Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Harvoni is a fixed-dose combination drug containing ledipasvir and sofosbuvir, developed by Gilead Sciences for the treatment of chronic hepatitis C virus (HCV) infection. Ledipasvir is an inhibitor of the HCV NS5A protein, which is essential for viral replication and assembly. Sofosbuvir is a nucleotide analog that inhibits the HCV NS5B RNA-dependent RNA polymerase, acting as a chain terminator during viral RNA synthesis. This combination is highly effective across multiple HCV genotypes (1, 4, 5, and 6). In the context of Tanta University, it has been evaluated in Phase 4 clinical trials for efficacy in pediatric patients with beta-thalassemia and HCV infection, specifically monitoring liver fibrosis markers like hyaluronic acid.
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 ledipasvir + sofosbuvir.