Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Retatrutide is an investigational peptide drug developed by Eli Lilly for the treatment of obesity and related metabolic conditions. It is a once-weekly, subcutaneous injection that acts as a triple agonist at the glucose-dependent insulinotropic polypeptide (GIP) receptor, glucagon-like peptide 1 (GLP-1) receptor, and glucagon receptor. By simultaneously activating these three receptors, retatrutide targets multiple metabolic pathways to promote weight loss, improve glycemic control, and enhance lipid metabolism. In phase 2 clinical trials, retatrutide demonstrated substantial reductions in body weight—up to 24.2% after 48 weeks—and improvements in cardiometabolic markers such as non-HDL cholesterol and triglycerides. The most common side effects are gastrointestinal in nature during dose escalation. Retatrutide is currently being studied for obesity/overweight management, type 2 diabetes mellitus, fatty liver disease (including NASH), and cardiovascular risk reduction[1][4][5][7][9][10].
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 retatrutide.