HomeTrialNCT07223593
🔬NCT07223593Phase 3RECRUITING

Efficacy and Safety of Orforglipron in Participants With Peripheral Artery Disease

Study 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.

Interventions / Drugs
View on ClinicalTrials.gov ↗
Study Details
Enrollment1205 participants
Primary Completion
Lead SponsorEli Lilly and Company
Data Retrieved2026-04-11 02:55:33.866366+00:00
Not financial advice. BiotechSigns data is sourced from ClinicalTrials.gov, SEC EDGAR, and other public databases for research and informational purposes only. It does not constitute investment recommendations. Always do your own due diligence before making investment decisions.