Condition: Epstein-Barr Virus · Cytomegalovirus Infections · Adenovirus · Sponsor: Columbia University
The primary objective is to determine the safety and feasibility of administering R-MVST cells to patients with refractory viral reactivation and/or symptomatic disease caused by Epstein Barr Virus (EBV), cytomegalovirus (CMV), adenovirus (ADV) or BK virus. R-MVST cells will be generated on-demand from the closest partially human leukocyte antigen (HLA)-matched (minimum haploidentical) healthy donors or from the original allo-transplant donor if available. The investigator will closely monitor the recipients for potential toxicities including graft-versus-host disease (GVHD) post-infusion. Secondary objectives are to determine the effect of R-MVST infusion on viral load, possible recovery of antiviral immunity post-infusion and for evidence of clinical responses and overall survival. Recipients will be monitored for secondary graft failure at day 28 post R-MVST infusion.
This description comes directly from the study's public registry record.
Prakash Satwani, MD · 212-305-0223 · ps2087@cumc.columbia.edu
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| Columbia University Medical Center / New-York Presbyterian | New York, New York, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06926894