US<br />
(74) HENRY HUGHES, 119-125 Willis Street, Wellington, New Zealand<br />
(57) A food holding cabinet having a housing defining a heating chamber<br />
for holding a covered food tray in a tray location has a pair <strong>of</strong> elongated<br />
rigid rods mounted to the housing for suspending a food tray cover thereon<br />
in a position above the tray location. A front rod extends across the opening<br />
to the heating chamber and supports the front end <strong>of</strong> the tray cover<br />
and a rear rod supports the rear <strong>of</strong> the cover. When a food tray is inserted<br />
into the tray location, it lifts and supports the cover. When the tray<br />
is removed, the front rod prevents removal <strong>of</strong> the cover along with the<br />
underlying tray. The front rod is spring-loaded to be pulled away from the<br />
housing to facilitate removal <strong>of</strong> the cover. A tray cover is also provided.<br />
Divisional filed as 590721<br />
(21) 567538 (22) 19 Oct 2006<br />
(54) A slip type pipe joint<br />
(86) PCT/AU2006/001547 (87) WO2007/045033<br />
(51) IPC2011.01:F16L25/12; F16L27/12; F16L47/10<br />
(71) JTL Australia Pty Ltd<br />
(72) Phillipps, Guy Malcolm;<br />
(31) 05 905769 (32) 19 Oct 2005 (33) AU<br />
(74) JAMES & WELLS, Level 12, KPMG Centre, 85 Alexandra Street,<br />
Hamilton, New Zealand<br />
(57) A slip type pipe fitting for joining two spaced apart plastic pipe ends is<br />
disclosed. The fitting includes: a first insert (12) having an elongate pipe<br />
support portion (14), insertable into an internal bore <strong>of</strong> a first plastic pipe<br />
end (11), and a distal end (16) in use projecting outside the first pipe end<br />
(11) and having a first annular seal (17); an elongate hollow pipe connector<br />
(30) defining a bore (32) and having first and second connector ends,<br />
the inner bore (32) receiving the distal end (16) and first annular seal (17)<br />
<strong>of</strong> the first insert (12) for sliding movement and sealing therein; and a<br />
first compression joining assembly including a first end nut (42) for mechanically<br />
joining the first connector end (40) to the first pipe end (11) by<br />
a compression action sandwiching the first pipe end (11) between the<br />
first end annular member (42) and the pipe support portion (14) thereby<br />
locking the connector (30) with respect to the first pipe end (11). In use<br />
the support portion (14) extends into the first pipe end (11) an axial distance<br />
AL such that said locking can occur over a range <strong>of</strong> axial positions.<br />
(21) 567570 (22) 12 Oct 2006<br />
(54) Biphenyl derivatives as modulators <strong>of</strong> voltage gated ion channels<br />
(86) PCT/US2006/040156 (87) WO2007/047474<br />
(51) IPC2011.01:C07D275/02; A61K31/425; C07D417/10<br />
(71) Vertex Pharmaceuticals Incorporated<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 101 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
(72) Martinborough, Esther; Lehsten, Danielle; Neubert, Timothy; Kawatkar,<br />
Aarti Sameer; Zimmermann, Nicole; Termin, Andreas;<br />
(31) 05 725686 (32) 12 Oct 2005 (33) US<br />
(74) CULLEN & CO, Level 32, 239 George Street, Brisbane, QLD 4001,<br />
Australia<br />
(57) Disclosed is a biphenyl sulfamoyl compound <strong>of</strong> formula I: or a<br />
pharmaceutically acceptable salt there<strong>of</strong> wherein: ring Z is a 5 membered<br />
ring having at least one ring heteroatom selected from O, S, N, and NH,<br />
z is 0 to 4; Q is a bond or is a alkylidine chain, or a spirocycloalkylene<br />
moeity; RQ is a aliphatic group, a monocyclic ring or a bicyclic ring system,<br />
