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🇪🇺EU · EMAAuthorisedATC: J05AR

Genvoya(elvitegravir;cobicistat;emtricitabine;tenofovir alafenamide)

HIV Infections

Marketing Authorisation Holder: Gilead Sciences Ireland UC

EMA Authorisation: 19/11/2015

INN: elvitegravir;cobicistat;emtricitabine;tenofovir alafenamide

Indication

Genvoya is indicated for the treatment of adults and adolescents (aged 12 years and older with body weight at least 35 kg) infected with human immunodeficiency virus 1 (HIV 1) without any known mutations associated with resistance to the integrase inhibitor class, emtricitabine or tenofovir.

Official EMA Resources

View on EMA (ema.europa.eu)

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Medical disclaimer: This information is intended for qualified healthcare professionals. Always verify with the official EMA Summary of Product Characteristics (SmPC) before clinical use.