CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 82 enrolled
Drug / intervention
Fludarabine +10 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01807611
NCT01807611Phase 2Completed

Haploidentical Donor Hematopoietic Progenitor Cell and Natural Killer Cell Transplantation With a TLI Based Conditioning Regimen in Patients With Hematologic Malignancies

St. Jude Children's Research Hospital·interventional·Posted Mar 8, 2013·Updated Oct 31, 2022

In Brief

A Phase 2 clinical trial evaluating Total Lymphoid Irradiation, Fludarabine, and 9 other interventions for Leukemia and Lymphoma. Completed, enrolled 82 participants across 1 site.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsLeukemia, Lymphoma
CountriesUnited States
CollaboratorsAssisi Foundation

Timeline

Phase 2CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedMar 8, 2013
Enrollment StartMay 16, 2013
Primary CompletionAug 27, 2021
Study CompletionSep 27, 2021
TodayJul 2, 2026
Enrollment to primary: 8.3 yearsPosted 13.3 years ago

Interventions

Total Lymphoid Irradiationradiation

Participants receive total lymphoid irradiation over four doses.

Fludarabinedrug

Given IV.

Cyclophosphamidedrug

Given IV.

Thiotepadrug

Given IV.

Melphalandrug

Given IV.

HPC,A Infusionbiological

Participants received infusions of HPC,A (CD34+ selected) and HPC,A (CD45RA depleted).

TC-NK Infusionbiological

Participants receive infusions of TC-NK.

G-CSFbiological

Participants receive G-CSF subcutaneously or intravenously. Donors receive G-CSF subcutaneously during cell mobilization.

Mesnadrug

Mesna is generally dosed at approximately 25% of the cyclophosphamide dose. It is generally given intravenously prior to and again at 3, 6 and 9 hours following each dose of cyclophosphamide.

CliniMACSdevice

The mechanism of action of the CliniMACS Cell Selection System is based on magnetic-activated cell sorting (MACS). The CliniMACS device is a powerful tool for the isolation of many cell types from heterogeneous cell mixtures, (e.g. apheresis products). These can then be separated in a magnetic field using an immunomagnetic label specific for the cell type of interest, such as CD3+ human T cells.

Mycophenolate mofetildrug

Given intravenously or orally.