Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This is a **triple combination therapy** used to treat chronic hepatitis C virus (HCV) infection, especially genotypes 1 and 4. - **Sofosbuvir** is a nucleotide analog **NS5B polymerase inhibitor** that blocks HCV RNA replication. - **Pegylated interferon alfa-2a** is a **recombinant cytokine** that induces antiviral immune responses via the **interferon alpha receptor**, modulating immune activity and limiting viral replication. - **Ribavirin** is a **nucleoside analog** that broadly inhibits viral RNA synthesis and impairs viral genetic fidelity. This combination is used for 12 weeks in genotype 1 or 4 HCV and sometimes in genotype 1 patients who are interferon-eligible. Phase 3 clinical data confirm superior efficacy compared to historical controls, with sustained virologic response (SVR) rates around 90% for 12 weeks of therapy. The combination is **approved for use** in the United States for HCV genotypes 1 and 4, and is recommended in patients with or without cirrhosis, but **is not recommended for patients with severe renal impairment or decompensated liver disease**. Most common adverse effects are fatigue, headache, nausea, insomnia, and anemia[1][3][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 sofosbuvir + pegylated interferon alfa-2a + ribavirin.