Monday, November 2, 2009

GTx Receives Complete Response Letter from FDA for Toremifene 80 mg New Drug Application

Nov 2, 2009 - GTx, Inc. today announced that it has received a Complete Response Letter issued by the United States Food and Drug Administration (FDA) regarding its New Drug Application (NDA) for toremifene 80 mg to reduce fractures in men with prostate cancer receiving androgen deprivation therapy (ADT).

The details can be read here.

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