Woman and Man
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Extract
The primary objectives of this study are: • To determine the efficacy of GS-7977 + RBV as measured by the proportion of subjects with sustained viral response at 12 weeks after discontinuation of therapy (SVR12). • To evaluate the safety and tolerability of GS-7977 + RBV as assessed by review of the accumulated safety data.
Inclusion criteria
- Chronic Genotype 2 or 3 HCV Infection