RN and RM and Y are defined in the specification. Also disclosed is<br />
a composition comprising said compound, a method <strong>of</strong> inhibiting one or<br />
more <strong>of</strong> NaV1.1, NaV1.2, NaV1.3, NaV1.4, NaV1.5, NaV1.6, NaV1.7,<br />
NaV1.8, NaV1.9, or CaV2.2 activity in a biological sample comprising<br />
contacting said biological sample with said compound and the use <strong>of</strong><br />
said compound in the manufacture <strong>of</strong> a medicament to treat a disease,<br />
disorder, or condition selected from acute, chronic, neuropathic, or inflammatory<br />
pain, arthritis, migraine, cluster headaches, trigeminal neuralgia,<br />
herpetic neuralgia, general neuralgias, epilepsy or epileptic conditions,<br />
neurodegenerative disorders, psychiatric disorders such as anxiety<br />
and depression, myotonia, arrhythmia, movement disorders, neuroendocrine<br />
disorders, ataxia, multiple sclerosis, irritable bowel syndrome,<br />
incontinence, visceral pain, osteoarthritis pain, postherpetic neuralgia,<br />
diabetic neuropathy, radicular pain, sciatica, back pain, head or neck<br />
pain, severe or intractable pain, nociceptive pain, breakthrough pain,<br />
postsurgical pain, stroke, bipolar disorders, and cancer pain.<br />
(21) 567733 (22) 26 Oct 2005<br />
(54) Upright shaft post capable <strong>of</strong> accommodating various containers<br />
(86) PCT/US2005/039397 (87) WO2007/067161<br />
(51) IPC2011.01:A47F3/14; A47G29/02; B25H3/02; A44B11/08,26;<br />
A47B49/00; A47F5/05<br />
(71) Steelworks Hardware, LLC<br />
(72) Nguy, Chanwa; Lin, Pei Ying;<br />
(74) PHILLIPS ORMONDE FITZPATRICK, 367 Collins Street, Melbourne,<br />
Victoria 3000, Australia<br />
(57) A tool storage device is disclosed. The tool storage device comprises<br />
a hollow upright pivot shaft having two ends, a top end and a bottom end<br />
where the pivot shaft is end capped on the top and bottom ends, and a<br />
tool storage means coupled to the hollow upright pivot shaft. Each end<br />
cap has a coupling wall and a plughole formed in the coupling wall. A<br />
plurality <strong>of</strong> detachable connecting structures are provided, each having<br />
a plug rod attachable to each end cap through the plughole. A plurality <strong>of</strong><br />
fastening structures comprise a base having a plurality <strong>of</strong> apertures for<br />
fastening to an upright support structure. Each fastening structure comprising<br />
a coupling unit detachably connectable to the connecting structure<br />
at the top and bottom ends <strong>of</strong> the capped hollow upright pivot shaft.<br />
(21) 568025 (22) 25 Apr 2006<br />
(54) Process for the preparation <strong>of</strong> fipronil, an insecticide, and related<br />
pyrazoles<br />
(86) PCT/IB2006/000999 (87) WO2007/122440<br />
(51) IPC2011.01:C07D231/44<br />
(71) Gharda Chemicals Limited<br />
(72) Gharda, Keki Hormusji; Malte, Ashokkumar Maganlai; Joseph,<br />
Pulinattu Cherian; Parkar, Sureshkumar Dattatraya; Sathe, Shekhar<br />
Vishwanath; Damania, Pragnesh Dalpatram;<br />
(74) PHILLIPS ORMONDE FITZPATRICK, 367 Collins Street, Melbourne,<br />
Victoria 3000, Australia<br />
(57) Disclosed is a process for the preparation <strong>of</strong> 5-amino-1-phenyl-3cyano-4-trifluoromethyl<br />
sulphinyl pyrazoles as defined by Formula-I,<br />
wherein: R1 = trifluoromethyl or trifluoromethoxy, and R2 and R3 are<br />
individually hydrogen, chlorine or bromine, the process comprising the<br />
step <strong>of</strong> oxidizing a compound <strong>of</strong> Formula-II wherein: R1 = trifluoromethyl<br />
or trifluoromethoxy, R2 and R3 = individually hydrogen, chlorine or bromine,<br />
