Preserved supervised synthesis

Retatrutide synthesis · version 1

This URL preserves the exact reviewed public wording and source set for synthesis version 1.

Supervised synthesis pilot

What do selected human studies report about Retatrutide?

Manually reviewed August 18, 2026 · version 1

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A bounded review of two sponsor-funded randomized Phase 2 trials: one in obesity and one in type 2 diabetes.12

Bottom line from this bounded source set

Both reviewed Phase 2 trials reported reductions in body weight, and the type 2 diabetes trial also reported lower glycated hemoglobin. These mid-stage studies do not resolve long-term outcomes or broader population effects.12

Reviewed study record

Phase 2 obesity trial

Design

A double-blind, randomized, placebo-controlled Phase 2 trial followed participants for 48 weeks and assessed body-weight change and safety.1

Population

The trial enrolled 338 adults with obesity, or overweight plus at least one weight-related condition.1

Outcomes reported

At 48 weeks, reported mean body-weight change ranged from -8.7% to -24.2% across retatrutide groups, compared with -2.1% for placebo. Gastrointestinal events were the most common adverse events, and heart-rate increases peaked at 24 weeks before declining.1

Limitations

This was a sponsor-funded Phase 2 trial with 48-week follow-up; it was not a long-term cardiovascular-outcomes or rare-harms study.1

Reviewed study record

Phase 2 type 2 diabetes trial

Design

A randomized, double-blind, placebo- and active-comparator-controlled Phase 2 trial evaluated glycated hemoglobin at 24 weeks and body weight at 36 weeks.2

Population

The trial randomized 281 adults with type 2 diabetes and elevated body-mass index at 42 U.S. centers; 275 were included in efficacy analyses.2

Outcomes reported

At 24 weeks, reported glycated-hemoglobin changes ranged from -0.43 to -2.02 percentage points across retatrutide groups, compared with -0.01 for placebo and -1.41 for the active comparator. Reported body-weight change at 36 weeks ranged from -3.19% to -16.94% across retatrutide groups.2

Limitations

The sponsor-funded trial had 36-week follow-up, 79% completed treatment, and 84% of participants were White; those features limit conclusions about durability and generalizability.2

Reviewed source set

  1. PubMed · 37366315Triple-Hormone-Receptor Agonist Retatrutide for Obesity - A Phase 2 Trial ↗PubMed PMID 37366315 · EFetch XML reviewed 2026-08-18 · payload SHA-256 167232d6f5d1818faabbc3d98c283b2ffad85563d5e10720f8e23347bba1ad1b
    No registered Crossref update in the reviewed snapshotChecked August 19, 2026 for DOI 10.1056/nejmoa2301972. This bounded result is not proof that the publication has never been corrected or retracted. Open the pinned Crossref work endpoint ↗
  2. PubMed · 37385280Retatrutide, a GIP, GLP-1 and glucagon receptor agonist, for people with type 2 diabetes: a randomised, double-blind, placebo and active-controlled, parallel-group, phase 2 trial conducted in the USA ↗PubMed PMID 37385280 · EFetch XML reviewed 2026-08-18 · payload SHA-256 766a11f2d979da96a8a2b79353159b0e0472215d1e391b8f8f5d09a142c5fdcd
    No registered Crossref update in the reviewed snapshotChecked August 19, 2026 for DOI 10.1016/s0140-6736(23)01053-x. This bounded result is not proof that the publication has never been corrected or retracted. Open the pinned Crossref work endpoint ↗