Patient Guide: 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

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 70 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06340854
Status: ACTIVE_NOT_RECRUITING
Condition: Diabetes, Type 2
Phase: PHASE3

Where You Can Participate

This study is available at 70 locations across the country.

Top locations include:
  • • Hawthorne, California
  • • La Jolla, California
  • • Lincoln, California
  • • And 67 more locations

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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 - Join Clinical Trial NCTNCT06340854

How to Join This Clinical Trial - NCTNCT06340854

Learn how to participate in this PHASE3 trial studying an investigational therapy for Diabetes, Type 2. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Diabetes, Type 2. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Diabetes, Type 2
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT06340854 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 70 locations. Find a study site near you:

Clinical Research Site

Hawthorne, California 90250 - United States

Status: Contact for availability

Clinical Research Site

La Jolla, California 92037 - United States

Status: Contact for availability

Clinical Research Site

Lincoln, California 95648 - United States

Status: Contact for availability

Clinical Research Site

Fleming Island, Florida 32003 - United States

Status: Contact for availability

Clinical Research Site

Miramar, Florida 33027 - United States

Status: Contact for availability

Clinical Research Site

Roswell, Georgia 30076 - United States

Status: Contact for availability

Clinical Research Site

Topeka, Kansas 66606-2806 - United States

Status: Contact for availability

Clinical Research Site

Minneapolis, Minnesota 55416 - United States

Status: Contact for availability

Clinical Research Site

Jefferson City, Missouri 65109 - United States

Status: Contact for availability

Clinical Research Site

Omaha, Nebraska 68198-3020 - United States

Status: Contact for availability

And 60 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE3 clinical trial for Diabetes, Type 2:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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