A study testing whether a GLP-1 medicine from Novo Nordisk, semaglutide, can lower blood sugar and help with weight.

Who can join
Adults 18 to 75, have type 2 diabetes.
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 study runs about 17 months.
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.
Phase Phase 2Sponsor Novo Nordisk A/SDrug semaglutideClass GLP-1 RASites 25 USEnrollment target 300

What this study is for

Primary condition: Diabetes Mellitus, Type 2.

For trial evidence and insurance approval criteria for this condition, see the Type 2 diabetes condition guide.

Full scientific study title: A Research Study Comparing How Well Different Doses of the Medicine UBT251 Lower Blood Sugar in People With Type 2 Diabetes.

Who can join

Age18 to 75SexAny

Adults 18 to 75, have type 2 diabetes. 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

  • Male or female (sex assigned at birth, inclusive of all gender identities).
  • Age 18-75 years (both inclusive) at the time of signing the informed consent.
  • Diagnosed with type 2 diabetes greater than or equal to (>=) 180 days before screening.
  • Stable daily dose(s) >= 90 days before screening of the following antidiabetic drug(s) or combination regimen(s) at effective or maximum tolerated dose as judged by the investigator:
  • HbA1c of 7.0-10.5 percent (%) (53-91 millimoles per mole (mmol/mol)) (both inclusive) as assessed by central laboratory at screening.

Key exclusion criteria

  • Treatment with any medication (prescription or over-the counter) or alternative remedies for the indication of diabetes or obesity other than stated in the inclusion criteria within 90 days before screening. However, short term insulin treatment for a maximum of 14 consecutive days and prior insulin treatment for gestational diabetes are allowed.
  • Uncontrolled and potentially unstable diabetic retinopathy or maculopathy. Verified by an eye examination performed within 90 days before screening or in the period between screening and randomisation. Pharmacological pupil-dilation is a requirement unless using a digital fundus photography camera specified for non-dilated examination.
  • Known hypoglycaemic unawareness as indicated by the investigator according to Clarke's questionnaire, question 8.

Where this study is enrolling

This trial has 25 sites across 14 states. Contact a site coordinator directly to start screening.

Alabama1 site
  • Flourish Research
    Birmingham, Alabama
California4 sites
  • Ark Clinical Research
    Fountain Valley, California
  • Ark Clinical Research
    Long Beach, California
  • Los Angeles Institute for Metabolic Research
    Los Angeles, California
  • Catalina Research Institute, LLC
    Montclair, California
Florida3 sites
  • Encore Medical Research LLC
    Hollywood, Florida
  • South Broward Research LLC
    Miramar, Florida
  • Encore Medical Research of Weston
    Weston, Florida
Indiana1 site
  • Midwest Inst For Clin Res
    Indianapolis, Indiana
Kansas1 site
  • Cotton O'Neil Diabetes & Endocrinology
    Topeka, Kansas
Maryland1 site
  • MD Medical Research
    Oxon Hill, Maryland
North Carolina2 sites
  • PharmQuest
    Greensboro, North Carolina
  • KDCILM, LLC & Accellacare US, Inc.
    Wilmington, North Carolina
North Dakota1 site
  • Plains Clinical Research Center, LLC_Fargo
    Fargo, North Dakota
Pennsylvania1 site
  • Preferred Primary Care Physicians, Inc.
    Uniontown, Pennsylvania
South Carolina1 site
  • Monroe Biomedical Research, LLC
    North Charleston, South Carolina
Tennessee1 site
  • LifeDoc Health
    Memphis, Tennessee
Texas6 sites
  • IMA Clinical Research
    Austin, Texas
  • Private Practice - Dr. Laila A. Hassan
    Houston, Texas
  • Radiance Clinical Research
    Lampasas, Texas
  • Quality Research Inc
    San Antonio, Texas
  • Tekton Research Inc
    San Antonio, Texas
  • Consano Clin Res-Shavano Park
    Shavano Park, Texas
Utah1 site
  • Chrysalis Clinical Research
    St. George, Utah
Washington1 site
  • The Vancouver Clinic
    Vancouver, Washington

Timeline

Started enrolling: 2026-06-22. Expected completion: 2027-11-15. Last updated on ClinicalTrials.gov: 2026-06-25.

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:

View on ClinicalTrials.gov →

Back to the full directory → or take the matching quiz if you want clinical trials filtered to your conditions and location.

Why you can trust GLP ChartSame scoring framework applied to every program. No paid placements. We never remove unfavorable information at an advertiser's request. Pricing is pulled from each program's public-facing page every Monday.