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A Parallel-Group Treatment, Phase 2, Double-Blind Study of Once-Weekly Subcutaneous LY3457263 Compared to Placebo in Participants With Type 2 Diabetes Mellitus on a Stable Dose of Semaglutide or Tirzepatide Who Failed to Achieve HbA1c Goal
The purpose of this study is to measure the change in hemoglobin A1c (HbA1c) with LY3457263 compared with placebo in participants with type 2 diabetes who are not at HbA1c goal when treated with a stable dose of semaglutide or tirzepatide. Participation in the study will last about 9 months.
Details
| Lead sponsor | Eli Lilly and Company |
|---|---|
| Phase | Phase 2 |
| Status | RECRUITING |
| Enrolment | 240 |
| Start date | 2025-03-28 |
| Completion | 2027-01 |
Conditions
- Type 2 Diabetes
Interventions
- LY3457263
- Placebo
Primary outcomes
- Change from Baseline in Hemoglobin A1c (HbA1c) — Baseline, Week 24
Countries
United States, Canada, Germany, Poland, Puerto Rico, United Kingdom