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Study in humans · 2022 · cited for Retatrutide

LY3437943, a novel triple glucagon, GIP, and GLP-1 receptor agonist for glycemic control and weight loss: From discovery to clinical proof of concept

Coskun T, Urva S, Roell WC, Qu H, Loghin C, Moyers JS, et al. Cell metabolism 2022;34(9):1234-1247.e9. doi:10.1016/j.cmet.2022.07.013 · PubMed 35985340

In brief

LY3437943, later named retatrutide, is one peptide that activates three receptors: glucagon, GIP and GLP-1. In cell assays it showed balanced activity at the glucagon and GLP-1 receptors and more at the GIP receptor. In obese mice it reduced body weight and improved glycaemic control, and the authors attribute the extra weight loss over dual agonists to glucagon-receptor-driven energy expenditure added to the intake reduction from GIP and GLP-1 signalling. In a phase-1 single-ascending-dose study, safety and tolerability were similar to other incretin drugs, the pharmacokinetics supported once-weekly dosing, and a reduction in body weight persisted to day 43 after one dose. The authors conclude further clinical assessment is warranted.

Study design

Discovery-to-clinic paper for LY3437943: receptor pharmacology, obese-mouse studies and a phase-1 single-ascending-dose study.

What it does not show

A single-dose first-in-human study alongside mouse work, written by the developer. The phase-2 trials cited with it are where the weight and glucose results in people come from.

A clinical trial tests a pharmaceutical form of a compound, in a defined patient group, under medical supervision, with a defined endpoint. None of that transfers to a research-grade vial, and this page does not suggest it does.

Where this paper is cited

  • Retatrutide — The discovery paper: how the three receptor activities were balanced in one molecule, with first-in-human data supporting once-weekly dosing.

Other papers cited for Retatrutide

Further reading

How this page was made: the citation was retrieved from PubMed by PMID and checked against the title on the product page; the summary was written from the paper's abstract and reports only what the abstract reports. Read the paper itself before relying on any figure here.

Research use only This page summarises a published paper. It is not a claim that any product sold by Zyrna Research does what the paper describes, the trial used a pharmaceutical product under medical supervision, and nothing here is dosing guidance. Nothing sold by Zyrna Research is for human or veterinary use.