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Completed Phase 3 Interventional

A Research Study to See How Switching From a Daily Basal Insulin to a New Weekly Insulin, Insulin Icodec, Helps in Reducing the Blood Sugar Compared to Daily Insulin Glargine in Adults With Type 2 Diabetes

ClinicalTrials.gov ID: NCT06340854

Public ClinicalTrials.gov record NCT06340854. 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 5, 2026, 5:39 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

A Study to Evaluate the Efficacy and Safety of Once-weekly Insulin Icodec When Switching From Daily Basal Insulins Compared to Once-daily Insulin Glargine U100 in Adults With Type 2 Diabetes

Study identification

NCT ID
NCT06340854
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
429 participants

Conditions and interventions

Interventions

  • Insulin glargine Drug
  • Insulin icodec 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
Apr 18, 2024
Primary completion
May 7, 2025
Completion
Jun 12, 2025
Last update posted
Apr 8, 2026

2024 – 2025

United States locations

U.S. sites
21
U.S. states
14
U.S. cities
20
Facility City State ZIP Site status
Advanced Investigative Medicine, Inc. Hawthorne California 90250
Scripps Whittier Diabetes Inst La Jolla California 92037
Clinical Trials Research Lincoln California 95648
Northeast Research Institute of Florida Fleming Island Florida 32003
South Broward Research LLC Miramar Florida 33027
Endo Res Solutions Inc Roswell Georgia 30076
Cotton-Oneill Diabetes and End Topeka Kansas 66606-2806
International Diabetes Center Minneapolis Minnesota 55416
Jefferson City Medical Group, PC Jefferson City Missouri 65109
Univ of Nebraska Medical CTR Omaha Nebraska 68198-3020
Palm Research Center Inc-Vegas Las Vegas Nevada 89148
Southern NH Diabetes and Endo_Nashua Nashua New Hampshire 03060
PharmQuest Life Sciences LLC Greensboro North Carolina 27408
Accellacare Wilmington Wilmington North Carolina 28401
Trial Management Associates Myrtle Beach South Carolina 29572
Amarillo Medical Specialists Amarillo Texas 79124
Velocity Clinical Res-Dallas Dallas Texas 75230
Victorium Clinical Research Houston Texas 77024
PlanIt Research, PLLC Houston Texas 77079
Chrysalis Clinical Research St. George Utah 84790
Rainier Clin Res Ctr Inc Renton Washington 98057

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 51 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06340854, 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 8, 2026 · Synced May 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06340854 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →