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Study in humans · 2023 · cited for Retatrutide

Triple-Hormone-Receptor Agonist Retatrutide for Obesity - A Phase 2 Trial

Jastreboff AM, Kaplan LM, Frías JP, Wu Q, Du Y, Gurbuz S, et al. The New England journal of medicine 2023;389(6):514-526. doi:10.1056/NEJMoa2301972 · PubMed 37366315

In brief

Retatrutide is a single peptide acting on the GIP, GLP-1 and glucagon receptors. This trial enrolled 338 adults, just over half men, with a body-mass index of 30 or more, or 27 or more with a weight-related condition, and gave weekly retatrutide at maintenance doses of 1, 4, 8 or 12 milligrams, or placebo, for 48 weeks. At 24 weeks, the primary endpoint, weight had fallen 7.2 percent on 1 milligram, 12.9 percent on 4, 17.3 percent on 8 and 17.5 percent on 12, against 1.6 percent on placebo, and losses continued to 48 weeks; every participant on 12 milligrams lost at least 5 percent and 83 percent lost at least 15 percent. Gastrointestinal events were the most common adverse effects, dose-related and mostly mild to moderate, and were reduced by a lower starting dose. Heart rate rose with dose, peaking at 24 weeks. Funded by Eli Lilly.

Study design

Phase-2, double-blind, randomised, placebo-controlled trial, 338 adults with obesity, retatrutide at four maintenance doses or placebo weekly for 48 weeks.

What it does not show

A phase-2 trial of 48 weeks with no long-term safety data, sponsor-funded, in a pharmaceutical form under medical supervision. It is not an approved drug and the compound is still in phase-3 trials.

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 — Phase 2, 338 adults with obesity: mean weight change of −24.2% at 48 weeks on 12 mg weekly, against −2.1% on placebo.

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.