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Merck & Co. Submits FDA Application for Cervical Cancer Vaccine
December 6, 2005 On Dec. 1, Merck & Co. submitted an application for U.S. Food and Drug Administration approval of its cervical cancer vaccine Gardasil, which is engineered to protect against four types of human papillomavirus. Merck is seeking to get a priority review designation for Gardasil and said it expects FDA's decision in about two months. The drug company also plans this month to submit applications to license the vaccine in Europe and Asia. Back to other news for December 6, 2005 Wall Street Journal 12.06.05; Dow Jones Newswires This article was provided by U.S. Centers for Disease Control and Prevention. It is a part of the publication CDC HIV/Hepatitis/STD/TB Prevention News Update. |