Not yet recruiting · NCT07357740

A study testing whether a study medicine from Novo Nordisk, cagrisema, can lower blood sugar and help with weight.

Who can join
Adults 18 to 64, have type 2 diabetes, BMI 25+.
What you take
cagrisema, 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 14 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 cagrisemaClass OtherSites 21 USEnrollment target 400

What this study is for

Full study title: A Research Study to Compare Two Different Versions of Injectable CagriSema in People With Type 2 Diabetes.

Primary condition: Diabetes Mellitus, Type 2.

Who can join, in detail

Age 18 to 64
Sex All
BMI 25 to 39.9

Key inclusion criteria

  • Male or female (sex assigned at birth, inclusive of all gender identities).
  • Age 18-64 years (both inclusive) at the time of signing the informed consent.
  • Diagnosed with type 2 diabetes mellitus greater than or equal to (>=) 180 days before screening.
  • Glycated haemoglobin (HbA1c) 7.0-10.5 percent (%) (53-91 [millimoles per mole] mmol/mol) (both inclusive) as determined by the central laboratory at screening.
  • Stable daily dose >= 90 days before screening of metformin at effective or maximum tolerated dose as judged by the investigator.

Key exclusion criteria

  • Renal impairment with estimated Glomerular Filtration Rate (eGFR) < 30 millilitre per minute per 1.73 square metre (mL/min/1.73 m^2) as determined by the central laboratory at screening.
  • Treatment with any anti-diabetic or anti-obesity medication (irrespective of indication) other than stated in the inclusion criteria within 90 days before screening.
  • 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.
  • Previous exposure to CagriSema in a clinical study.

Where this study is enrolling

This trial has 21 US sites across 10 states. Contact the site coordinator directly to start the screening process.

Arkansas

  • Arkansas Clinical Research
    Little Rock, Arkansas

California

  • Paradigm Clinical Research
    San Diego, California
  • Encompass Clinical Research_Spring Valley
    Spring Valley, California
  • Diablo Clinical Research, Inc.
    Walnut Creek, California

Florida

  • Future Medical Research
    Longwood, Florida
  • New Horizon Research Center
    Miami, Florida
  • Clinical Site Partners Kendall Flourish Research
    Miami, Florida
  • West Orange Endocrinology
    Ocoee, Florida
  • Center for Diab,Obes & Metab
    Pembroke Pines, Florida
  • American Research Centers of Florida
    Pembroke Pines, Florida

Georgia

  • Hope Clin Res & Wellness
    Conyers, Georgia

Illinois

  • Elevate Clinical Research
    Gurnee, Illinois
  • Accellacare of Duly Oak Lawn
    Oak Lawn, Illinois

North Carolina

  • KDCILM, LLC & Accellacare US, Inc.
    Wilmington, North Carolina

Ohio

  • Advanced Medical Research - Maumee
    Maumee, Ohio

Rhode Island

  • Clinical Res Collaborative
    Cumberland, Rhode Island

Tennessee

  • Clinical Research Associates
    Nashville, Tennessee

Texas

  • The Endocrine Center
    Houston, Texas
  • Radiance Clinical Research
    Lampasas, Texas
  • Quality Research Inc
    San Antonio, Texas
  • Medrasa Clinical Research
    Sherman, Texas

Timeline

Started enrolling: 2026-08-27. Expected completion: 2027-10-13. Last updated on ClinicalTrials.gov: 2026-03-30.

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 →

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