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Completed Phase 3 Interventional

A Research Study to See How Much CagriSema Lowers Blood Sugar and Body Weight Compared to Placebo in People With Type 2 Diabetes Treated With Diet and Exercise

ClinicalTrials.gov ID: NCT06323174

Public ClinicalTrials.gov record NCT06323174. 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 May 20, 2026, 2:19 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) s.c. in Doses 2.4 mg/2.4 mg and 1.0 mg/1.0 mg Once Weekly Versus Placebo in Participants With Type 2 Diabetes Inadequately Controlled on Diet and Exercise

Study identification

NCT ID
NCT06323174
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
189 participants

Conditions and interventions

Interventions

  • Cagrilintide Drug
  • Placebo Drug
  • Semaglutide Drug

Drug

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
Mar 18, 2024
Primary completion
Sep 30, 2025
Completion
Dec 21, 2025
Last update posted
Apr 1, 2026

2024 – 2025

United States locations

U.S. sites
21
U.S. states
10
U.S. cities
21
Facility City State ZIP Site status
Nat Res Inst Huntington Park Huntington Park California 90255
Valley Clinical Trials, Inc. Northridge California 91325
Southern California Dermatology Santa Ana California 92701
Encore Medical Research LLC Hollywood Florida 33024
Headlands Research Orlando Orlando Florida 32819
Encore Medical Research of Weston Weston Florida 33331
Alliance for Multispec Res Newton Kansas 67114
Brigham & Women's Hospital Boston Massachusetts 02115
Arcturus HC PLC Troy Med Res Troy Michigan 48098
Southgate Medical Group, LLP West Seneca New York 14224
Summit Research Network Oregon Inc. Portland Oregon 97210
Holston Medical Group Kingsport Tennessee 37660
Amarillo Medical Specialists Amarillo Texas 79124
Elligo Clin Res Centre Austin Texas 78704
Headlands Research Brownsville Brownsville Texas 78526
Velocity Clinical Res-Dallas Dallas Texas 75230
Northeast Clinical Research of San Antonio San Antonio Texas 78233
Consano Clinical Research, LLC Shavano Park Texas 78231
Sugar Lakes Family Practice PA Sugar Land Texas 77479
Valley Diab. & Endo Comp Ctr Weslaco Texas 78596
TPMG Clinical Research Newport News Virginia 23606

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 29 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06323174, 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 Apr 1, 2026 · Synced May 20, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06323174 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →