A study testing whether a GLP-1 medicine from AstraZeneca, semaglutide, can lower blood sugar and help with weight.
- Who can join
- Adults 18+, have type 2 diabetes, BMI 23+.
- What you take
- semaglutide, 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 1.8 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
Primary condition: Type 2 Diabetes Mellitus.
Full scientific study title: A Study to Find Out if the Study Drug Elecoglipron Helps Adults With Type 2 Diabetes Mellitus by Comparing it With Semaglutide, a Medicine A.
Who can join
Adults 18+, have type 2 diabetes, BMI 23+. A site coordinator confirms whether you qualify during a free screening visit. The exact medical requirements are below.
Full medical eligibility (for you and your doctor)verbatim from the registry
This is the exact wording from ClinicalTrials.gov, including clinical measures (lab values, imaging scores). Bring it to your doctor if any of it is unclear.
Key inclusion criteria
- Diagnosed with Type 2 Diabetes Mellitus (T2DM) for at least 90 days prior to screening
- T2DM inadequately managed with lifestyle management alone or on stable treatment with other background glucose-lowering medication(s)
- HbA1c value of >= 7% to <= 10.5% (53 to 91.3 mmol/mol)
- Increased risk of cardiovascular (CV) events defined by >=1 of: documented coronary heart disease, peripheral arterial disease, ischemic cerebrovascular disease, or heart failure (NYHA II-III); or >=2 CV risk factors
- Body mass index (BMI) of >= 23 kg/m2 at screening
Key exclusion criteria
- Type 1 Diabetes Mellitus (T1DM), secondary forms of diabetes (including congenital forms), or history of ketoacidosis or hyperosmolar coma
- Currently receiving or anticipated to receive, therapeutic intervention for diabetic retinopathy and/or macular edema
- Have had more than one episode of severe hypoglycemia within 180 days prior to screening or has a history of hypoglycemia unawareness or poor recognition of hypoglycemic symptoms
- Clinically significant condition affecting the upper Gastrointestinal (GI) tract or chronic use of any medication that affects gastric motility or gastric emptying
- History of acute or chronic pancreatitis
Where this study is enrolling
This trial has 41 sites across 23 states. Contact a site coordinator directly to start screening.
Alabama1 site
- Research SiteBirmingham, Alabama
Arizona3 sites
- Research SiteMesa, Arizona
- Research SitePhoenix, Arizona
- Research SiteTempe, Arizona
California5 sites
- Research SiteEncinitas, California
- Research SiteGarden Grove, California
- Research SiteLincoln, California
- Research SiteLoma Linda, California
- Research SitePomona, California
Florida4 sites
- Research SiteCrystal River, Florida
- Research SiteHollywood, Florida
- Research SiteJacksonville, Florida
- Research SiteLeesburg, Florida
Idaho1 site
- Research SiteIdaho Falls, Idaho
Illinois1 site
- Research SiteMelrose Park, Illinois
Iowa1 site
- Research SiteAmes, Iowa
Kansas1 site
- Research SiteWichita, Kansas
Kentucky1 site
- Research SiteBowling Green, Kentucky
Maryland1 site
- Research SiteRockville, Maryland
Michigan1 site
- Research SiteSouthfield, Michigan
Missouri2 sites
- Research SiteJefferson City, Missouri
- Research SiteKansas City, Missouri
Nebraska1 site
- Research SiteOmaha, Nebraska
Nevada2 sites
- Research SiteHenderson, Nevada
- Research SiteLas Vegas, Nevada
New Mexico1 site
- Research SiteAlbuquerque, New Mexico
North Carolina4 sites
- Research SiteDurham, North Carolina
- Research SiteMorehead City, North Carolina
- Research SiteStatesville, North Carolina
- Research SiteWilmington, North Carolina
Ohio1 site
- Research SiteColumbus, Ohio
Oklahoma1 site
- Research SiteYukon, Oklahoma
Texas2 sites
- Research SiteDallas, Texas
- Research SiteSugar Land, Texas
Utah2 sites
- Research SiteBountiful, Utah
- Research SiteSalt Lake City, Utah
Virginia2 sites
- Research SiteLeesburg, Virginia
- Research SiteNorfolk, Virginia
Washington2 sites
- Research SiteSeattle, Washington
- Research SiteSeattle, Washington
West Virginia1 site
- Research SiteMorgantown, West Virginia
Timeline
Started enrolling: 2026-07-06. Expected completion: 2028-05-23. Last updated on ClinicalTrials.gov: 2026-06-23.
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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