Patient Guide: A Research Study to See How Well New Weekly Medicine IcoSema, Which is a Combination of Insulin Icodec and Semaglutide, Controls Blood Sugar Levels in People With Type 2 Diabetes (T2D), Compared to Daily Insulin Glargine (COMBINE 4)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 90 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06269107
Status: ACTIVE_NOT_RECRUITING
Condition: Type 2 Diabetes
Phase: PHASE3

Where You Can Participate

This study is available at 90 locations across the country.

Top locations include:
  • • La Jolla, California
  • • Lancaster, California
  • • Palm Springs, California
  • • And 87 more locations

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A Research Study to See How Well New Weekly Medicine IcoSema, Which is a Combination of Insulin Icodec and Semaglutide, Controls Blood Sugar Levels in People With Type 2 Diabetes (T2D), Compared to Daily Insulin Glargine (COMBINE 4) - Join Clinical Trial NCTNCT06269107

How to Join This Clinical Trial - NCTNCT06269107

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

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Type 2 Diabetes
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT06269107 - 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 90 locations. Find a study site near you:

Clinical Research Site

La Jolla, California 92037 - United States

Status: Contact for availability

Clinical Research Site

Lancaster, California 93534 - United States

Status: Contact for availability

Clinical Research Site

Palm Springs, California 92262 - United States

Status: Contact for availability

Clinical Research Site

Sacramento, California 95821 - United States

Status: Contact for availability

Clinical Research Site

Fleming Island, Florida 32003 - United States

Status: Contact for availability

Clinical Research Site

Winter Haven, Florida 33880 - United States

Status: Contact for availability

Clinical Research Site

Atlanta, Georgia 30318 - United States

Status: Contact for availability

Clinical Research Site

Blackfoot, Idaho 83221 - United States

Status: Contact for availability

Clinical Research Site

Chicago, Illinois 60607 - United States

Status: Contact for availability

Clinical Research Site

Skokie, Illinois 60077 - United States

Status: Contact for availability

And 80 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 Type 2 Diabetes:

  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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