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Study identifier: NCT07223593 Synced from ClinicalTrials.gov · August 02, 2026
● Recruiting

Efficacy and Safety of Orforglipron in Participants With Peripheral Artery Disease

Condition: Peripheral Arterial Disease  ·  Sponsor: Eli Lilly and Company

PhasePhase 3
Planned participants1205
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or  ·  317-615-4559  ·  LillyTrials@Lilly.com

Physicians interested in becoming principal investigators please contact  ·  clinical_inquiry_hub@lilly.com

Always discuss trial participation with your own doctor first.

Locations (154)

St. Vincent's Birmingham HospitalBirmingham, Alabama, United StatesRecruiting
Mercy Gilbert Medical CenterGilbert, Arizona, United StatesRecruiting
Emvera Health at Peak Heart & Vascular SurpriseSurprise, Arizona, United StatesRecruiting
Del Sol Research Management, LLCTucson, Arizona, United StatesRecruiting
Angel City Research Inc.Los Angeles, California, United StatesNot Yet Recruiting
Valley Clinical Trials, LLC dba Flourish ResearchNorthridge, California, United StatesRecruiting
The Cardiovascular CenterRedding, California, United StatesRecruiting
InvivoCureVan Nuys, California, United StatesRecruiting
Interventional Cardiology Medical GroupWest Hills, California, United StatesRecruiting
Rocky Mountain Regional VA Medical CenterAurora, Colorado, United StatesNot Yet Recruiting
Lakeview Institute of Clinical ResearchLeesburg, Florida, United StatesRecruiting
Inpatient Research ClinicMiami Lakes, Florida, United StatesRecruiting

+ 142 more locations — full list on the registry record.

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