Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**Setrobuvir + danoprevir + ritonavir** is an investigational oral combination regimen studied for the treatment of chronic hepatitis C virus (HCV) infection, particularly genotype 1. Setrobuvir is a direct-acting antiviral (DAA) that acts as a non-nucleoside inhibitor of the HCV RNA-dependent RNA polymerase (NS5B). Danoprevir is a macrocyclic inhibitor of the HCV NS3/4A serine protease, while ritonavir acts as a pharmacokinetic enhancer (booster) that increases danoprevir plasma concentrations by inhibiting CYP3A metabolism. The combination has been studied in interferon-free regimens, often together with ribavirin and/or mericitabine. Clinical studies have demonstrated efficacy (as measured by sustained virologic response rates) and an acceptable safety profile in treatment-naive patients with HCV genotype 1[1][2][4].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on setrobuvir + danoprevir + ritonavir.