RecruitingNCT05106387

An Observational Extension Study for Adult Patients Treated in Study R5459-RT-1944 Who Receive a Kidney Transplant

A Noninterventional Extension Study for Patients Treated in Study R5459-RT-1944 With Vonsetamig (BCMA x CD3 Bispecific Antibody) Who Receive a Kidney Transplant


Sponsor

Regeneron Pharmaceuticals

Enrollment

20 participants

Start Date

Oct 19, 2023

Study Type

OBSERVATIONAL

Conditions

Summary

The main purpose of this study is to continue to see how vonsetamig works in the body and to monitor the outcomes after kidney transplant for participants previously treated in the R5459-RT-1944 study (NCT05092347). No study drug will be given during this study.


Eligibility

Min Age: 18 YearsMax Age: 70 Years

Inclusion Criteria4

  • Received at least 1 dose of treatment with vonsetamig in study R5459-RT-1944 \[NCT05092347\].
  • Received after acceptable crossmatching, a kidney transplant while enrolled in study R5459-RT-1944
  • Willing and able to comply with clinic visits and study-related procedures
  • Provide informed consent signed by study patient or legally acceptable representative

Interventions

DRUGNoninterventional

No investigational treatment will be given in this noninterventional extension study


Locations(9)

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

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

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT05106387


Related Trials