Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
ANA975 is an orally bioavailable prodrug of isatoribine (ANA245), a small molecule toll-like receptor 7 (TLR7) agonist. Developed by Anadys Pharmaceuticals in collaboration with Novartis, it was primarily investigated for the treatment of chronic hepatitis C virus (HCV) infection. ANA975 is designed to be converted into the active nucleoside analog isatoribine through hydrolysis by esterases and oxidation by aldehyde oxidase. By activating TLR7, a pattern-recognition receptor, the drug triggers the innate immune response, specifically inducing interferon-alpha and other cytokines to inhibit viral replication. Clinical development was discontinued in July 2007 following Phase I trials because toxicology studies indicated that chronic daily dosing was unlikely to provide an adequate therapeutic index for the treatment of 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 ANA975.