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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 />

4

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