A Dose Escalation and Proof-of-Concept Study of Vonsetamig (BCMA × CD3 Bispecific Antibody) for Desensitization of Chronic Kidney Disease Patients in Need of Kidney Transplantation Who Are Highly Sensitized to Human Leukocyte Antigen

Status: Recruiting
Location: See all (10) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1/Phase 2
SUMMARY

The purpose of this study is to determine whether vonsetamig will safely decrease anti-HLA antibodies to allow for kidney transplantation. Vonsetamig is being studied for treatment of patients in need of kidney transplantation who are highly sensitized to HLA. The study is looking at several other research questions, including: * Side effects that may be experienced from taking vonsetamig * How vonsetamig works in the body * How much vonsetamig is present in the blood * If vonsetamig works to lower levels of antibodies to HLA

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: f
View:

• Has Chronic Kidney Disease (CKD) requiring hemodialysis, and awaiting kidney transplant on the United Network for Organ Sharing (UNOS), with a cPRA ≥99.9%, or those with a cPRA \>98% (98.1% to 99.8%) who have spent 5 years or longer on the waitlist, as defined in the protocol

• Adequate hematologic and adequate hepatic function as defined in the protocol

• Willing and able to comply with clinic visits and study-related procedures

Locations
United States
California
Cedars-Sinai Medical Center
RECRUITING
Los Angeles
University of California Irvine
RECRUITING
Orange
Connie Frank Transplant Center at UCSF
RECRUITING
San Francisco
Connecticut
Yale University of Medicine
RECRUITING
New Haven
Washington, D.c.
Medstar Georgetown Transplant Institute - 2-PHC
RECRUITING
Washington D.c.
Illinois
Comprehensive Transplant Center
RECRUITING
Chicago
Maryland
John Hopkins Hospital
RECRUITING
Baltimore
Minnesota
University of Minnesota
RECRUITING
Minneapolis
New York
New York University Langone Health
RECRUITING
New York
Pennsylvania
Penn Transplant Institute
RECRUITING
Philadelphia
Contact Information
Primary
Clinical Trials Administrator
clinicaltrials@regeneron.com
844-734-6643
Time Frame
Start Date: 2022-08-02
Estimated Completion Date: 2026-12-12
Participants
Target number of participants: 56
Treatments
Experimental: Vonsetamig
Related Therapeutic Areas
Sponsors
Leads: Regeneron Pharmaceuticals

This content was sourced from clinicaltrials.gov