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FDA Approves Expanded Use of Emergent BioSolutions' BioThrax

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News

FDA Approves Expanded Use of Emergent BioSolutions' BioThrax

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The vaccination schedule for this new indication consists of three doses of BioThrax administered at 0, 2, and 4 weeks post-exposure combined with antimicrobial therapy. BioThrax is the only FDA-licensed vaccine to prevent anthrax.

“Our BioThrax enhancement program is evidence of our successful partnership with the U.S. government to support the nation’s biosecurity efforts. Over the years, we have enhanced the features of BioThrax to include intra-muscular route of administration, a streamlined vaccination schedule, extended shelf life, and now a post-exposure prophylaxis indication. We are proud of these achievements and look forward to continuing to supply the stockpile with this important medical countermeasure,” saidAdam Havey, Executive Vice President and President, Biodefense Division at Emergent BioSolutions.

This expanded indication is supported by data from non-clinical studies, three clinical trials, and a 2010 pre-Phase 3 Vaccines and Related Biological Products Advisory Committee meeting, which confirmed the regulatory pathway for licensure of anthrax vaccines for PEP. BioThrax is the only vaccine to be licensed for post-exposure prophylaxis against anthrax, and is the first vaccine to be licensed using the FDA Animal Rule.

Licensure of BioThrax for PEP is the culmination of a 10-year collaborative effort between Emergent, the Biomedical Advanced Research and Development Authority (BARDA) and the National Institute of Allergy and Infectious Diseases. Studies supporting licensure were funded in part under contract number HHSO-100-2007-00037C provided by BARDA within the Office of the Assistant Secretary for Preparedness and Response in theU.S. Department of Health and Human Services.

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