Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Furaprevir (TG-2349) and yimitasvir (DAG-181) are direct-acting antiviral agents developed as an all-oral combination therapy for the treatment of chronic hepatitis C virus (HCV) infection. Furaprevir is a small molecule NS3/NS4A protease inhibitor that blocks viral replication by inhibiting the HCV serine protease required for polyprotein processing. Yimitasvir is a small molecule NS5A inhibitor that interferes with viral RNA replication and assembly. The combination has been evaluated in multiple clinical trials, including Phase III studies in HCV genotype 1 infected patients, both with and without cirrhosis. The regimen may also be used with ribavirin in some protocols[1][2][3][4][5][6][7][8]. Developed through a joint venture between TaiGen Biotechnology and YiChang HEC ChangJiang Pharmaceutical (HEC), this fixed-dose cocktail targets improved sustained virologic response rates for hepatitis C.
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 furaprevir + yimitasvir.