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A combination experimental antiviral regimen comprising four investigational direct-acting antivirals—RO5466731, RO5190591, RO5024048—and two approved agents, ritonavir and ribavirin, studied primarily for the treatment of chronic hepatitis C (HCV) genotype 1. Each component targets different stages in the HCV life cycle or host-virus interaction, aiming for synergistic viral suppression and improved response in treatment-naïve and interferon null-responder patients. RO5466731, RO5190591, and RO5024048 are Roche investigational DAAs for HCV, while ritonavir acts as a pharmacokinetic enhancer (‘booster’), and ribavirin is a nucleoside analog with broad-spectrum antiviral activity. The development and trials of this combination were led by Hoffmann-La Roche[1][3][5].
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