A trial investigating the safety and efficacy of a drug combination Sofosbuvir/Velpatasvir/GS-9857 for subjects with hepatitis C

Update Il y a 4 ans
Reference: EUCTR2015-003455-21

Woman and Man

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Extract

To determine the efficacy of treatment with sofosbuvir (SOF)/velpatasvir (VEL)/GS-9857 fixed dose combination (FDC) for 12 weeks as measured by the proportion of subjects with sustained viral response 12 weeks after cessation of treatment (SVR12) To evaluate the safety and tolerability of treatment with SOF/VEL/GS-9857


Inclusion criteria

  • Chronic hepatitis C virus infection

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