Compound Cluster · Last checked October 7, 2026

Retatrutide Research Hub: Trials & Dosing

Retatrutide is Lilly's once-weekly triple agonist (GLP-1 + GIP + glucagon), still investigational in 2026. This hub points to the page that answers your question: dose math, pen handling, approval status, or UAE sourcing.

Pages
16 retatrutide pages across dosing, approval, and regional context
Clinical stage
Phase 3 — TRIUMPH-1 pivotal obesity readout May 21, 2026 (28.3% at 80 wks, efficacy estimand; 30.3% at 104 wks; NEJM Sep 29, 2026); TRIUMPH-2/-3 positive July 23, 2026; BLA planned Q1 2027
Compliance
For in-vitro laboratory research only. Not for human or veterinary use.

Quick answer — retatrutide research formats (mg per click, 300-click pens)

Start here for UAE & Google-style questions

This hub indexes trials, dosing, and approval pages. For one-pass answers to common UAE retatrutide questions—price, formats, delivery, legality—use the dedicated answer map on the Dubai guide, not scattered paragraphs across the cluster.

Where are the canonical UAE retatrutide answers?

Direct answer: Open the Retatrutide Dubai guide — direct answers for eight extractable blocks: what retatrutide is, trial side effects, vs semaglutide, Dubai price, where to buy in the UAE, six batch-documented formats (of 18 listed) with batch purity, Abu Dhabi/Sharjah delivery, and UAE legality. Supplier checklist: Dubai supplier checklist. Live formats and checkout: Retatrutide UAE verified route. For in-vitro laboratory research only.

Formats-only catalog: #retatrutide-uae-formats · commercial table: Retatrutide UAE formats · pricing: #pricing · COA: #verification.

Pick the right page for your question

The main Research Hub indexes every compound. This page is narrower — just retatrutide. Four common starting points:

Latest readouts · July 23 & September 29, 2026

TRIUMPH-2, TRIUMPH-3 and the TRIUMPH-1 paper

On July 23, 2026 Lilly reported positive toplines from TRIUMPH-2 (obesity with type 2 diabetes, 80 weeks: 12.7% / 19.1% / 20.8% weight loss at 4 / 9 / 12 mg vs 4.0% on placebo; A1C down up to 1.6 points) and TRIUMPH-3 (severe obesity with established cardiovascular disease, 80 weeks: 21.6% / 22.6% at 9 / 12 mg vs 3.2%; MACE-5 HR 0.82, 95% CI 0.55–1.22, not powered for outcomes). Figures use the efficacy estimand. TRIUMPH-1 was published in the New England Journal of Medicine on September 29, 2026: up to 25% weight loss by the treatment-regimen estimand (28.3% by the efficacy estimand). Lilly cites five positive Phase 3 trials. Sources: Lilly, NEJM.

Pivotal readout · May 21, 2026

TRIUMPH-1 pivotal obesity topline

28.3% mean weight loss at 80 weeks on 12 mg (efficacy estimand; n=2,339), rising to 30.3% at 104 weeks in a BMI ≥35 extension. 45.3% of 12 mg participants reached ≥30% weight loss, 65.3% fell below BMI 30. Dose-by-dose AE-driven discontinuation 4.1% / 6.9% / 11.3% vs 4.9% on placebo; dysesthesia up to 12.5% on 12 mg; UTIs noted. Detailed results were presented at the 86th ADA Scientific Sessions in June 2026. Sources: Lilly, TCTMD, AJMC. Full tracker: TRIUMPH trial tracker.

Status snapshot

Phase 3, still investigational

Reviewed October 7, 2026. Lilly reported pivotal TRIUMPH-1 obesity topline results on May 21, 2026 (28.3% mean weight loss at 80 weeks; 30.3% at 104 weeks in the BMI ≥35 extension), on top of the March 19, 2026 TRANSCEND-T2D-1 release. The pipeline page lists retatrutide Phase 3 across obesity, T2D, knee OA, OSA, low back pain, CV/renal outcomes, and MASLD/MASH; TRIUMPH-2 and TRIUMPH-3 reported positive toplines on July 23, 2026, and TRIUMPH-1 was published in NEJM on September 29, 2026. Lilly plans to submit a Biologics License Application (BLA) to the FDA in Q1 2027. Retatrutide is not approved anywhere.

