Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
BMS-986171 is a subcutaneously administered pegylated variant of fibroblast growth factor 21 (FGF21) developed by Bristol Myers Squibb. It acts as a fibroblast growth factor replacement and is classified as an antifibrotic, fibroblast growth factor, and hepatoprotectant. The drug was primarily investigated for the treatment of non-alcoholic steatohepatitis (NASH) and hepatic fibrosis. Preclinical studies in animal models demonstrated that BMS-986171 improved liver steatosis and fibrosis, supporting its therapeutic potential in NASH. However, no recent clinical development has been reported beyond early-phase trials[1][5][7].
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 BMS-986171.