Patient Guide: A Study to Evaluate the Benefits and Risks of Conversion of Existing Adolescent Kidney Transplant Recipients Aged 12 to <18 Years to a Belatacept-based Immunosuppressive Regimen as Compared to Continuation of a Calcineurin Inhibitor-based Regimen, and Their Adherence to Immunosuppressive Medications

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 37 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04877288
Status: 🟢 Enrolling Now
Condition: Renal Allograft Recipients
Phase: PHASE3

Where You Can Participate

This study is available at 37 locations across the country.

Top locations include:
  • • Birmingham, Alabama
  • • Los Angeles, California
  • • Washington, District of Columbia
  • • And 34 more locations

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A Study to Evaluate the Benefits and Risks of Conversion of Existing Adolescent Kidney Transplant Recipients Aged 12 to <18 Years to a Belatacept-based Immunosuppressive Regimen as Compared to Continuation of a Calcineurin Inhibitor-based Regimen, and Their Adherence to Immunosuppressive Medications - Join Clinical Trial NCTNCT04877288

How to Join This Clinical Trial - NCTNCT04877288

Learn how to participate in this PHASE3 trial studying an investigational therapy for Renal Allograft Recipients. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Renal Allograft Recipients
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT04877288 - 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 37 locations. Find a study site near you:

Clinical Research Site

Birmingham, Alabama 35233 - United States

Status: WITHDRAWN

Clinical Research Site

Los Angeles, California 90095 - United States

Status: WITHDRAWN

Clinical Research Site

Washington, District of Columbia 20010 - United States

Status: WITHDRAWN

Clinical Research Site

Hollywood, Florida 33021 - United States

Status: WITHDRAWN

Clinical Research Site

Miami, Florida 33136 - United States

Status: WITHDRAWN

Clinical Research Site

Atlanta, Georgia 30322 - United States

Status: WITHDRAWN

Clinical Research Site

Chicago, Illinois 60611 - United States

Status: WITHDRAWN

Clinical Research Site

Baltimore, Maryland 21287 - United States

Status: WITHDRAWN

Clinical Research Site

Boston, Massachusetts 02115 - United States

Status: WITHDRAWN

Clinical Research Site

Saint Louis, Missouri 63110 - United States

Status: WITHDRAWN

And 27 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 Renal Allograft Recipients:

  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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