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PharmAthene Reports Year-End 2009 Financial and Operational Results and Provides Update On Ongoing Litigation With SIGA Technologies
Date:3/23/2010

Also in February 2010 PharmAthene submitted a White Paper seeking further development funding for SparVax™, in response to a Broad Agency Announcement (Solicitation Number: BAA-BARDA-09-34).

"PharmAthene ended the year with a solid biodefense portfolio having made progress in all areas of our business," said David P. Wright, President and Chief Executive Officer. "The additional development funding for our SparVax™ anthrax vaccine program announced in February could allow us to offer a promising improved alternative to existing anthrax vaccine options.  Phase I clinical trial results for Protexia® provided important confirmation of its safety and lack of immunogenicity in humans.  These results, along with accumulating data in animal models, which have shown that Protexia® is capable of preventing toxicity from exposure to chemical nerve agents, suggest an important role for Protexia® in preventing or possibly treating the toxic effects of nerve agents.  Finally, recent non-clinical data from our Valortim® program demonstrate a novel ability to potentially augment the immune system's response to anthrax bacteria, an exciting finding, which we continue to explore in greater depth.  We enter 2010 with significant momentum and the potential to achieve significant additional contract funding for our biodefense programs."


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SOURCE PharmAthene, Inc.
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1. PharmAthene to Provide Update on SparVax(TM) Contract Modification Suspension During Year-End 2009 Financial and Operational Results Conference Call on Tuesday March 23, 2010
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4. PharmAthene Submits White Paper to BARDA for Advanced Development Funding for SparVax(TM) - Novel Recombinant Protective Antigen Anthrax Vaccine
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