Woman and Man
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Extract
The primary objectives of this study are: * To compare the efficacy of treatment with sofosbuvir (SOF)/GS-5816 fixed dose combination (FDC) for 12 weeks with that of SOF + ribavirin (RBV) for 24 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 each treatment regimen
Inclusion criteria
- Chronic hepatitis C virus infection