Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
NCO-48 fumarate is an orally administered small molecule prodrug of tenofovir being developed by Nucorion Pharmaceuticals for the treatment of chronic hepatitis B virus (HBV) infection. As a nucleotide analog, it is metabolized into its active form, tenofovir, which acts by inhibiting the HBV reverse transcriptase enzyme, thereby blocking viral DNA synthesis and replication. In clinical evaluations, NCO-48 fumarate has been studied in Phase 1 trials to assess its safety, pharmacokinetics, and antiviral activity in treatment-naive adults, comparing its efficacy and safety profile to tenofovir alafenamide (TAF).
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 NCO-48 fumarate.