Retatrutide
An experimental once-weekly shot that acts on three hormone receptors: GIP, GLP-1 and glucagon. In phase 3 trials for obesity and type 2 diabetes.
- Evidence
- Ongoing clinical research
- Half-life
- ~6 days
- Sources
- 3 cited
Is retatrutide FDA-approved?
Investigational. Not FDA-approved.
Overview
Retatrutide is Eli Lilly's investigational "triple agonist." In a 48-week phase 2 trial, adults with obesity on the highest dose lost about 24% of their body weight on average, versus about 2% on placebo. Phase 3 trials are testing it for obesity, type 2 diabetes, knee osteoarthritis pain, sleep apnea, and heart and kidney outcomes. Versions sold online as "research peptides" are not the studied drug.
How it works
The GLP-1 and GIP parts curb appetite and help insulin release. The glucagon part raises the body's energy use and pushes the liver to burn more fat.
How long does retatrutide stay in the body?
About 6 days in early human studies, which supports weekly shots.
What it's studied for
- Obesity
- Type 2 diabetes
- Fatty liver disease
- Knee osteoarthritis pain
- Heart and kidney outcomes
Reported side effects
- Nausea, diarrhea, vomiting, constipation (mostly when the dose goes up)
- Higher resting heart rate, dose-related
Related: Tirzepatide, Semaglutide, Lixisenatide, Cagrilintide. Compare: Retatrutide vs tirzepatide.
Sources
The studies and prescribing labels this page is written from.
- Triple-Hormone-Receptor Agonist Retatrutide for Obesity: A Phase 2 Trial. N Engl J Med, 2023 PubMed
- Retatrutide for people with type 2 diabetes: a phase 2 trial. Lancet, 2023 PubMed
- LY3437943 in people with type 2 diabetes: a phase 1b trial. Lancet, 2022 PubMed