Descovy

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U.S. Food and Drug Administration Approves…

Fixed-Dose Combination HIV Treatment Backbone Can…

Gilead Sciences, Inc. (NASDAQ: GILD) today announced that the U.S. Food and Drug Administration (FDA) has approved Descovy® (emtricitabine 200 mg/tenofovir alafenamide 25 mg, F/TAF), a fixed-dose combination for the treatment of HIV. Descovy is indicated in combination with other antiretroviral agents for the treatment of HIV-1 infection in adults and pediatric patients 12 years of age and older.  Descovy is not indicated for use as pre-exposure prophylaxis (PrEP) to reduce the risk of sexually acquired HIV-1 in adults at high risk. See below for Important Safety Information, within the press release. The full Prescribing Information, including BOXED WARNING, is available for download within the DOCUMENTS tab.  CONTACTS:       Patrick O’Brien, Investors - (650) 522-1936 Ryan McKeel, Media - (650) 377-3548

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