In development · Not FDA approved

Retatrutide

Eli Lilly’s triple agonist — the first drug to average 30% weight loss in a phase 3 trial.

Drug class: Triple GIP / GLP-1 / glucagon agonist
Status: Investigational — phase 3 complete, not approved
Developer: Eli Lilly
Drug classTriple GIP / GLP-1 / glucagon agonist
StatusInvestigational — phase 3 complete, not approved
DeveloperEli Lilly
How takenWeekly injection (in trials)
Avg weight lossUp to ~30.3% at 104 weeks
AvailabilityNot available by prescription
Not available by prescription. Investigational — not FDA approved. Eli Lilly has said it plans to file in Q1 2027. This page tracks the evidence and the timeline — it is not a treatment you can start today.

What is Retatrutide?

Retatrutide is an investigational once-weekly injection from Eli Lilly that activates three receptors at once: GIP, GLP-1, and glucagon. Tirzepatide hits the first two; retatrutide adds the third.

It has produced the largest weight loss numbers ever recorded in an obesity drug trial. In the phase 3 TRIUMPH-1 results reported in May 2026, participants on the top dose averaged 25.0% weight loss at 80 weeks and 30.3% — about 85 lbs — in the 104-week extension, with no plateau in the curve.

It is not approved and cannot be prescribed. On July 23, 2026 Lilly said it plans to file for approval in the first quarter of 2027, pushing back earlier guidance of a 2026 submission. With a standard review that puts a first decision in late 2027 or 2028.

Anything sold today as "retatrutide" — research vials, peptide sites, grey-market sellers — is unapproved and unregulated. No licensed US provider can legally prescribe or dispense it.

How it works

The GLP-1 and GIP arms work the way they do in tirzepatide: appetite drops, the stomach empties more slowly, and insulin response improves. The third arm is what is new.

Glucagon receptor agonism raises energy expenditure and pushes the liver to mobilise stored fat. Historically that was seen as a liability in diabetes drugs, since glucagon raises blood sugar — the bet in retatrutide is that pairing it with two incretin agonists cancels the glucose downside while keeping the metabolic-rate upside. The trial results so far suggest the bet is working.

Dosing schedule

There is no approved dosing schedule — the FDA has not reviewed the drug. These are the weekly doses studied in the phase 3 TRIUMPH program, shown for context only:

DoseWhen
1 mg / weekTitration starting dose in trials
4 mg / weekLowest maintenance dose studied — 17.6% at 80 weeks
9 mg / weekMid dose — 23.7% at 80 weeks
12 mg / weekTop dose studied — 25.0% at 80 weeks, 30.3% at 104 weeks

Results in clinical trials

Up to 30.3% average body weight loss at 104 weeks

TRIUMPH-1, reported in May 2026, found average weight loss of 17.6% at 4 mg, 23.7% at 9 mg, and 25.0% at 12 mg over 80 weeks, versus 3.9% on placebo. In the pre-specified 104-week extension the 12 mg group reached 30.3% — roughly 85 lbs — with the weight curve still falling. At 80 weeks, 45.3% of participants on 12 mg had lost 30% or more of their body weight, a threshold previously associated with bariatric surgery. TRIUMPH-4, in adults with obesity and knee osteoarthritis, showed 28.7% weight loss at 68 weeks alongside significant pain relief.

Side effects

Common

  • Nausea
  • Diarrhea
  • Vomiting
  • Constipation
  • Decreased appetite
  • Increased heart rate

Serious (rare)

  • Pancreatitis (class risk)
  • Gallbladder disease (class risk)
  • Kidney injury from dehydration
  • Effects still under regulatory review
Important: Retatrutide has not completed FDA review, so it carries no approved label, no boxed warning, and no established safety profile for general use. Trial side effects have tracked the GLP-1 class — mostly gastrointestinal, dose-dependent, and worst during titration — but the full risk picture is not settled. Do not buy retatrutide from research-peptide sellers: those products are unapproved, untested for sterility and purity, and illegal to sell for human use.

How much does Retatrutide cost?

There is no legitimate price, because there is no legal way to buy it. What follows is what is known about the eventual market:

RouteTypical cost
Current US priceNot available — not approved
Expected earliest launch2028, if the Q1 2027 filing holds
Grey-market "research" vialsIllegal for human use — avoid entirely
Available alternative todayZepbound (tirzepatide), ~20–22% average weight loss

No US price exists until the FDA approves a drug. For what clinics charge for approved GLP-1s today, see our clinic pricing study.

Frequently asked questions

Is retatrutide FDA approved?

No. As of August 2026 it remains investigational. Lilly announced on July 23, 2026 that it plans to submit for approval in the first quarter of 2027, which puts a first FDA decision in late 2027 or early 2028 and a launch no earlier than 2028.

Can I get retatrutide from a clinic or telehealth provider?

No. No licensed US provider can prescribe it, and no pharmacy can legally dispense it, because it has no FDA approval. Any clinic offering it is operating outside the law, and any website selling vials is selling an unregulated product with no sterility, purity, or dosing guarantees.

How much better is retatrutide than Zepbound?

On trial averages, meaningfully: roughly 25% at 80 weeks and 30.3% at 104 weeks for retatrutide 12 mg, versus about 20–22.5% for tirzepatide. No head-to-head trial has been run, so cross-trial comparisons come with the usual caveats about different populations and protocols.

What should I do while waiting for retatrutide?

If you want treatment now, the approved options are the ones to discuss with a provider — Zepbound and Wegovy for weight management, or the newer oral options if injections are a barrier. Waiting two-plus years for an unapproved drug is rarely the right plan when approved ones are available.

Related medications

Guides

Primary sources

  1. Triple–hormone-receptor agonist retatrutide for obesity (phase 2)New England Journal of Medicine
  2. Retatrutide achieves up to 30.3% average weight loss in phase 3 TRIUMPH-1AJMC

This page is for educational purposes only and is not medical advice. Retatrutide is an investigational drug that has not been approved by the FDA and cannot be legally prescribed or dispensed in the United States. Products sold online under this name are unregulated. GLPFinders is a directory service and does not prescribe, sell, or dispense medications.

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