Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Deutaleglitazar (AB-101) is a deuterated small molecule dual agonist of peroxisome proliferator-activated receptors alpha (PPARα) and gamma (PPARγ). Developed by Alebund Pharmaceuticals, it is a deuterated analog of aleglitazar, a compound originally developed for type 2 diabetes and cardiovascular disease. The incorporation of deuterium is intended to enhance the metabolic profile and safety of the drug by reducing the formation of toxic metabolites or slowing clearance. Deutaleglitazar is currently being evaluated in Phase II clinical trials for the treatment of chronic kidney diseases, specifically diabetic kidney disease (DKD) and IgA nephropathy (IgAN), where it is expected to provide renal protection through its effects on lipid metabolism, insulin sensitivity, and inflammation.
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 deutaleglitazar.