Condition: Kidney Transplant · Kidney Failure · End Stage Renal Failure on Dialysis · Sponsor: National Institute of Allergy and Infectious Diseases (NIAID)
This research study is for people who have been waiting for a kidney transplant for at least one year, and who have a cPRA of 99.5% or higher. Having a cPRA of 99.5% or higher means that your immune system would reject 99.5% of kidneys available for transplant. The study will test whether new products called Chimeric Antigen Receptor T Cells (CAR T Cells), when given with chemotherapy, is safe and will reduce cPRA. The main study will last up to 2 years: Participants will have up to 30 clinic or hospital visits over a one-year period. If a transplant takes place, there will be 9 more visits after transplant. Long term follow up is required by the Food and Drug Administration (FDA) for 15 years after receiving CAR T cell. The primary objective is to evaluate the safety and feasibility of administering CART BCMA + huCART-19 following lymphodepletion, including determination of optimal tolerated regimen (OTR) and/or recommended phase 2 regimen, according to the incidence of dose limiting toxicity (DLT) in highly sensitized patients awaiting kidney transplant.
This description comes directly from the study's public registry record.
Mary Kaminski, PA · 215-349-8334 · mary.kaminski@pennmedicine.upenn.edu
Always discuss trial participation with your own doctor first.
| Massachusetts General Hospital: Transplantation (Site #: 71107) | Boston, Massachusetts, United States | Recruiting |
| NYU Langone Health (Site #: 71177) | New York, New York, United States | Recruiting |
| University of Pennsylvania Medical Center (Site #: 71111) | Philadelphia, Pennsylvania, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06056102