A study testing whether a GLP-1 medicine from Lilly, orforglipron, can lower blood pressure.
- Who can join
- Adults 18+, have high blood pressure, BMI 25+.
- 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 2.4 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: A Master Protocol for Orforglipron (LY3502970) in Participants With Hypertension and Obesity or Overweight: (ATTAIN-Hypertension Screening).
Primary condition: Hypertension.
Who can join, in detail
Key inclusion criteria
- Has systolic blood pressure (SBP) >= 140 mmHg and/or diastolic blood pressure (DBP) >= 90 mmHg (if DBP criteria alone is met, SBP must be >=130 mmHg) at screening (Visit 1).
- Has SBP >= 140 mmHg and/or DBP >= 90 mmHg (if DBP criteria alone is met, SBP must be >=130 mmHg) at week 0 (Visit 3).
- Untreated for hypertension, or on stable antihypertensive medications >= 30 days prior to Visit 1.
- Have a body mass index (BMI) >= 25 kg/m².
Key exclusion criteria
- Has SBP >=170 mmHg and/or DBP >=110 mmHg at Visit 1 or at Visit 3.
- Has known secondary causes of hypertension
- Have heart failure with reduced ejection fraction (HFrEF) diagnosis
- Have had any of the following conditions within 90 days prior to screening.
- hospitalization for hypertension or for congestive heart failure
Where this study is enrolling
This trial has 29 US sites across 18 states. Contact the site coordinator directly to start the screening process.
Arizona
- Elite Clinical Studies, LLCPhoenix, Arizona
California
- Valley Clinical Trials, Inc.Covina, California
- Valley Clinical Trials, Inc.Northridge, California
Connecticut
- Chase Medical Research, LLCWaterbury, Connecticut
Florida
- Excel Medical Clinical TrialsBoca Raton, Florida
- Care Access - BrandonBrandon, Florida
- Northeast Research Institute - Downtown OfficeJacksonville, Florida
- Care Access - St. PetersburgSt. Petersburg, Florida
Hawaii
- East-West Medical Research InstituteHonolulu, Hawaii
Maryland
- Sinai Hospital Of BaltimoreBaltimore, Maryland
- Ascension Saint Agnes Heart CareBaltimore, Maryland
Massachusetts
- Lucida Clinical TrialsNew Bedford, Massachusetts
Michigan
- Arcturus Healthcare , PLC, Troy Internal Medicine Research DivisionTroy, Michigan
Missouri
- StudyMetrix ResearchCity of Saint Peters, Missouri
Nevada
- Excel Clinical Research, LLCLas Vegas, Nevada
- Palm Research Center SunsetLas Vegas, Nevada
New York
- Rochester Clinical Research, LLCRochester, New York
Ohio
- Remington-Davis, IncColumbus, Ohio
- PriMED Clinical ResearchDayton, Ohio
Oregon
- Advanced Research Institute - TigardTigard, Oregon
South Carolina
- Care Access - MauldinMauldin, South Carolina
Texas
- Dallas Heart and Vascular Consultants, PADuncanville, Texas
- Texas Institute of Cardiology, PAMcKinney, Texas
- North Hills Family Medicine/North Hills Medical ResearchNorth Richland Hills, Texas
Utah
- Advanced Research InstituteOgden, Utah
Virginia
- Carient Heart & Vascular - ManassasManassas, Virginia
- Health Research of Hampton Roads, Inc.Newport News, Virginia
- National Clinical Research, IncRichmond, Virginia
Washington
- Eastside Research AssociatesRedmond, Washington
Timeline
Started enrolling: 2025-04-30. Expected completion: 2027-09. Last updated on ClinicalTrials.gov: 2026-05-12.
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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