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Mountain View, California

In Jan 2011 VIVUS, Inc. announced that it held a meeting with the US FDA for the New Drug Application for QNEXA. The FDA requested that VIVUS assess the feasibility of analyzing existing healthcare databases to determine the historical incidence of oral cleft in offspring of women treated with topiramate for migraine prophylaxis (100 mg). VIVUS anticipates continued dialog with ...
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Updated30 March 2011

Arena finished clinical testing of lorcaserin in 2009, and filed for Food and Drug Administration approval in December.

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Updated28 May 2010
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