2012 Annual Report - Prometic - Life Science, Inc.
2012 Annual Report - Prometic - Life Science, Inc.
2012 Annual Report - Prometic - Life Science, Inc.
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SIGNIFICANT EVENTS<br />
20<br />
12<br />
JANUARY<br />
On January 26, <strong>2012</strong>, ProMetic<br />
received a $2.5 million purchase<br />
order under its ongoing supply<br />
agreement with Octapharma,<br />
a leading, Swiss based,<br />
independent global plasma<br />
fractionation company that<br />
specializes in human proteins.<br />
This order related to the<br />
purchase of PrioClear, a<br />
proprietary prion capture resin<br />
incorporated into Octapharma’s<br />
manufacturing process for<br />
its solvent/detergent treated<br />
plasma product, Octaplas LG ® .<br />
Octaplas LG ® is approved for<br />
marketing in several European<br />
countries and the USA<br />
FEBRUARY<br />
On February 17, <strong>2012</strong>, ProMetic<br />
completed its renegotiation of<br />
its long term debt by restructuring<br />
the repayment of $4 million<br />
worth of secured loans previously<br />
provided by some of its long term<br />
stakeholders and improved its<br />
short term liquidity by securing<br />
an additional $1 million equity<br />
investment in ProMetic from one<br />
of the Stakeholders.<br />
MARCH<br />
On March 6, <strong>2012</strong>, ProMetic<br />
signed an agreement with an<br />
existing client to proceed to<br />
the next stage of an ongoing<br />
commercial development<br />
program. This phase of the<br />
commercial development<br />
program called for activities<br />
that provided ProMetic with an<br />
estimated $2.5 million of service<br />
revenues throughout <strong>2012</strong>. An<br />
upfront payment of $0.8 million<br />
was also triggered on the signing<br />
of the agreement.<br />
APRIL<br />
On April 24, <strong>2012</strong>, ProMetic<br />
secured a $1.4 million agreement<br />
with a European biotechnology<br />
manufacturing company. Under<br />
this agreement, ProMetic will<br />
develop an affinity resin product<br />
and its related manufacturing<br />
process providing its client,<br />
a leader in its field, with a<br />
biosimilar product thereby<br />
enhancing the client’s ability<br />
to increase its share of a wellestablished<br />
and lucrative market.<br />
On April 25, <strong>2012</strong>, ProMetic<br />
received a $1.9 million follow-on<br />
purchase order pursuant to<br />
an existing long-term supply<br />
agreement entered into with a<br />
US based biopharmaceutical<br />
company for the manufacturing<br />
of an established bio pharmaceutical<br />
product. This<br />
$1.9 million purchase order<br />
related to the supply of a<br />
proprietary affinity adsorbent<br />
developed and manufactured<br />
by ProMetic’s UK subsidiary,<br />
ProMetic Biosciences Ltd.<br />
MAY<br />
On May 3, <strong>2012</strong>, ProMetic<br />
announced the publication<br />
of the final results of the<br />
Prion-filtered vs. standard<br />
Red cells in Surgical and<br />
Multi-transfused patients<br />
(“PRISM”) study by the UK<br />
Advisory Board for the Safety<br />
of Blood Tissues and Organs<br />
(“SaBTO”).<br />
The final conclusions of the<br />
study were that following<br />
administration of P-Capt ®<br />
filtered red cells to patients:<br />
None of the antibodies found in<br />
study patients were attributable<br />
to use of the filter;<br />
There was no significant<br />
difference in the number of<br />
definite and probable adverse<br />
events in patients receiving<br />
P-Capt ® filtered red cells and<br />
controls patients who received<br />
standard red cells;<br />
The use of the P-Capt ® filter does<br />
not reduce the overall safety of<br />
transfusion (i.e. the filter is safe<br />
to use);<br />
If implemented, the use of<br />
P-Capt ® filters would require<br />
post-marketing surveillance<br />
to assess continued safety in<br />
large populations of transfused<br />
patients.<br />
On May 7, <strong>2012</strong>, ProMetic<br />
signed definitive agreements<br />
with Hematech BioTherapeutics<br />
<strong>Inc</strong>. (“HBI”) for the codevelopment<br />
and co-exclusive<br />
commercialization, on a<br />
world-wide basis (excluding<br />
China), of a plasma-derived<br />
biopharmaceutical product<br />
targeting a rare medical<br />
condition (“Orphan Drug”) and<br />
for a strategic manufacturing<br />
alliance.<br />
ProMetic may receive $10 million<br />
of milestone payments from HBI<br />
which will fund the Orphan<br />
Drug’s development program<br />
up to regulatory approval.<br />
Following the completion of<br />
clinical trials and regulatory<br />
approval, the Orphan Drug will<br />
be commercialized jointly by<br />
ProMetic and HBI on a global<br />
basis (excluding China), with<br />
both parties sharing profits<br />
equally. The Orphan Drug will<br />
be manufactured by ProMetic<br />
in its Laval facility and in HBI’s<br />
planned facility in Taiwan.<br />
The deal includes a strategic<br />
alliance providing HBI rights to<br />
ProMetic’s proprietary PPPS<br />
to manufacture plasma-derived<br />
biopharmaceuticals in a<br />
Taiwanese facility to be built and<br />
operated by HBI.<br />
ProMetic <strong>Life</strong> <strong>Science</strong>s <strong>Inc</strong>.<br />
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