A study testing whether a GLP-1 medicine, semaglutide, can help people lower blood sugar.

Recruiting now. Registry record last updated March 4, 2026.

Who can join
Adults 18 to 49, have type 1 diabetes, BMI 20+.
What you take
semaglutide, given as part of the study. Check ClinicalTrials.gov for this trial's study groups, including any placebo or comparison medicine.
How long it lasts
The full study runs about 4.5 years; your own time in it is usually shorter.
What you get
Many clinical trials pay for the study medication and the study visits. Some also pay for travel. Ask the study team what this one covers before you sign the consent form.
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Phase Phase 3Sponsor University of Colorado, DenverDrug semaglutideClass GLP-1 RASites 2 USEnrollment target 60

What this study is for

Primary condition: Diabetes Mellitus, Type 1.

Full scientific study title: Type 1 Diabetes Impacts of Semaglutide on Cardiovascular Outcomes.

Who can join

Age18 to 49SexAnyBMI20 to 45

Adults 18 to 49, have type 1 diabetes, BMI 20+. 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

  • Age 18-49 years
  • 1\) T1D diagnosis defined as positive T1D-associated antibody(ies) or 2) a clinical diagnosis of T1D plus insulin requirement since diagnosis
  • Insulin pump or automated insulin delivery systems
  • Estimated glomerular filtration rate (eGFR) ≥ 45 ml/min/1.73m2
  • Stable doses of drugs altering cardiovascular and renal function (e.g., Angiotensin-Converting Enzyme Inhibitor (ACEi), Angiotensin Receptor Blocker (ARB), statins, diuretics)

Key exclusion criteria

  • HbA1c \>9%, recent diabetic ketoacidosis (DKA) or hospitalization
  • Major congenital heart disease, anemia, severe non-proliferative retinopathy, proliferative retinopathy
  • History/family history of medullary thyroid carcinoma, multiple endocrine neoplasia type 2 (MEN2), pancreatitis
  • Current/planned pregnancy or nursing
  • Uncontrolled thyroid disease or hypertension (HTN) (≥ 160/100 mm Hg despite optimal therapy)

Where this trial is enrolling

This trial has 2 sites across 2 states. Contact a site coordinator directly to start screening.

Colorado1 site
Washington1 site
  • University of Washington Medicine Diabetes Institute (UWMDI)
    Seattle, Washington
    Amanda Bard504-521-7822abard@uw.edu

Timeline

Started enrolling: June 21, 2023. Expected completion: December 1, 2027. Last updated on ClinicalTrials.gov: March 4, 2026.

Official source

Every Monday we check this trial against ClinicalTrials.gov, the federal registry for clinical research. Last checked August 21, 2026. Confirm the current status there before you contact a site:

View on ClinicalTrials.gov →

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