This is a prospective, randomized study to evaluate the efficacy and safety of switching treatment from Peg-interferon and Ribavirin to direct-acting antiviral agents in Chinese with CHC genotype 1b infection, who are interferon/ribavirin-intolerant.
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Proportion of participants with sustained virologic response 12 weeks (SVR12) after discontinuation of therapy
Timeframe: Post treatment Week 12
Proportion of participants with adverse events leading to permanent discontinuation of study drug(s)
Timeframe: Baseline up to Week 24