The purpose of this study is to evaluate the safety and the efficacy of SMART101 (Human T Lymphoid Progenitor (HTLP)) injection to accelerate immune reconstitution after T cell depleted allogeneic hematopoietic stem cell transplantation (HSCT) in adult and pediatric patients with hematological malignancies.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
36
Injection of T cell progenitors at \[Day 4-Day 10\] after T cell depleted allogeneic HSCT
Memorial Sloan Kettering Cancer Center (MSKCC)
New York, New York, United States
RECRUITINGCumulative incidence of grade III-IV GvHD
to evaluate the safety profile of the study drug
Time frame: 100 days post-HSCT
Occurrence of adverse events related to SMART101
Number of adverse events and serious adverse events related to SMART101 tabulated for each dose and by age group to evaluate the safety profile of the study drug
Time frame: 100 days post-HSCT
CD4+ T cell count
to evaluate the efficacy of the study drug
Time frame: 100 days post-HSCT
T cell immune reconstitution
Time course of the T cell immune reconstitution, with a focus on naive CD4+ cells and total CD8+ cells
Time frame: up to Month 12 post-HSCT
Cumulative incidence of infections
Time frame: Day 90, and Months 6, 12 and 24 post-HSCT
Non-relapse mortality (NRM)
Time frame: Day 90, and Months 6, 12 and 24 post-HSCT
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