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Completed Phase 2 Interventional

A Research Study to See if Kidney Damage in People With Chronic Kidney Disease and Type 2 Diabetes Living With Overweight or Obesity Can be Reduced by CagriSema Compared to Semaglutide, Cagrilintide and Placebo

ClinicalTrials.gov ID: NCT06131372

Public ClinicalTrials.gov record NCT06131372. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 28, 2026, 3:30 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Efficacy and Safety of Co-administered Cagrilintide and Semaglutide (CagriSema 2.4 mg/2.4 mg) Once Weekly Versus Semaglutide 2.4 mg, Cagrilintide 2.4 mg and Placebo in People With Chronic Kidney Disease and Type 2 Diabetes Living With Overweight or Obesity

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study will look if CagriSema can lower kidney damage in people with chronic kidney disease (CKD), type 2 diabetes (T2D) and overweight or obesity. CagriSema is a new investigational medicine. CagriSema cannot yet be prescribed by doctors. The study will compare CagriSema to the 2 medicines semaglutide and cagrilintide, when they are taken alone. It will also compare CagriSema to a "dummy" medicine (also called placebo) without any active ingredient. Participant will either get CagriSema, semaglutide, cagrilintide or placebo. Which treatment participant will get is decided by chance (like flipping a coin). Study doctor will not know which of the study medicines participant will get. For each participant, the study will last for about 35 weeks.

Study identification

NCT ID
NCT06131372
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
626 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 1, 2024 (Actual)
Primary completion
Sep 24, 2025 (Actual)
Completion
Nov 6, 2025 (Actual)
Last update posted
Sep 24, 2026

2024 – 2025

United States locations

U.S. sites
25
U.S. states
12
U.S. cities
25
Facility City State ZIP Site status
John Muir Physicians Network Concord California 94520 —
Valley Research Fresno California 93720 —
Desert Oasis Hlthcr Med Group Palm Springs California 92262 —
North America Research Institute San Dimas California 91773 —
NorCal Endocrinology and Internal Medicine San Ramon California 94583 —
Northeast Research Institute Fleming Island Florida 32003 —
Life Spring Research Foundation LLC Miami Florida 33130 —
Advent Health Translational Research Institute Orlando Florida 32804 —
Velocity Clin. Res Valparaiso Valparaiso Indiana 46383 —
Elite Research Center Flint Michigan 48532 —
Univ. of Nebraska Medical Center_Omaha Omaha Nebraska 68198 —
Albany Medical College Albany New York 12203 —
NYU Langone Nephrology Associates Mineola New York 11501 —
New York University Grossman School of Medicine New York New York 10016 —
Southgate Medical Group, LLP West Seneca New York 14224 —
Carteret Medical Group Morehead City North Carolina 28557 —
Eastern Nephrology Associates, PLLC New Bern North Carolina 28562 —
Brookview Hills Research Associates, LLC Winston-Salem North Carolina 27103 —
Ohio- Advanced Medical Research Maumee Ohio 43537 —
Heritage Valley Multispeciality Group Inc Beaver Pennsylvania 15009 —
Main Street Physician's Care Little River South Carolina 29566 —
Osvaldo A. Brusco MD Corpus Christi Texas 78414 —
Southwest Houston Research Ltd Houston Texas 77099 —
Clinical Advancement Center San Antonio Texas 78212 —
Clinical Investigation Specialists Inc, Kenosha Kenosha Wisconsin 53144 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 104 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06131372, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 24, 2026 · Synced Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06131372 live on ClinicalTrials.gov.

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