Enrolling now · NCT06717698

A study testing whether a GLP-1 medicine from Novo Nordisk, semaglutide, can protect the kidneys.

What this means for you

Who can join
Adults 18+, have chronic kidney disease, BMI 27+.
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.
Phase Phase 2Sponsor Novo Nordisk A/SDrug semaglutideClass GLP-1 RASites 18 USEnrollment target 465

What this study is for

Primary condition: Chronic Kidney Disease.

Full scientific study title: A Research Study Comparing How Well Different Doses of the Medicine NNC0519-0130 Can Reduce Kidney Damage in People Living With Chronic Kidn.

Who can join

Age18 and upSexAnyBMI27 or higher

Adults 18+, have chronic kidney disease, BMI 27+. 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

  • Female of non-childbearing potential, or male.
  • For US only: Female of childbearing potential using highly effective non-systemic methods of contraception with low user-dependency at least 2 months prior to screening and willingness to continue using it through-out the study, or male.
  • Age 18 years or above at the time of signing the informed consent.
  • Diagnosed with type 2 diabetes mellitus greater than or equal to (>=) 180 days before screening, or not diagnosed with type 2 diabetes mellitus.
  • HbA1c of 6.5 percentage (%)-10.5 percentage (%) [48 - 91 millimoles per mole (mmol/mol)] (both inclusive) if diagnosed with type 2 diabetes mellitus, or HbA1c of less than (<)6.5 percentage (%) [<48 mmol/mol] if not diagnosed with type 2 diabetes mellitus.

Key exclusion criteria

  • Female who is pregnant, breast-feeding or intends to become pregnant or is of childbearing potential and not using highly effective non-systemic contraception with low user-dependency.
  • Lupus nephritis or antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis.
  • Receiving immunosuppressive therapy for primary or secondary renal disease within 6 months prior to screening.
  • Use of any glucagon-like peptide-1 (GLP-1) RA (including medication with GLP-1 RA activity, e.g., GIP/GLP-1 RA) within 90 days prior to screening.
  • Myocardial infarction, stroke, transient ischaemic attack, or hospitalization for unstable angina pectoris within 180 days before screening.

Where this study is enrolling

This trial has 18 sites across 11 states. Contact a site coordinator directly to start screening.

California2 sites
  • N America Res Inst - San Dimas
    San Dimas, California
  • NorCal Endocrinology and Internal Medicine
    San Ramon, California
Colorado1 site
  • Rocky Mount Reg VA Med-DN
    Aurora, Colorado
Florida4 sites
  • Northeast Research Institute
    Fleming Island, Florida
  • Encore Medical Research LLC
    Hollywood, Florida
  • Northeast Research Institute
    Saint Augustine, Florida
  • Clinical Research of Cent FL
    Winter Haven, Florida
Illinois1 site
  • Endeavor Health
    Skokie, Illinois
Indiana1 site
  • Velocity Clin. Res Valparaiso
    Valparaiso, Indiana
Michigan1 site
  • Elite Research Center
    Flint, Michigan
Missouri1 site
  • Clinical Research Consultants
    Kansas City, Missouri
New York1 site
  • Albany Medical College
    Albany, New York
North Carolina2 sites
  • Carteret Medical Group
    Morehead City, North Carolina
  • Brookview Hills Research Associates, LLC
    Winston-Salem, North Carolina
Texas3 sites
  • Davita Clinical Research
    El Paso, Texas
  • Clinical Advancement Center
    San Antonio, Texas
  • Tekton Research
    San Antonio, Texas
Washington1 site
  • Providence Medical Research Center
    Spokane, Washington

Timeline

Started enrolling: 2024-12-02. Expected completion: 2026-09-17. Last updated on ClinicalTrials.gov: 2026-03-11.

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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