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Recruiting Phase 1 Interventional

Treatment of Antibody-Mediated Rejection (ABMR) With CarBel

ClinicalTrials.gov ID: NCT06918990

Public ClinicalTrials.gov record NCT06918990. 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 Sep 11, 2026, 5:41 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

Targeting the B Cell Response to Treat Antibody-Mediated Rejection With Carfilzomib and Belatacept (CarBel)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate the safety of carfilzomib and belatacept, administered with steroids and maintenance immunosuppression, in kidney transplant recipients with donor-specific antibody (DSA)-associated graft injury. Participants will be followed for 52 weeks after starting investigational therapy, including protocol biopsies at 3 months and 12 months after start of investigational therapy. The study will also assess changes in immune cell responses, blood and urine biomarkers, and biopsy-based pathomic features associated with antibody-mediated graft injury.

Study identification

NCT ID
NCT06918990
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 1
Enrollment
25 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
18 Years to 75 Years
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
May 26, 2026
Primary completion
Jun 29, 2027
Completion
Jun 29, 2027
Last update posted
Aug 9, 2026

2026 – 2027

United States locations

U.S. sites
11
U.S. states
9
U.S. cities
10
Facility City State ZIP Site status
University of Alabama Medical Center (Site # 71136) Birmingham Alabama 35294 Not yet recruiting
Mayo Clinic Arizona (Site # 71144) Phoenix Arizona 85054 Recruiting
UCLA Medical Center (Site #: 71123) Los Angeles California 90024 Not yet recruiting
Northwestern University, Feinberg School of Medicine (Site # 71110) Chicago Illinois 60611 Recruiting
Washington University (Site # 71157) St Louis Missouri 63110 Recruiting
NYU Langone Health (Site # 71177) New York New York 10016 Recruiting
Duke University (Site # 71139) Durham North Carolina 27710 Recruiting
Christ Hospital (Site # 71195) Cincinnati Ohio 45267 Not yet recruiting
University of Cincinnati (Site # 71118) Cincinnati Ohio 45267 Recruiting
Cleveland Clinic (Site # 71101) Cleveland Ohio 44195 Recruiting
University of Wisconsin Madison (Site # 71112) Madison Wisconsin 53726 Not yet recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06918990, 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 Aug 9, 2026 · Synced Sep 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06918990 live on ClinicalTrials.gov.

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