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What phase is retatrutide in?

Retatrutide is in phase 3: the TRIUMPH programme consists of four phase 3 randomized trials of weekly subcutaneous retatrutide against placebo in over 5800 participants.

GLP-1 / GIP / glucagon triple agonistUpdated

Short answer

Retatrutide is in phase 3: the TRIUMPH programme consists of four phase 3 randomized trials of weekly subcutaneous retatrutide against placebo in over 5800 participants.[1]

Which phase 3 trials have reported

TRIUMPH-1, a phase 3 trial in adults with obesity without diabetes, assigned participants to 4, 9 or 12 mg or placebo weekly for 80 weeks.[2]

A phase 3 trial in type 2 diabetes describes retatrutide as under clinical development for diabetes, obesity and related complications.[3]

Not every study is phase 3: TRANSCEND-CKD is a phase 2b mechanistic trial in chronic kidney disease.[4]

Drugs@FDA still returns no match for retatrutide, so phase 3 has not yet produced an approved product in that database.[5]

More on Retatrutide

Sources

  1. 1Retatrutide for the treatment of obesity, obstructive sleep apnea and knee osteoarthritis: Rationale and design of the TRIUMPH registrational clinical trials.Diabetes, obesity & metabolism · 2026PMID 41090431Accessed 2 Oct 2026
  2. 2Retatrutide, a Triple Hormone Receptor Agonist, for Treatment of Obesity.The New England journal of medicine · 2026PMID 42814954Accessed 2 Oct 2026
  3. 3Efficacy and safety of retatrutide, a GIP, GLP-1, and glucagon receptor agonist, in people with type 2 diabetes and inadequate glycaemic control with diet and exercise (TRANSCEND-T2D-1): a double-blind, randomised, phase 3 trial.Lancet (London, England) · 2026PMID 42250575Accessed 2 Oct 2026
  4. 4Rationale, design and baseline characteristics of the TRANSCEND-CKD trial of retatrutide in patients with chronic kidney disease.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2026PMID 41160422Accessed 2 Oct 2026
  5. 5Drugs@FDA (openFDA) search: active ingredient "retatrutide"U.S. Food and Drug Administration · 2026api.fda.govAccessed 2 Oct 2026

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