Description
Retatrutide is an investigational once-weekly injection being studied for obesity and type 2 diabetes. It acts as a triple agonist, activating the receptors for the hormones GIP (glucose-dependent insulinotropic polypeptide), GLP-1 (glucagon-like peptide-1), and glucagon. This medication can be used to help control appetite and manage blood sugar. As of 2026, it has not been approved by the U.S. Food and Drug Administration (FDA), Health Canada, or other regulators, and it is available only through clinical trials.
| Fact Table |
| Formula |
C221H342N46O68 |
| License |
None; investigational, not FDA-approved |
| Bioavailability |
Not established; studied by subcutaneous injection |
| Legal status |
Investigational; clinical-trial use only |
| Chemical Name |
Retatrutide (LY3437943) |
| Elimination half-life |
Approximately 6 days |
| Dosage (Strength) |
No approved dosage; clinical trials studied 4mg, 9mg, and 12mg once weekly subcutaneously |
| Pregnancy |
Not recommended; no approved pregnancy labeling |
| Brands |
None; not marketed |
| Protein binding |
Not established; lipidated peptide designed for albumin binding |
| PubChem CID |
171390338 |
| MedlinePlus |
Not listed |
| ChEBI |
Not assigned |
| ATC code |
Not assigned |
| DrugBank |
DB18993 |
| KEGG |
D12430 |
| Routes of administration |
Subcutaneous injection |
Directions
Currently, retatrutide should only be used in an approved clinical trial or exactly as directed by a healthcare provider. In phase 2 trials, retatrutide was given as a once-weekly injection under the skin in the abdomen, thigh, or upper arm, on the same day each week. Treatment typically starts at 2 mg once weekly and is slowly increased over several weeks to doses of 4 mg, 8 mg, or 12 mg.
If a dose is missed, follow a healthcare provider’s instructions and do not take two doses at once. Retatrutide is meant to be used along with a reduced-calorie diet and increased physical activity.
Ingredients
The active ingredient is retatrutide.
Cautions
Before using this medication, you may want to consult a healthcare provider about the following:
- Any existing health conditions
- Any allergies
- A list of all medications currently being taken
Retatrutide should only be used under medical supervision, as its long-term safety is not yet fully known.
In studies, higher doses of retatrutide increased heart rate, which peaked around 24 weeks. Your healthcare provider may want to watch your heart rate and blood pressure, especially if you have a heart condition.
Stomach-related side effects such as nausea, vomiting, and diarrhea are common, especially when starting or increasing the dose. Severe or persistent vomiting or diarrhea can lead to dehydration, which may affect the kidneys.
When used in people with type 2 diabetes alongside insulin or medicines that increase insulin release, there may be a higher risk of low blood sugar, also called hypoglycemia. The dose of those other medicines may need to be lowered.
Medicines in the GLP-1 receptor agonist class have been linked to inflammation of the pancreas, also called pancreatitis, and gallbladder problems. Seek medical care for severe stomach pain, fever, or yellowing of the skin or eyes.
Because retatrutide slows stomach emptying, it may affect how food and other oral medications are absorbed.
Contraindications
Based on its drug class and the eligibility rules used in clinical trials, it should be avoided if any of the following apply:
- A known serious allergic, or hypersensitivity, reaction to retatrutide or to any of its ingredients.
- A personal or family history of medullary thyroid carcinoma, or MTC, or Multiple Endocrine Neoplasia syndrome type 2, or MEN 2.
- Pregnancy or breastfeeding, as retatrutide has not been studied in these groups.
Side Effects
The most common side effects of retatrutide reported in clinical trials were gastrointestinal. Side effects are usually mild to moderate, and they often occur when first starting the medication or increasing the dose. Side effects may include:
- Nausea
- Diarrhea
- Vomiting
- Constipation
- Decreased appetite
- Increased heart rate
Retatrutide is still being studied, so all serious side effects may not be fully known yet. Get medical help if you have signs of a severe allergic reaction, such as trouble breathing, a severe rash, or swelling of the face, lips, tongue, or throat. Seek urgent care for severe or persistent stomach pain, especially if it spreads to your back, as this could be a sign of pancreatitis. Contact your healthcare provider if you have severe vomiting, diarrhea, or signs of low blood sugar such as shaking, sweating, confusion, or a fast heartbeat. You should also tell your healthcare provider about any new lump or swelling in your neck, hoarseness, or trouble swallowing.
