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Retatrutide Guide

What Is Retatrutide?

Retatrutide (LY3437943) is a first-in-class triple incretin receptor agonist developed by Eli Lilly — a single engineered peptide that simultaneously activates the GIP, GLP-1 and glucagon receptors. In Phase 2 research it produced the largest weight reduction reported for any compound in the incretin class to date. This guide explains what it is, how it works, and where the research currently stands.

Research reference · Reviewed 2026 · For in vitro laboratory use only
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Laboratory research compound — in vitro use only
Retatrutide is supplied by RS Bio Labs strictly as a laboratory research material for qualified scientific personnel. It is not approved, intended or authorised for human consumption, self-administration, diagnostic, therapeutic or veterinary use. All findings referenced here are from published preclinical or clinical-trial literature and do not constitute medical advice or establish safety in any unapproved setting.

Retatrutide in one sentence

Retatrutide is a synthetic, fatty-acid-conjugated long-acting peptide that binds and activates three related metabolic receptors at once — the glucose-dependent insulinotropic polypeptide receptor (GIPR), the glucagon-like peptide-1 receptor (GLP-1R) and the glucagon receptor (GCGR). Because it engages all three pathways, it is described in the literature as a "triple agonist" or "GGG tri-agonist", and it sits one generation beyond dual agonists such as Tirzepatide (GIP/GLP-1).

Developer codeLY3437943
ClassTriple GIP / GLP-1 / Glucagon agonist
OriginatorEli Lilly & Co.
Molecular weight~4,731 Da
ModificationC20 fatty-acid conjugate
Half-life~6 days
Research scheduleOnce weekly
Regulatory statusInvestigational — not approved

How does Retatrutide work?

The defining feature of Retatrutide is that a single molecule acts on three receptors that each sit at a different node of the body's energy-balance network. The combined effect is qualitatively different from any single- or dual-agonist compound:

In short, Retatrutide is studied as a compound that reduces energy intake (via GLP-1/GIP) while simultaneously increasing energy expenditure (via glucagon) — a combination not achievable with monotherapy. For a deeper breakdown of how these three receptor systems differ, see GLP-1 vs GIP vs Glucagon agonists.

Why is Retatrutide significant?

The Phase 2 TRIUMPH-1 trial (Jastreboff et al., New England Journal of Medicine, 2023) studied Retatrutide in adults with obesity over 48 weeks. At the 12 mg dose, mean body-weight reduction reached approximately 24.2% — the largest effect reported for any incretin-class compound to date, and notably the dose-response curve had not plateaued by week 48. A parallel Phase 2 programme in metabolic dysfunction-associated steatohepatitis (MASH) reported substantial reductions in liver-fat content. Phase 3 development (including cardiovascular outcomes) is ongoing.

How it compares

Semaglutide (GLP-1) delivered ~15% and Tirzepatide (GIP/GLP-1) ~22.5% in their respective pivotal trials. Retatrutide's ~24% at 48 weeks — still climbing — is what places the triple-agonist mechanism at the frontier of incretin research.

CompoundReceptor targetsPeak trial weight change
RetatrutideGIP + GLP-1 + Glucagon~24.2% (Ph2, 48 wk)
TirzepatideGIP + GLP-1~22.5% (Ph3, 72 wk)
SemaglutideGLP-1~15% (Ph3, 68 wk)

Forms, handling & half-life

Research-grade Retatrutide is supplied as a sterile lyophilised (freeze-dried) powder in sealed vials, measured in milligrams. Before use in a research setting it is reconstituted with bacteriostatic water; the vial is then kept refrigerated. Three companion guides cover the practical handling in detail:

Research status & safety context

As of 2026, Retatrutide remains an investigational compound. It has not been approved by the MHRA, FDA or any other regulator for any use, and it is not available as a medicine. Everything documented above is drawn from published clinical-trial and preclinical literature and is provided as a scientific reference only. Products sold by RS Bio Labs are research reagents for in vitro laboratory work and are not for human use.

Retatrutide — Research Grade
≥99% purity, third-party HPLC tested, with a Certificate of Analysis. Free UK shipping · dispatched 1–2 business days. Available in eight strengths — a selection shown below.
Retatrutide 10mg
LY3437943 · lyophilised
Retatrutide 30mg
LY3437943 · lyophilised
Retatrutide 60mg
LY3437943 · best value
Bacteriostatic Water
10ml · for reconstitution
View all Retatrutide strengths & GLP-1 compounds →
Quick Retatrutide FAQs
Is Retatrutide the same as Tirzepatide?+
No. Tirzepatide is a dual GIP/GLP-1 agonist, while Retatrutide adds a third target — the glucagon receptor — making it a triple agonist. See our full Retatrutide vs Tirzepatide comparison.
What is Retatrutide's half-life?+
Approximately six days, owing to its C20 fatty-acid conjugation and albumin binding — which is why research protocols use a once-weekly schedule. More detail in the half-life guide.
How is Retatrutide supplied?+
As a sterile lyophilised powder in sealed vials (5–60 mg), each with a third-party Certificate of Analysis confirming ≥99% purity. It is reconstituted with bacteriostatic water before use — see reconstituting Retatrutide.
Is Retatrutide approved or legal to use?+
Retatrutide is an investigational compound not approved by any regulator. RS Bio Labs supplies it solely as a research reagent for in vitro laboratory use — not for human consumption.
Continue the Retatrutide series