Rapid Licensure of a New, Inactivated Influenza Vaccine in the United States

 Abstract

Background: The unexpected problems at 1 of 2 US licensed manufacturers of trivalent inactivated influenza virus vaccine (TIV) in 2004 highlights the urgent need for additional vaccine sources. We evaluated a split virus TIV (Fluarix, GSK), to generate data supportive of a license application in the US.
Methods: Healthy adults ages 18-64 years at 4 centers were randomly assigned to receive a single IM injection of Fluarix (n=763) or placebo (n=193) in double-blind fashion. Subjects were monitored for safety and serum hemagglutination-inhibition (HAI) titers determined before and 21 days after vaccination.
Results: Vaccine was well tolerated, with only mild to moderate myalgias and injection site pain and redness being more common in vaccine than placebo recipients. Four-fold or greater increases in serum HAI titers were seen in 60%, 62%, and 78% of vaccine recipients against the H1, H3, and B components of the vaccine, respectively, and post-vaccination titers of > 1:40 achieved in 98%, 99%, and 99% of subjects, exceeding the pre-specified criteria for acceptability for all three antigens.
Conclusions: Fluarix has a safety and immunogenicity profile like other US-licensed inactivated influenza vaccines and should be effective when used to immunize US adults.

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Pages
239 - 244
doi
10.4161/hv.1.6.2376
Type
Research Paper
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Rapid Licensure of a New, Inactivated Influenza Vaccine in the United States