GlaxoSmithKline (GSK) announced that the US Food and Drug Administration (FDA) has approved a supplemental biologics license application (sBLA) for its unadjuvanted influenza A (H1N1) pandemic vaccine. The approval of the sBLA, which was filed as a strain change supplement to GSK's FluLaval seasonal flu vaccine, allows the company to manufacture a flu vaccine for use in adults to prevent influenza caused by the 2009 pandemic H1N1 influenza A strain.

The United States Department of Health and Human Services has placed an order to fill 7.6 million doses of unadjuvanted H1N1 pandemic vaccine from GSK, which will contribute to the approximately 250 million doses secured by the US government. The vaccine will be produced in multi-dose vials from bulk vaccine manufactured at GSK's facility in Quebec, Canada. GSK expects to begin shipping vaccine in December and to provide all 7.6 million doses by the end of the year.

Globally, GSK manufactures both adjuvanted and unadjuvanted vaccines to protect against pandemic H1N1 influenza. GSK will supply a vaccine containing a standard dose (15 ug) of inactive influenza virus antigens without an adjuvant for use in the United States. Clinical trials for both GSK's adjuvanted and unadjuvanted vaccines are ongoing in North America, Europe and Japan.

Further information on GSK's development of vaccines to protect against pandemic H1N1 influenza, including explanation of the vaccine development process is available on: www.gsk.com/media/pandemic-flu.htm

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