References
-
Jastreboff AM, Kaplan LM, Frías JP, et al.
Triple-Hormone-Receptor Agonist Retatrutide for Obesity — A Phase 2 Trial
.
N Engl J Med. 2023;389(6):514-526.
-
Rosenstock J, Frias J, Jastreboff AM, et al.
Retatrutide, a GIP, GLP-1 and glucagon receptor agonist, for people with type 2 diabetes: a randomised, double-blind, placebo and active-controlled, parallel-group, phase 2 trial
.
Lancet. 2023;402(10401):529-544.
Frequently Asked Questions about Retatrutide
What is retatrutide?
Retatrutide is an investigational once-weekly injectable medication being studied for obesity, overweight-related conditions, and type 2 diabetes. It is a “triple hormone receptor agonist,” meaning it activates GIP, GLP-1, and glucagon receptors.
Is retatrutide FDA-approved?
No. As of June 2026, retatrutide has not been approved by any regulatory agency and is still being evaluated in clinical trials.
Can I buy retatrutide now?
No. Lilly states that retatrutide is not available for public use and should only be accessed through Lilly-sponsored clinical trials. Products sold online claiming to be retatrutide may be unsafe or counterfeit.
How does retatrutide work?
It targets three hormone pathways involved in appetite, blood sugar, and metabolism: GLP-1, GIP, and glucagon. This is why it is sometimes described as a “triple agonist.”
How much weight loss has retatrutide shown in trials?
In Lilly’s Phase 3 TRIUMPH-1 obesity trial, participants taking 12 mg lost an average of 70.3 lb, or 28.3% of body weight, over 80 weeks. Participants taking 4 mg and 9 mg lost an average of 19.0% and 25.9%, respectively.
Is retatrutide being studied for diabetes?
Yes. Lilly has reported Phase 3 results in adults with type 2 diabetes, and a Lancet-published Phase 3 trial found improvements in blood sugar control and body weight when retatrutide was used as monotherapy in early type 2 diabetes.
What side effects have been reported?
The most common side effects in the TRIUMPH-1 trial were gastrointestinal, including nausea, diarrhea, constipation, and vomiting. These effects generally increased at higher doses.
Is retatrutide the same as Ozempic, Wegovy, Mounjaro, or Zepbound?
No. Retatrutide is a separate investigational drug. Its key difference is that it activates three receptors—GIP, GLP-1, and glucagon—whereas currently marketed incretin medicines target fewer pathways.
Who might retatrutide be for if approved?
It is being studied in adults with obesity, overweight with weight-related conditions, type 2 diabetes, knee osteoarthritis pain, obstructive sleep apnea, chronic low back pain, cardiovascular and renal outcomes, and MASLD. Final approved uses will depend on regulatory review.
Should someone take retatrutide from a peptide or research-chemical seller?
No. Because retatrutide is not approved and is only legally available in clinical trials, non-trial products may contain the wrong ingredient, contaminants, or incorrect dosing. A healthcare professional or official clinical-trial site is the safest route for information.
About Dr. Gerardo Sison (Page Author)
Dr. Sison graduated with honors from the University of Florida. He began his career in pharmacy counseling patients in a community setting and later served in hospitals and clinics. He has also worked in medication therapy management services. Read More....
IMPORTANT NOTE:
The above information is intended to increase awareness of health information and does not suggest treatment or diagnosis. This information is not a substitute for individual medical attention and should not be construed to indicate that use of the drug is safe, appropriate, or effective for you. See your health care professional for medical advice and treatment.
Product Code : 14563