Gilead receives EU marketing authorization for two doses of Descovy for HIV-1 infection

25 April 2016

US biotech Gilead Sciences (Nasdaq: GILD) has received European marketing authorization for two doses of Descovy (emtricitabine and tenofovir alafenamide), a fixed-dose combination for the treatment of HIV-1 infection.

It is indicated in the European Union for the treatment of adults and adolescents in combination with other HIV antiretroviral agents.

The authorization, allowing for the marketing of Descovy in all 28 countries of the European Union, is based on a Phase III HIV clinical program evaluating F/TAF in combination with other antiretroviral agents in treatment naïve, virologically suppressed, renally impaired and adolescent patients.

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