Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This drug is a **combination** of **inarigivir soproxil** and **tenofovir alafenamide**, developed primarily as an oral treatment for **chronic hepatitis B virus (HBV) infection**. Inarigivir soproxil is an immunomodulatory small molecule prodrug and a retinoic acid-inducible gene I (RIG-I) agonist that stimulates the intracellular innate immune response, activating RIG-I and possibly NOD2 (nucleotide-binding oligomerization domain-containing protein 2), leading to the production of interferons and antiviral cytokines[2][3][6][7]. Tenofovir alafenamide is a nucleotide reverse transcriptase inhibitor (NRTI) that directly inhibits HBV DNA polymerase, blocking viral replication. The combination's hypothesis was to achieve both direct antiviral suppression (via tenofovir alafenamide) and immune stimulation (via inarigivir), aiming for functional HBV cure. Development of the combination was **terminated** due to safety concerns, specifically **hepatotoxicity** observed in trials involving inarigivir[3].
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 inarigivir soproxil + tenofovir alafenamide.