in a medium comprising at least one oxidizing agent and trichloro<br />
acetic acid, and/or the reactions product (s) <strong>of</strong> the at least one oxidizing<br />
agent and trichloro acetic acid, and at least one melting point depressant<br />
selected from monochloro acetic acid, dichloro acetic acid, methylene<br />
dichloride, ethylene dichloride, monochlorobenzene and a haloalkane.<br />
Also disclosed are 5-amino-1-phenyl-3-cyano-4-trifluoromethyl sulphinyl<br />
pyrazoles as defined by Formula-I obtained by said process.<br />
(21) 568165 (22) 8 Nov 2006<br />
(54) Carton with reinforced handle using a side end reinforcement flap<br />
(86) PCT/US2006/043340 (87) WO2007/056365<br />
(51) IPC2011.01:B65D5/46; B65D71/00<br />
(71) Graphic Packaging International, Inc.<br />
(72) Brand, Kirsten Laura;<br />
(31) 05 734504 (32) 8 Nov 2005 (33) US<br />
(74) PHILLIPS ORMONDE FITZPATRICK, 367 Collins Street, Melbourne,<br />
Victoria 3000, Australia<br />
(57) Disclosed is a carton with a reinforced handle for containing a plurality<br />
<strong>of</strong> articles. The carton comprises: a plurality <strong>of</strong> panels (30, 40) that<br />
extend at least partially around an interior <strong>of</strong> the carton; at least two end<br />
flaps (12, 22, 32) respectively foldably attached to respective panels <strong>of</strong><br />
the plurality <strong>of</strong> panels; and a handle (11) in the closed end <strong>of</strong> the carton<br />
having a handle opening (139) for grasping and carrying the carton. The<br />
plurality <strong>of</strong> panels comprises a top panel (30), a bottom panel, a first side<br />
panel, and a second side panel (40). The end flaps are overlapped with<br />
respect to one another and thereby at least partially form a closed end <strong>of</strong><br />
the carton. The at least two end flaps comprising at least one side end<br />
flap (22, 42) foldably attached to one <strong>of</strong> the first side panel and the second<br />
side panel, and a top end flap (32, 56) foldably attached to the top<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 102 |BACK TO CONTENT
INTELLECTUAL PROPERTY OFFICE OF NEW ZEALAND<br />
panel. The at least one side end flap comprises a main panel (70, 72) for<br />
at least partially closing the closed end <strong>of</strong> the carton and a reinforcement<br />
panel (80, 82) foldably attached to the main panel and upwardly folded<br />
relative to the main panel to at least partially overlap the main panel, the<br />
reinforcement panel cooperating with the main panel to form the handle.<br />
(21) 568407 (22) 17 Nov 2006<br />
(54) Tightening means for anti-skid and traction enhancement devices<br />
(86) PCT/EP2006/068631 (87) WO2007/057450<br />
(51) IPC2011.01:B60C27/10<br />
(71) Emrah Bozkurt; Ender Bozkurt; Murat Yerlikaya<br />
(72) Bozkurt, Emrah; Bozkurt, Ender; Yerlikaya, Murat;<br />
(31) 05110988.2 (32) 18 Nov 2005 (33) EP<br />
(74) PIPERS, Level 1, 5A Pacific Rise, Mt Wellington, Auckland, New<br />
Zealand<br />
(57) A tightening system for use with anti-skid and traction enhancement<br />
devices for wheeled vehicles is disclosed. The system comprises sealed<br />
tightening mechanism which can clutch and ratchet the rotational movement<br />
applied by the user on a knob. The tightening system further comprises<br />
at least one connection assembly which is adapted to be pivotably<br />
and releasably attached to a proximal end <strong>of</strong> a surface contact member<br />
and which is adapted to be connected to the tightening mechanism. The<br />
tightening mechanism comprises a locking component which has a base<br />
