EUROPEAN COMMISSION GRANTS MARKETING AUTHORIZATION FOR GILEAD’S EPCLUSA® ▼(SOFOSBUVIR/VELPATASVIR) FOR THE TREATMENT OF ALL GENOTYPES OF CHRONIC HEPATITIS C

Oprettet 11/07/2016 – 07:32

The European Commission has granted marketing authorization for Epclusa (sofosbuvir 400 mg/velpatasvir 100 mg), the first pan-genotypic, single tablet regimen for the treatment of adults with genotype 1-6 chronic hepatitis C virus (HCV) infection.

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