Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
ASC43F is a first-in-class, dual-targeting fixed-dose combination (FDC) tablet developed by Gannex Pharma (a subsidiary of Ascletis Pharma) for the treatment of metabolic dysfunction-associated steatohepatitis (MASH), formerly known as non-alcoholic steatohepatitis (NASH). The drug consists of a once-daily single tablet containing 5 mg of ASC41, a thyroid hormone receptor beta (THRβ) agonist, and 15 mg of ASC42, a farnesoid X receptor (FXR) agonist. These two components possess complementary mechanisms of action: THRβ agonists primarily exert anti-metabolic effects to reduce hepatic fat, while FXR agonists provide anti-fibrotic and anti-inflammatory benefits. By combining these modalities, ASC43F is designed to work synergistically to target all major components of MASH, including steatosis, ballooning, inflammation, and fibrosis. Phase I clinical results in healthy subjects have demonstrated that the combination is safe and well-tolerated.
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 ASC43F.