A Study of Orforglipron (LY3502970) Compared With Dapagliflozin in Adult Participants With Type 2 Diabetes and Inadequate Glycemic Control With Metformin
Part of paid clinical trials in Canoga Park, California.
- Sponsor
- Eli Lilly and Company
- Study ID
- NCT06192108
- Phase
- PHASE3
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Orforglipron — DRUGAdministered orally
- Dapagliflozin — DRUGAdministered orally
Study Details
The main purpose of this study is to assess the safety and efficacy of orforglipron compared with dapagliflozin in improving blood sugar control in participants with type 2 diabetes (T2D) with inadequate glycemic control using metformin. The study will last approximately 46 weeks.
Key Dates
- Start date
- Jan 10, 2024
- Status verified
- Oct 2025
- Primary completion
- Sep 26, 2025
- Completion
- Sep 26, 2025
Study Design
- Enrollment
- 962 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Orforglipron Dose 1Participants will receive orforglipron orally.
- Experimental: Orforglipron Dose 2Participants will receive orforglipron orally.
- Experimental: Orforglipron Dose 3Participants will receive orforglipron orally.
- Active Comparator: DapagliflozinParticipants will receive dapagliflozin orally.
Primary Outcome Measure
Change from Baseline in Hemoglobin A1c: (HbA1c) [ Time Frame: Baseline, Week 40 ]
Locations (19)
Related coverage on Hipa.ai
- Dapagliflozin Phase 3 Trial vs Orforglipron in Type 2 Diabetes CompletesDapagliflozin · Sep 26, 2025 · ClinicalTrials.gov
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