An interventional study of peripheral blood lymphocytes and CIK cell in B-cell Acute Lymphoblastic Leukemia, Acute Lymphoblastic Leukemia, in Relapse and Refractory Acute Lymphoid Leukemia, sponsored by Beijing GoBroad Hospital. Recruiting at 1 site in China. Open to participants aged 1 Year to 39 Years. Per ClinicalTrials.gov, last updated 2026-02-25.
Sponsored by Beijing GoBroad Hospital · Not applicable, Interventional, and Treatment
This is a single-center, double-blind, randomized trial. Patients with relapsed or refractory acute B-lymphoblastic leukemia(r/r B-ALL) experiencing early functional exhaustion of CAR-T cells will be randomly allocated into three groups: the control cell group, the CIK treatment group, and the messenger RNA(mRNA)-CIK treatment group. The primary objective of the study is to evaluate the prognostic impact of CIK cell therapy on the early functional exhaustion of CAR-T cells in children and adolescent and young adult (AYA) with r/r B-ALL. The primary endpoint of the study is the event-free survival rate of these patient in the CIK cell therapy group.A total number of 213 subjects will be enrolled.
392 studies on the registry are indexed under Burkitt Lymphoma; 114 are open to participants now.
This study's planned enrollment of 213 is above the median of 41 across 354 interventional studies indexed under Burkitt Lymphoma.
Browse Burkitt Lymphoma studies →Beijing GoBroad Hospital is the lead sponsor of 35 studies on the registry; 35 are open to participants now.
Counted across the registry records on this site, refreshed daily.
A patient must meet all of the following to be enrolled:
Exclusion Criteria:
A patient with at least one of the following conditions will be excluded:
Drug: peripheral blood lymphocytes
Drug: CIK cell
autologous or allogeneic peripheral blood lymphocytes
autologous or allogeneic cytokine-induced killer (CIK) cells
Event-free survival(EFS) in CIK infusion group
EFS is defined as the time from CIK-cell infusion to the earliest relapse, death from any cause, or treatment failure
Time frame: 2-year EFS rate
Progression-free survival(PFS) in CIK infusion group
PFS is defined as the time from CIK-cell infusion until objective tumor progression or death depending on study protocol
Time frame: 2-year PFS rate
Duration of response(DOR) in CIK infusion group
DOR is defined as the time interval from the earliest qualifying minimal residual disease-negative response \[i.e. complete remission(CR),complete remission with partial hematological recovery(CRh), complete remission with incomplete hematological recovery(CRi), morphologic leukemia-free state(MLFS), or aplastic marrow (patients with blood and bone marrow disease), central nervous system(CNS) remission (patients with CNS disease) and complete resolution of the lymphomatous enlargement by CT or positron emission tomography(PET)-CT negative (for patients with a previous positive PET-CT) (patients with lymphomatous extramedullary disease)\] to the date of relapse or death from any cause.
Time frame: from enrollment to the end of treatment at 15 years
Overall survival(OS) in CIK infusion group
OS is defined as the time from CIK-cell infusion to death from any cause.
Time frame: from enrollment to the end of treatment at 15 years
EFS in mRNA-CIK infusion group
EFS is defined as the time from mRNA-CIK-cell infusion to the earliest relapse, death from any cause, or treatment failure
Time frame: 2-year EFS rate
Plan to share: No
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Beijing GoBroad Hospital