drugset / Trial / NCT07223593
Efficacy and Safety of Orforglipron in Participants With Peripheral Artery Disease
RandomizedParallel-groupDouble-blindTreatment
Summary
The purpose of this study is to evaluate the effect and safety of orforglipron once daily in participants with Fontaine II peripheral arterial disease (PAD). Participation in the study will last about 58 weeks.
Timeline
- Start
- 2025-10-31
- Primary completion
- 2028-06
- Completion
- 2028-06
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Orforglipron | Small molecule | — | Oral |