Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**EMP16** is an oral, modified-release fixed-dose combination of **orlistat** and **acarbose** being developed by Empros Pharma for chronic weight management and obesity. The formulation is designed to release the locally acting agents in targeted regions of the gastrointestinal tract to improve the efficacy-tolerability balance of conventional formulations. Orlistat inhibits gastrointestinal lipases and reduces dietary triglyceride hydrolysis and fat absorption, while acarbose inhibits intestinal carbohydrate-digesting enzymes, delaying carbohydrate digestion and glucose absorption. Phase 2 studies have reported placebo-adjusted weight loss and no unexpected safety findings, while an additional Phase 2 pilot study evaluated gastrointestinal tolerability during dose escalation with dietary fiber support.
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 EMP16 (Empros Pharma).