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A Study to Learn How Safe and Tolerable Vonsetamig is in Adult Patients With Chronic Kidney Disease (CKD) Who Need Kidney Transplantation and Are Highly Sensitized to Human Leukocyte Antigen (HLA)
Sponsor: Regeneron Pharmaceuticals
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
Official title: 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
Key Details
Gender
All
Age Range
18 Years - 70 Years
Study Type
INTERVENTIONAL
Enrollment
56
Start Date
2022-08-02
Completion Date
2027-09-01
Last Updated
2026-02-12
Healthy Volunteers
No
Conditions
Interventions
Vonsetamig
Administered by intravenous (IV) infusion
Locations (10)
Cedars-Sinai Medical Center
Los Angeles, California, United States
University of California Irvine
Orange, California, United States
Connie Frank Transplant Center at UCSF
San Francisco, California, United States
Yale University of Medicine
New Haven, Connecticut, United States
Medstar Georgetown Transplant Institute - 2-PHC
Washington D.C., District of Columbia, United States
Comprehensive Transplant Center
Chicago, Illinois, United States
John Hopkins Hospital
Baltimore, Maryland, United States
University of Minnesota
Minneapolis, Minnesota, United States
New York University Langone Health
New York, New York, United States
Penn Transplant Institute
Philadelphia, Pennsylvania, United States