A Study of Orforglipron for the Maintenance of Body Weight Reduction in Participants Who Have Obesity or Overweight With Weight-Related Comorbidities (ATTAIN-MAINTAIN)
Part of paid clinical trials in Birmingham, Alabama.
- Sponsor
- Eli Lilly and Company
- Study ID
- NCT06584916
- Phase
- PHASE3
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Orforglipron — DRUGAdministered orally
- Placebo — DRUGAdministered orally
Study Details
The main purpose of this study is to evaluate the efficacy and safety of orforglipron on maintenance of body weight reduction in participants who previously completed treatment with injectable tirzepatide (Zepbound) or injectable semaglutide (Wegovy) in the SURMOUNT-5 trial (NCT05822830).
Key Dates
- Start date
- Sep 13, 2024
- Status verified
- Jun 2026
- Primary completion
- Nov 21, 2025
- Completion
- Nov 21, 2025
Study Design
- Enrollment
- 376 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: OrforglipronParticipants will receive orforglipron orally
- Placebo Comparator: PlaceboParticipants will receive placebo orally
Primary Outcome Measure
Percent Maintenance of Body Weight Reduction Achieved in SURMOUNT-5 [ Time Frame: Week 52 ]
Locations (27)
Related coverage on Hipa.ai
- Orforglipron Phase 3 Trial for Obesity, Overweight Completes Primary EndpointOrforglipron · Nov 21, 2025 · ClinicalTrials.gov
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