RAPIVAB(TM) Trial Results for the Treatment of Influenza to be Presented at IDWeek 2014
Three posters will be presented on
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Poster 827 titled "The Efficacy of Single Dose Peramivir in Acute Uncomplicated Influenza; an Integrated Subject Level Meta-Analysis," by
Richard Whitley , M.D. et al. -
Poster 1169 titled "Safety of Peramivir in Hospitalized Influenza," by
Sylvia M. Dobo , M.D. et al. -
Poster 1171 titled "The Development of Influenza Virus Variants with Reduced Susceptibility Following Peramivir Treatment: An Analysis of Clinical and Post-Marketing Experience," by
Phil Collis , Ph.D. et al.
The posters are available at the Company's peramivir publications page.
The New Drug Application (NDA) for the indication of treatment of acute uncomplicated influenza in adults is currently under regulatory review by the
About RAPIVAB
RAPIVAB is a potent, intravenously administered, investigational anti-viral agent that rapidly delivers high plasma concentrations to the sites of influenza infection. If approved, RAPIVAB would be the first and only one-dose intravenous treatment for acute, uncomplicated influenza in the U.S. In laboratory tests, RAPIVAB has shown activity against multiple influenza strains, including H7N9 and pandemic H1N1 swine flu viral strains. RAPIVAB was developed under a
About BioCryst
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CONTACT:Source:Robert Bennett ,BioCryst Pharmaceuticals , +1-919-859-7910 (investors)Mariann Caprino , FleishmanHillard, +1-917-242-1087 (media)
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