plate, an inner sidewall and an outer sidewall standing perpendicular to<br />
said base plate. The inner sidewall recessed portion has a plurality <strong>of</strong><br />
recesses which are adapted to engage with a peripheral projection <strong>of</strong> the<br />
upper clutch for holding the knob in place during locked and unlocked<br />
positions <strong>of</strong> the knob. The outer sidewall enters fully or partly, respectively<br />
in locked and unlocked positions <strong>of</strong> the knob, into a corresponding<br />
slot <strong>of</strong> said knob for sealing inner volume <strong>of</strong> the tightening mechanism<br />
from outside conditions.<br />
(21) 568430 (22) 21 Nov 2006<br />
(54) 4-oxadiazolyl-piperidine compounds and use there<strong>of</strong><br />
(86) PCT/EP2006/011150 (87) WO2007/057229<br />
(51) IPC2011.01:C07D413/04; A61K31/454; A61P25/00; C07D413/14<br />
(71) Purdue Pharma L.P.<br />
(72) Tafesse, Laykea;<br />
(31) 05 739107 (32) 21 Nov 2005 (33) US<br />
(74) F B RICE & CO, Level 23, 44 Market Street, Sydney, New South<br />
Wales 2000, Australia<br />
(57) Disclosed are 4-oxadiazolyl-piperidine compounds as depicted or a<br />
pharmaceutically acceptable salt there<strong>of</strong>, wherein the substituents are<br />
as defined in the specification. Also disclosed are compositions comprising<br />
the 4-oxadiazolyl-piperidine compounds and their use in treating pain<br />
or diarrhea.<br />
(21) 568435 (22) 5 Dec 2006<br />
(54) Method and apparatus for processing <strong>of</strong> materials with bearings supporting<br />
rotating drum being sealed from heat and pressure added in interstitial<br />
space<br />
(86) PCT/US2006/061604 (87) WO2007/117313<br />
(51) IPC2011.01:A61L11/00; B03B3/00<br />
(71) Gordon Craig Boots; Robert D Bartlett; Ryan J Bright; Mark C Woodin<br />
(72) Boots, Gordon C; Bartlett, Robert D; Bright, Ryan J; Woodin, Mark C;<br />
(31) 05 742824 (32) 5 Dec 2005 (33) US<br />
(74) Freehills <strong>Patent</strong> & Trade Mark Attorneys, Level 43, 101 Collins Street,<br />
Melbourne, Victoria 3000, Australia<br />
(57) A treatment vessel has a drum 200 to which pressure and heat can be<br />
applied and rotationally supported within a shell via roller 400. The drum<br />
is supported by bearings 440, 490 which are sealed from pressure and<br />
heat added to the interstitial space between the drum and the shell.<br />
(21) 568512 (22) 16 Aug 2006<br />
(54) Non-peroxide preparation for whitening natural and manufactured teeth<br />
(86) PCT/US2006/031953 (87) WO2007/061468<br />
(51) IPC2011.01:A61Q11/00; A61K8/64,66<br />
(71) TOM’S OF MAINE<br />
(72) Bergeron, Chantal;<br />
(31) 05 281009 (32) 17 Nov 2005 (33) US<br />
(74) A J PARK, 6th Floor, Huddart Parker Building, 1 Post <strong>Office</strong> Square,<br />
Wellington 6011, New Zealand<br />
(57) Disclosed is a peroxide-free method for whitening natural or manufactured<br />
teeth, the method comprising:<br />
(a) providing an actinidin-containing preparation;<br />
(b) formulating the actinidin-containing preparation <strong>of</strong> step (a) for application<br />
to natural or manufactured teeth; and<br />
(c) contacting the formulation <strong>of</strong> step (b) with natural or manufactured<br />
teeth in an amount and for a period <strong>of</strong> time sufficient to effect whitening<br />
<strong>of</strong> the natural or manufactured teeth;<br />
wherein the actinidin-containing preparation is formulated in: a whitening<br />
strip, a dentifrice, a mouthrinse, a mouthwash, chewing gum, a preparation<br />
for soaking manufactured teeth or a whitening tray.<br />
PATENT OFFICE JOURNAL 1580 25 February 2011 Page 103 |BACK TO CONTENT