Commercial outlook

BLA submission planned for Q1 2027

At the May 21 readout, a Lilly executive said the company hoped to launch the drug around 2027 after a submission in 2026. Lilly has since set the plan: it intends to submit a Biologics License Application (BLA) to the FDA in Q1 2027, covering obesity, obstructive sleep apnea and knee osteoarthritis pain (Q2 2026 results, August 5, 2026). Any launch depends on FDA review of that submission. Separately, Lilly’s $4.5 billion additional Indiana manufacturing investment (May 6, 2026) expands capacity supporting its obesity and incretin pipeline — which includes retatrutide — rather than naming any single molecule. Sources: CNBC, Lilly Q2 2026, PR Newswire.

Reference format

30 mg pen, 300 clicks

The Remy reference is the 30 mg pen: 300 clicks at 0.1 mg per click, batch RETP002, Janoshik HPLC at 99.262%. Handling on the pen guide, click math on the clicks chart.

Trust layer

Proof and provenance

COA Library, Brand Facts, Editorial Policy, Research Standards, and Contact Verification — the documents behind every claim on these pages.

Section 01

Start here

Six entry points covering the most common retatrutide questions. For quick answers on ordering, COA proof, and delivery, see the Remy Research FAQ page.

Section 02

Fast facts

The headline answers, in case you don't need the deeper page.

Molecule

Lilly's triple agonist

Retatrutide (LY-3437943) is a once-weekly investigational peptide that activates GIP, GLP-1, and glucagon receptors in one compound. Full mechanism on the Retatrutide Profile.

EntityProfile
Status

Phase 3, not approved

Pivotal TRIUMPH-1 obesity topline reported May 21, 2026 (28.3% at 80 wks; 30.3% at 104 wks in BMI ≥35 extension); investigational status unchanged. TRIUMPH-2 and TRIUMPH-3 reported positive toplines on July 23, 2026. Lilly plans a BLA submission to the FDA in Q1 2027; not approved anywhere.

Reviewed October 7, 2026Approval page
Dosing

Three pages, three jobs

Dosage Guide for the titration ladder. Pen Clicks Guide for mg-to-click math. Pen Guide for storage, priming, and device handling.

RoutingPick by intent
Regional

UAE and Saudi are different questions

The UAE pages cover research-use availability, COAs, and supplier verification. The Saudi page is about status interpretation and the approved-product boundary. Use the page that matches your geography.

MarketPick by region
May 2026 Research Update — Cardiology in Review CKM Monograph

A narrative review in Cardiology in Review (Pillai et al, May 11, 2026) re-synthesised retatrutide’s Phase 2 dataset through the lens of cardiovascular-kidney-metabolic (CKM) disease. Key data points: 24.2% mean weight loss at 12 mg over 48 weeks with 63% achieving ≥20% loss; HbA1c −2.02% in T2D with 27% reaching normoglycaemia; DEXA showed 23.2% fat-mass reduction (comparable to bariatric surgery); 82.4% relative reduction in hepatic fat, with liver-fat normalisation in 86%; SBP −8.79 mmHg; significant attenuation of urine albumin-to-creatinine ratio. The review positions retatrutide as a multi-organ CKM agent rather than a weight-loss-only compound.

Section 03

Compound and protocol pages

Mechanism, dosing, safety, and head-to-head comparisons.

Section 04

Handling and dose tools

Pen mechanics, click math, storage, and the calculator.

Section 05

Approval status and regional sourcing

Filing status, trial milestones, and UAE / Saudi context.

Section 06

Retatrutide research FAQ

Direct answers to the most common retatrutide questions, with deeper pages linked from each.

What is retatrutide?

Retatrutide (LY-3437943) is Eli Lilly’s once-weekly investigational triple agonist that activates the GLP-1, GIP, and glucagon receptors in a single peptide. It is in Phase 3 clinical development across obesity, type 2 diabetes, knee osteoarthritis, OSA, low back pain, CV/renal outcomes, and MASLD/MASH. Full mechanism on the retatrutide profile.

