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Wednesday, August 7, 2019

FDA advisory committee backs Gilead’s Descovy for PrEP

An FDA advisory committee voted 16-2 recommending approval of Gilead Sciences’ (GILD -0.2%) Descovy (emtricitabine and tenofovir) for pre-exposure prophylaxis (PrEP) to reduce the risk of sexually acquired HIV-1 infection in men and transgender women who have sex with men.
The FDA’s action date is in October.

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