A Study of Retatrutide (LY3437943) in the Maintenance of Weight Reduction in Individuals With Obesity
Part of paid clinical trials in Santa Ana, California.
- Sponsor
- Eli Lilly and Company
- Study ID
- NCT06859268
- Phase
- PHASE3
- Status
- Active Not Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Retatrutide — DRUGAdministered SC
- Placebo — DRUGAdministered SC
Study Details
This is a study of retatrutide in participants with obesity. The main purpose is to learn more about how retatrutide maintains body weight loss. The study will have two treatment phases: an 80 week lead-in phase in which all participants will take retatrutide dose 1 and a 36 week randomized, double-blinded phase in which participants will either take retatrutide dose 1, retatrutide dose 2, or switch to placebo. Participation in the study will last around 125 weeks.
Key Dates
- Start date
- Mar 5, 2025
- Status verified
- Feb 2026
- Primary completion
- Apr 30, 2028
- Completion
- Apr 30, 2028
Study Design
- Enrollment
- 643 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Retatrutide Dose 1Participants will receive retatrutide dose 1 administered subcutaneously (SC) for 116 weeks
- Experimental: Retatrutide Dose 1 to Retatrutide Dose 2Participants will receive retatrutide dose 1 administered SC for 80 weeks, then retatrutide dose 2 administered SC for an additional 36 weeks
- Placebo Comparator: Retatrutide Dose 1 to PlaceboParticipants will receive retatrutide dose 1 administered SC for 80 weeks, then placebo administered SC for an additional 36 weeks
Primary Outcome Measure
Percent Change from Baseline in Body Weight [ Time Frame: Week 0, Week 116 ]
Locations (33)
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