Jan 9, 2009 - Merck & Co., Inc. announced today that the U.S. FDA has issued a second complete response letter regarding the supplemental biologics license application for the use of GARDASIL [Human Papillomavirus Quadrivalent (Types 6, 11, 16, 18) Vaccine, Recombinant] in women ages 27 though 45.
The details can be read here.
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