TRIUMPH-8NCT07232719
A Study of Retatrutide (LY3437943) in Participants With Obesity or Overweight
StatusActive, Not Recruiting
PhasePhase 3
SponsorEli Lilly and Company
Primary completion (estimated)
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Record History
All 5 versions: 5 with changes below. See every version on ClinicalTrials.gov ↗
- Notable Eligibility criteria expanded, about 16 words
- Study completion pushed from Jul 2027 to Jun 2028
- Primary completion date: Jul 2027 to Jun 2027
- Site details revised at 2 of 31 sites
- Minor Trial status changed: Recruiting → Active, Not Recruiting
- Site details revised at 31 of 31 sites
- Minor Site details revised at 25 of 31 sitesv3
- Notable Trial status: Not Yet Recruiting to Recruiting
- Study sites: 32 to 31
- Start date changed from estimate of Dec 2025 to Nov 17, 2025
- Study First Submitted
- Notable: the plan changed
- Minor: routine updates
Endpoints
Primary
Percent Change from Baseline in Body Weight
Timeframe: Baseline, Week 56
Secondary (4)
Change from Baseline in Systolic Blood Pressure
Change from Baseline in Waist Circumference
Percent Change from Baseline in Non-High-Density Lipoprotein (HDL) Cholesterol
Pharmacokinetics (PK): Steady State Area Under the Concentration Time Curve (AUC)
Arms and interventions
Retatrutide Dose 1Experimental
Participants will receive retatrutide subcutaneously (SC)
Retatrutide Dose 2Experimental
Participants will receive retatrutide SC
PlaceboPlacebo comparator
Participants will receive placebo SC
Drugs: Retatrutide, Placebo
Sites
31 sites in 2 countries
United States 19, United Kingdom 12