Retatrutide: research, legal status and who sells it

Retatrutide is an investigational triple hormone receptor agonist from Eli Lilly. It is not approved anywhere we track, and the FDA says it cannot be used in compounding.

By Editorial team. Updated Oct 14, 2026. Awaiting expert review

This page is information, not medical advice. Retatrutide is not approved as a medicine in the markets below unless stated. We don't publish dosing or usage instructions.

Also known as
LY3437943
Category
Investigational GIP, GLP-1 and glucagon receptor triple agonist
Evidence level
Late-stage human trials
Price range
$1.17/mg to $14.50/mg, median $4.69/mg across 22 vendors (compare)
Our lab tests
None yet (how testing will work)
WhereStatus
United StatesNot FDA-approved; FDA states that retatrutide cannot be used in compounding under federal law and has not been found safe and effective for any condition [1].
United KingdomNo UK-licensed medicine containing retatrutide appears in the MHRA products database [2].
European UnionNo medicine containing retatrutide is authorized in the EU, according to EMA's central and Article 57 product data [3][4].
CanadaNo product containing retatrutide appears in Health Canada's Drug Product Database [5].
AustraliaRetatrutide is not named in Australia's Poisons Standard (October 2026) [6].
Sport (WADA)Not named on the 2026 Prohibited List; its section S0 bans any pharmacological substance with no current approval for human therapeutic use [7].
Summaries of official sources, checked Oct 14, 2026. Rules change; follow the source links. Not legal advice.

What it is

Retatrutide (development code LY3437943) is an experimental drug that activates three hormone receptors: GIP, GLP-1 and glucagon [8]. Eli Lilly is testing it in the phase 3 TRIUMPH program for obesity, obstructive sleep apnoea and knee osteoarthritis [9].

Research status

In a 48-week phase 2 trial in 338 adults with obesity, average weight loss reached 24.2% in the highest-dose group, compared with 2.1% on placebo; side effects were mainly gastrointestinal, and heart rate rose in a dose-dependent way [8]. The four TRIUMPH trials together enroll more than 5,800 participants [9]. In TRIUMPH-2, published in 2026, adults with obesity and type 2 diabetes lost 11.9% to 18.8% of body weight over 80 weeks, compared with 5.1% on placebo [10]. Diarrhea, nausea, abnormal skin sensations (dysaesthesia) and low blood pressure were more common with retatrutide, and stopping treatment because of adverse events was more frequent at the two higher doses [10].

Regulatory status

Retatrutide is not approved in the US, the UK, the EU or Canada [11][2][3][5]. The FDA states that retatrutide cannot be used in compounding under federal law, is not a component of any FDA-approved drug and has not been found safe and effective for any condition [1]. The agency says it has warned telehealth companies for marketing retatrutide, ingredient distributors for selling it to compounders, and outsourcing facilities for repackaging it [1]. Retatrutide is not named in Australia’s Poisons Standard [6].

Quality and testing considerations

Because no approved retatrutide product exists, every vial sold online is an unapproved product with no regulator-checked reference to compare against. FDA warning letters have rejected “research use only” labeling when a seller’s own marketing shows that the product is meant for people [12]. The FDA also maintains an import alert for GLP-1 active ingredients with potential quality concerns [1]. Independent identity testing by mass spectrometry, plus measured purity and content, is the minimum needed to know what a vial contains.

Where it’s sold

No approved retatrutide product exists; the tables below track the unapproved “research” listings we monitor.

Retatrutide prices: cheapest listings

The five lowest $/mg listings out of 134. See all Retatrutide prices

Vendor Transparency Product Size Price $/mg vs median Stock Vendor's page
Nova Peptide 45/100* Reta 30 mg × 10 $350 $1.17/mg −75% In stock View
Srylab 25/100 Retatrutide 20 mg × 10 $240 $1.20/mg −74% — View
Nova Peptide 45/100* Reta 20 mg × 10 $250 $1.25/mg −73% In stock View
Nova Peptide 45/100* Reta 15 mg × 10 $195 $1.30/mg −72% In stock View
Srylab 25/100 Retatrutide 15 mg × 10 $195 $1.30/mg −72% — View

Prices come from each vendor's public product feed and were last fetched Oct 15, 2026. They exclude shipping and discounts. $/mg uses the labeled amount, not measured content. A transparency score marked * is based on fewer than six checks; checks we couldn't complete score 0. How we compare prices.

Sources

  1. FDA's Concerns with Unapproved GLP-1 Drugs Used for Weight Loss (content current as of 1 October 2026). U.S. Food and Drug Administration. Accessed Oct 14, 2026
  2. MHRA Products: licensed-medicine search for "retatrutide". Medicines and Healthcare products Regulatory Agency (UK). Accessed Oct 14, 2026
  3. EMA medicines data: centrally authorised human medicines (export of 14 October 2026). European Medicines Agency. Accessed Oct 14, 2026
  4. EMA Article 57 product data: medicines authorised in the EU/EEA (data as of 9 October 2026). European Medicines Agency. Accessed Oct 14, 2026
  5. Drug Product Database online query (searched by active ingredient). Health Canada. Accessed Oct 14, 2026
  6. Therapeutic Goods (Poisons Standard—October 2026) Instrument 2026 (F2026L01327, registered 30 September 2026). Federal Register of Legislation, Australian Government. Accessed Oct 14, 2026
  7. World Anti-Doping Code International Standard: Prohibited List 2026 (in force 1 January 2026). World Anti-Doping Agency. Accessed Oct 14, 2026
  8. Triple-Hormone-Receptor Agonist Retatrutide for Obesity: A Phase 2 Trial. New England Journal of Medicine (2023). Accessed Oct 14, 2026
  9. Retatrutide for obesity, obstructive sleep apnea and knee osteoarthritis: rationale and design of the TRIUMPH trials. Diabetes, Obesity and Metabolism (2026). Accessed Oct 14, 2026
  10. Retatrutide in adults with obesity and type 2 diabetes (TRIUMPH-2): a phase 3 trial. The Lancet (2026). Accessed Oct 14, 2026
  11. Drugs@FDA: FDA-Approved Drugs (database searched by active ingredient). U.S. Food and Drug Administration. Accessed Oct 14, 2026
  12. Warning Letter to USApeptide.com (MARCS-CMS 696885), 26 February 2025. U.S. Food and Drug Administration. Accessed Oct 14, 2026