Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
CDI-31244 + sofosbuvir + velpatasvir is an investigational, oral, short-duration combination therapy for the treatment of chronic hepatitis C virus infection (HCV), specifically genotype 1. This regimen combines CDI-31244, a potent, selective, oral non-nucleoside inhibitor (NNI) of HCV NS5B RNA-dependent RNA polymerase, with sofosbuvir (a nucleotide NS5B polymerase inhibitor) and velpatasvir (an NS5A inhibitor), components of the approved fixed-dose combination Epclusa. CDI-31244 is designed to deliver high concentrations to the liver, with minimal off-target effects on human polymerases, and aims to provide effective HCV therapy with a shorter treatment duration. The combination has shown promising virologic response rates in phase 2 trials, with no significant pharmacokinetic interactions or unexpected safety signals[2][4][5].
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 CDI-31244 + sofosbuvir + velpatasvir.