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FDA committees meet to investigate Testosterone Deficiency therapy

Read time: 1 mins
Last updated: 22nd Jul 2014
Published: 22nd Jul 2014
Source: Pharmawand

On 17 September the FDA's Bone, Reproductive and Urologic Drugs panel will convene with the Drug Safety and Risk Management committee to assess the appropriate indicated population for Testosterone Replacement Therapy and the potential for adverse cardiovascular outcomes associated with testosterone drugs. Recently judges in Chicago consolidated a number of cases brought against against Abbott and AbbVie which sell AndroGel; Eli Lilly which makes Axiron; Pfizer ( for its injectable version; and Actavis for its testosterone patch.

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