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🇪🇺EU · EMAAuthorisedATC: R07AX33Orphan Medicine

Alyftrek(deutivacaftor;tezacaftor;vanzacaftor calcium dihydrate)

Cystic Fibrosis

Marketing Authorisation Holder: Vertex Pharmaceuticals (Ireland) Limited

EMA Authorisation: 30/06/2025

INN: deutivacaftor / tezacaftor / vanzacaftor

Indication

Alyftrek tablets are indicated for the treatment of cystic fibrosis (CF) in people aged 6 years and older who have at least one non-Class I mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene (see sections 4.2 and 5.1).

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.