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Nov 19, 2012
 |  BC Week In Review  |  Clinical News  |  Regulatory

Q-Pan H5N1 adjuvanted regulatory update

FDA's Vaccines and Related Biological Products Advisory Committee voted 14-0 that safety and immunogenicity data support accelerated approval of Q-Pan H5N1 adjuvanted vaccine from GlaxoSmithKline to prevent disease in adults who are at an increased risk of exposure to the influenza A virus subtype H5N1. The panel was divided on the non-voting topic of the options by which GSK can confirm Q-Pan H5N1's clinical benefit...

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