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🇪🇺EU · EMAAuthorisedATC: J05AR

Delstrigo(doravirine;lamivudine;tenofovir disoproxil fumarate)

HIV Infections

Marketing Authorisation Holder: Merck Sharp & Dohme B.V.

EMA Authorisation: 22/11/2018

INN: doravirine;lamivudine;tenofovir disoproxil

Indication

Delstrigo is indicated for the treatment of adults infected with HIV 1 without past or present evidence of resistance to the NNRTI class, lamivudine, or tenofovir. Delstrigo is also indicated for the treatment of adolescents aged 12 years and older weighing at least 35 kg who are infected with HIV-1 without past or present evidence of resistance to the NNRTI class, lamivudine, or tenofovir and who have experienced toxicities which preclude the use of other regimens that do not contain tenofovir disoproxil.

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.