Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
GI-5005 + peginterferon alfa + ribavirin is a combination therapy formerly investigated for the treatment of chronic hepatitis C virus (HCV) genotype 1 infection. The regimen consists of GI-5005, a Tarmogen therapeutic vaccine comprising heat-inactivated recombinant Saccharomyces cerevisiae yeast expressing a fusion of HCV NS3 and Core proteins, administered alongside the standard of care (SOC) components peginterferon alfa and ribavirin. GI-5005 was designed to stimulate an HCV-specific T-cell immune response to reduce the viral load in infected cells. Despite showing immunogenicity and some improvements in ALT levels in Phase 2 trials, the triple combination failed to significantly improve sustained virologic response (SVR) rates compared to SOC alone in treatment-naive patients or those who had previously failed therapy. Consequently, GlobeImmune discontinued the development of GI-5005 for HCV.
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 GI-5005 + peginterferon alfa + ribavirin.