A Study of Retatrutide (LY3437943) in Participants With Obesity and Cardiovascular Disease
Part of paid clinical trials in Phoenix, Arizona.
- Sponsor
- Eli Lilly and Company
- Study ID
- NCT05882045
- Phase
- PHASE3
- Status
- Completed
Conditions
- Cardiovascular Diseases
- Obesity
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Retatrutide — DRUGAdministered SC
- Placebo — DRUGAdministered SC
Study Details
The main purpose of this study is to evaluate the efficacy and safety of retatrutide once weekly in participants with obesity and established cardiovascular disease (CVD). The study will last about 113 weeks.
Key Dates
- First listed
- May 31, 2023
- Start date
- May 30, 2023
- Status verified
- Jul 2026
- Primary completion
- Apr 16, 2026
- Completion
- May 14, 2026
Study Design
- Enrollment
- 1,946 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Retatrutide Dose 1Participants will receive retatrutide subcutaneously (SC).
- Experimental: Retatrutide Dose 2Participants will receive retatrutide SC.
- Placebo Comparator: PlaceboParticipants will receive placebo.
Primary Outcome Measure
Percent Change from Baseline in Body Weight [ Time Frame: Baseline, Week 80 ]
Locations (46)
Related coverage on Hipa.ai
- Retatrutide Phase 3 Trial for Obesity and CVD Reaches Primary CompletionRetatrutide · Apr 30, 2026 · ClinicalTrials.gov
- Retatrutide Phase 3 Study for Obesity and CVD Reaches Primary CompletionRetatrutide · Apr 16, 2026 · ClinicalTrials.gov
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