drugset / Trial / NCT01807611

Haploidentical Donor Hematopoietic Progenitor Cell and NK Cell Transplantation for Hematologic Malignancy

NCT01807611

NaSingle-groupOpen-labelTreatment

Summary

In this study, participants with high-risk hematologic malignancies undergoing hematopoietic cell transplantation (HCT), who do not have a suitable human leukocyte antigen (HLA) matched related/sibling donor (MSD) or matched unrelated donor (MUD) identified, will receive a haploidentical donor HCT with additional natural killer (NK) cells. The investigators anticipate enrollment of 75 donors and 75 recipients. PRIMARY OBJECTIVE: * To estimate the rate of successful engraftment at day +42 post-transplant in patients who receive haploidentical donor stem cell plus NK cell transplantation with TLI based conditioning regimen for high risk hematologic malignancy. SECONDARY OBJECTIVES: * Estimate the incidence of malignant relapse, event-free survival, and overall survival at one-year post-transplantation. * Estimate incidence and severity of acute and chronic (GVHD). * Estimate the rate of transplant related mortality (TRM) in the first 100 days after transplantation.

Timeline

Start
2013-05-16
Primary completion
2021-08-27
Completion
2021-09-27

Drugs

EvaluationDrugModalityDoseRoute
Subject HPC,A Infusion Cell therapy
Subject TC-NK Infusion Cell therapy
Background 2-MERCAPTOETHANESULFONIC ACID Small molecule 25 % Intravenous
Background Cyclophosphamide Other / unclassified Intravenous
Background Fludarabine Small molecule Intravenous
Background G-CSF Unknown Subcutaneous
Background Melphalan Small molecule Intravenous
Background Mycophenolate Mofetil Small molecule Intravenous
Background Thiotepa Other / unclassified Intravenous

Indications