A Study of Retatrutide (LY3437943) in Participants With Type 2 Diabetes Mellitus Who Have Obesity or Overweight
Part of paid clinical trials in Anniston, Alabama.
- Sponsor
- Eli Lilly and Company
- Study ID
- NCT05929079
- Phase
- PHASE3
- Status
- Active Not Recruiting
Conditions
- Obesity
- Obstructive Sleep Apnea
- Overweight
- Type 2 Diabetes
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Retatrutide — DRUGAdministered SC
- Placebo — DRUGAdministered SC
Study Details
The purpose of this study is to is to evaluate the efficacy and safety of retatrutide in participants with type 2 diabetes in participants who have obesity or overweight (J1I-MC-GZBK master protocol) including a subset of participants who have obstructive sleep apnea (OSA) (J1I-MC-GSA2). The study will last about 89 weeks and will include up to 24 visits.
Key Dates
- Start date
- Jul 11, 2023
- Status verified
- Apr 2026
- Primary completion
- May 31, 2026
- Completion
- May 31, 2026
Study Design
- Enrollment
- 1,000 participants (estimated)
- 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.
- Experimental: Retatrutide Dose 3Participants 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 (40)
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