Effect of Retatrutide Compared With Placebo in Adult Participants With Type 2 Diabetes and Inadequate Glycemic Control With Diet and Exercise Alone (TRANSCEND-T2D-1)
Part of paid clinical trials in Scottsdale, Arizona.
- Sponsor
- Eli Lilly and Company
- Study ID
- NCT06354660
- Phase
- PHASE3
- Status
- Completed
Conditions
- Diabetes Type 2
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 investigate the efficacy and safety of retatrutide compared with placebo in participants with Type 2 Diabetes and inadequate glycemic control. The study will last about 11 months and may include up to 11 visits.
Key Dates
- Start date
- Apr 10, 2024
- Status verified
- Mar 2026
- Primary completion
- Jan 22, 2026
- Completion
- Feb 20, 2026
Study Design
- Enrollment
- 537 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Retatrutide Dose Level 1Participants will receive retatrutide administered subcutaneously (SC).
- Experimental: Retatrutide Dose Level 2Participants will receive retatrutide administered SC.
- Experimental: Retatrutide Dose Level 3Participants will receive retatrutide administered SC.
- Placebo Comparator: PlaceboParticipants will receive placebo administered SC.
Primary Outcome Measure
Change from Baseline in Hemoglobin A1c (HbA1c) (%) [ Time Frame: Baseline, Week 40 ]
Locations (29)
Related coverage on Hipa.ai
- Retatrutide Phase 3 Trial for Type 2 Diabetes Completes Primary Data CollectionRetatrutide · Jan 22, 2026 · ClinicalTrials.gov
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