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Metabolic Research99% purity · HPLCAvailable to orderResearch use only

RT Tri-Agonist

Triple GIP/GLP-1/glucagon receptor agonist (investigational peptide)

Also known as GIP/GLP-1/glucagon triple agonist RT; development code LY3437943

An investigational single-molecule agonist of the GIP, GLP-1 and glucagon receptors, currently in late-stage clinical development. Not an approved medicine anywhere as of this profile.

RT Tri-Agonist research peptide vial, Positive Peptides, 99% purity
RT Tri-Agonist research peptide vial, Positive Peptides, 99% purity

Technical information

Values are shown with their status. “Verified” means the value has been checked against a primary database such as PubChem.

Classification
Triple GIP/GLP-1/glucagon receptor agonist (investigational peptide)
CAS number
2381089-83-2 Pending
Molecular formula
C221H342N46O68 Pending
Molecular weight
4731.3 g/mol Pending
Sequence / structure
39-aa acylated peptide (see data source) Pending

Some values are still being checked and should be treated as provisional until marked verified.

How this compound is tested

As for other acylated multi-agonist peptides: LC-MS intact mass and HPLC purity. Reference standards for an investigational compound may be scarce; the COA should state what reference material, if any, was used.

Research background

RT Tri-Agonist extends the multi-agonist concept by adding glucagon receptor activity to GIP/GLP-1 agonism. Glucagon receptor agonism is of interest for its effects on hepatic lipid metabolism and energy expenditure in preclinical models. The compound is under development by Eli Lilly and is investigational; it has not completed regulatory review.

Mechanisms investigated in published research

These are the mechanisms examined in the cited literature. Describing them is not a claim that the compound produces any effect in humans.

  • Triple agonism at GIP, GLP-1 and glucagon receptors, with activity balanced across the three in engineered assays.
  • Investigation of hepatic fat, energy expenditure and glucose regulation in animal models and early human studies.
Summary of evidence

Laboratory and animal findings are kept separate from human clinical evidence.

Preclinical findings

Rodent studies during development reported body-weight and metabolic effects attributed to combined receptor activation.

Human clinical evidence

1 cited

A phase 2 randomised trial in adults with obesity (Jastreboff et al., 2023; n = 338) reported dose-dependent changes in body weight over 48 weeks. Phase 3 trials are ongoing. Phase 2 data are preliminary and the product remains investigational; no regulatory approval exists.

Limitations and open questions
  • Investigational status: safety and efficacy have not been established by regulators.
  • Phase 2 sample sizes are small and durations short relative to phase 3.
  • Research-grade material is not the clinical investigational product.

Scientific references

Publications cited on this page. Links open the publisher or PubMed record.

  1. [1]Jastreboff AM, Kaplan LM, Frías JP, et al.. Triple-hormone-receptor agonist retatrutide for obesity — a phase 2 trial. New England Journal of Medicine (2023).

    Human clinical Citation pending

    Phase 2; investigational product.

Research use only

RT Tri-Agonist is described here for laboratory research. It is not approved for human or veterinary use unless a regulator has said otherwise, and nothing on this page is medical advice or guidance on administration. A disclaimer does not by itself make any activity lawful. Full disclaimer.

Contact options

Talk to the Positive Peptides team about RT Tri-Agonist

Order enquiries, documentation requests and technical questions about this compound — we answer directly, usually within two working days.

For laboratory research only. All compounds described on this website are supplied strictly for in-vitro laboratory research. They are not for human or veterinary use, and no medical or therapeutic claims are made. Researchers remain responsible for complying with the rules that apply to them.

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