A study testing whether a GLP-1 medicine from Lilly, orforglipron, can improve blood flow in the legs.
- Who can join
- Adults 18+, have peripheral artery disease (poor blood flow in the legs), BMI 23+.
- What you take
- orforglipron, given as part of the study at no cost to you. Some participants may receive a placebo (an inactive version) instead, decided at random.
- How long it lasts
- The full study runs about 2.7 years; your own time in it is usually shorter.
- What you get
- The study medication and study-related care at no cost. Compensation varies by study site; many cover travel and provide the study medication at no cost. The trial coordinator will explain what that site offers before you join.
What this study is for
Full study title: Efficacy and Safety of Orforglipron in Participants With Peripheral Artery Disease.
Primary condition: Peripheral Arterial Disease.
Who can join, in detail
Key inclusion criteria
- Have symptomatic PAD with intermittent claudication of Fontaine Stage II
- Have an Ankle Brachial Index (ABI) of 0.9 or less
Key exclusion criteria
- Have a body mass index (BMI) less than 23 kilogram per square meter (kg/m2)
- Have Hemoglobin A1c (HbA1c) greater than 10%
- Have walking ability limited by conditions other than PAD
- Have a planned lower limb surgery or any other surgery affecting walking ability
- Had peripheral revascularization procedure within 90 days prior to the day of screening or planning to undergo peripheral revascularization during the clinical trial
Where this study is enrolling
This trial has 30 US sites across 13 states. Contact the site coordinator directly to start the screening process.
Alabama
- St. Vincent's Birmingham HospitalBirmingham, Alabama
Arizona
- Mercy Gilbert Medical CenterGilbert, Arizona602-214-0886
- Axsendo Clinical Research - Peak Heart & Vascular - SurpriseSurprise, Arizona844-290-2273
- Del Sol Research Management, LLCTucson, Arizona520-257-3881
California
- Valley Clinical Trials, Inc.Northridge, California818-280-4220
- The Cardiovascular CenterRedding, California281-944-3610
- InvivoCureVan Nuys, California859-509-0084
- Interventional Cardiology Medical GroupWest Hills, California818-702-8800
Florida
- Lakeview Institute of Clinical ResearchLeesburg, Florida352-782-0606
- Inpatient Research ClinicMiami Lakes, Florida786-502-4303
- Floridian Clinical Research, LLCMiami Lakes, Florida305-330-9977
- St Johns Center for Clinical ResearchSaint Augustine, Florida904-209-0043
Indiana
- ASHA Clinical Research - Munster, LLCHammond, Indiana219-803-6649
- Indiana University Health Methodist HospitalIndianapolis, Indiana
- Deaconess Clinic- GatewayNewburgh, Indiana812-490-4505
Maryland
- Flourish Research - BowieBowie, Maryland410-824-1341
Michigan
- Arcturus Healthcare , PLC, Troy Internal Medicine Research DivisionTroy, Michigan248-312-0025
Pennsylvania
- Capital Area Research, LLCCamp Hill, Pennsylvania717-441-1725
Tennessee
- The Jackson ClinicJackson, Tennessee731-660-8396
- East Coast Institute for Research - Jefferson CityJefferson City, Tennessee
Texas
- Biopharma Informatic, LLCHouston, Texas281-944-3610
- Research Physicians Network, LLCHouston, Texas832-847-1724
- Sherman Clinical ResearchSherman, Texas903-771-4093
- NextStage Clinical Research - WacoWaco, Texas
Utah
- Alpine Research OrganizationClinton, Utah801-791-2206
Virginia
- Stroobants Cardiovascular CenterLynchburg, Virginia
- Clinical Research Partners, LLCRichmond, Virginia804-477-3045
- Gershon Pain SpecialistsVirginia Beach, Virginia757-496-2050
Washington
- ERA Health Research - CardioNow - LynnwoodLynnwood, Washington425-869-6828
- Eastside Research AssociatesRedmond, Washington425-869-6828
Timeline
Started enrolling: 2025-10-31. Expected completion: 2028-06. Last updated on ClinicalTrials.gov: 2026-05-22.
Official source
We sync this data quarterly from ClinicalTrials.gov, the federal registry for clinical research. Before contacting a site, verify the trial is still recruiting on the official page:
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