Is retatrutide the same as “GLP-3” or “reta peptide”?

Yes — all refer to retatrutide. “Reta” and “reta peptide” are researcher shorthand for retatrutide (LY-3437943). “GLP-3” (or “GLP3”) is an informal label some UAE suppliers use, and it is a misnomer: there is no GLP-3 receptor. Retatrutide is a triple agonist acting on the GLP-1, GIP, and glucagon receptors, which is why it is sometimes marketed as a third-wave “GLP-3.” Full mechanism on the reta entity page and the GLP-1/GIP/glucagon mechanism guide.

Is retatrutide approved in 2026?

No. As of October 7, 2026, retatrutide is investigational — not approved by the FDA, EMA, or UAE MoHAP. Lilly plans to submit a BLA to the FDA in Q1 2027. Lilly reported positive TRIUMPH-1 pivotal obesity topline on May 21, 2026 (28.3% mean weight loss at 80 weeks on 12 mg, efficacy estimand), and TRIUMPH-2 and TRIUMPH-3 on July 23, 2026. Full status: is retatrutide approved?

How many clicks per mg on the 30 mg retatrutide pen?

The 30 mg pen contains 300 clicks at 0.1 mg per click, so 1 mg = 10 clicks, 2 mg = 20 clicks, 4 mg = 40 clicks, 8 mg = 80 clicks, 12 mg = 120 clicks. The dial caps at 60 clicks (6 mg) per dispensing cycle, so targets above 6 mg require more than one dial turn. Full lookup: retatrutide pen clicks guide.

How is retatrutide dosed in Phase 3 trials?

The TRIUMPH and TRANSCEND programmes start at 2 mg once weekly and titrate every 4 weeks, escalating to 4 mg, 8 mg, or 12 mg maintenance arms depending on the trial. Full ladder on the retatrutide dosage guide; direct answers on the dosage FAQ.

What did TRIUMPH-1 show?

Lilly’s May 21, 2026 topline reported 28.3% mean weight loss at 80 weeks on the 12 mg arm (n=2,339), rising to 30.3% at 104 weeks in a BMI ≥35 extension. 45.3% of 12 mg participants reached ≥30% weight loss and 65.3% fell below BMI 30. AE-driven discontinuation was 4.1% / 6.9% / 11.3% across dose arms vs 4.9% on placebo. These figures use the efficacy estimand; by the treatment-regimen estimand the NEJM paper reports up to 25%. Detailed results were presented at the 86th ADA Scientific Sessions in June 2026 and published in the New England Journal of Medicine on September 29, 2026. Tracker: TRIUMPH trial tracker.

Where can retatrutide be sourced in Dubai?

Retatrutide is not available through UAE pharmacies because it is not approved by MoHAP. Research-use supply is available through verified suppliers. Format options and pricing are on the Dubai research guide page, and the supplier verification checklist covers COA checks and channel verification.

How does retatrutide compare to tirzepatide?

Tirzepatide is a dual GIP/GLP-1 agonist already approved as Mounjaro and Zepbound. Retatrutide adds a third receptor (glucagon) and has shown larger Phase 2/3 weight loss numbers (24.2% mean at 12 mg / 48 weeks Phase 2; 28.3% at 80 weeks TRIUMPH-1) versus tirzepatide’s 22.5% at 72 weeks. Full comparison: retatrutide vs tirzepatide vs CagriSema.

What is retatrutide’s half-life and dosing cadence?

Retatrutide has an extended half-life supporting once-weekly subcutaneous administration in clinical trials. Steady-state accumulation and washout details are on the retatrutide half-life page.

Section 07

Primary sources

The official documents this hub's status reading is built on.

Official sources

How to read this

Status before market

If a page mixes approval language with retatrutide, check the approval and trial pages first. Local availability and supplier claims sit downstream of regulatory status, not in place of it.

Why a hub

One molecule, several questions

Retatrutide questions split across mechanism, dosing, approval timing, and regional sourcing. This page keeps the routes to each in one place.