Overview

Efficacy and Safety of Orforglipron in Participants With Peripheral Artery Disease

Status:
NOT_YET_RECRUITING
Trial end date:
2028-06-01
Target enrollment:
Participant gender:
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.
Phase:
PHASE3
Details
Lead Sponsor:
Eli Lilly and Company
Treatments:
orforglipron