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RecruitingNCT06389305Updated Feb 25, 2026

CIK Cell Therapy for Relapsed or Refractory Acute B-Lymphoblastic Leukemia: Prognostic Impact on Patients With Early CAR-T Cell Dysfunction

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

From the registry’s dates

  • Primary completion was expected by May 2026, 4 months ago, but the record still lists the study as recruiting.
  • Started May 2024; still recruiting 2 years 4 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
213
Allocation
Randomized
Ages
1 Year to 39 Years
Sex
All
01

Study summary

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.

02

Conditions studied

  • B-cell Acute Lymphoblastic Leukemia
  • Acute Lymphoblastic Leukemia, in Relapse
  • Refractory Acute Lymphoid Leukemia
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In context

Burkitt Lymphoma

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 →

Lead sponsor

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.

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Who can participate

Ages eligible
1 Year to 39 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • A patient must meet all of the following to be enrolled:

    1. A confirmed diagnosis of refractory or relapsed B-ALL (criteria reference: NCCN, 2024.4), where all patients meet the National Comprehensive Cancer Network(NCCN) guidelines for the diagnosis of acute lymphoblastic leukemia (hematopathological examination of bone marrow aspirate and biopsy tissue showing ≥20% lymphoblasts in the bone marrow, confirmed by comprehensive flow cytometry (FCM) immunotyping, minimal residual disease analysis, and G-banded metaphase chromosome karyotype analysis). Molecular characteristics can be described through methods such as interphase fluorescence in situ hybridization (FISH) testing, reverse transcription polymerase chain reaction (RT-PCR) testing, and next-generation sequencing (NGS) for comprehensive detection of fusion genes and pathogenic mutations. Determination can also be made by the World Health Organization's subtypes of acute lymphoblastic leukemia, as well as cytogenetic and clinical risk groups.
    2. Loss of CAR-T cell activity within 6 months after previous CAR-T therapy and no relapse.
    3. Age between 1 and 39 years old.
    4. No severe allergic constitution.
    5. Eastern Cooperative Oncology Group (ECOG) performance status score of 0-2.
    6. Life expectancy, as judged by the investigator, of at least 60 days.
    7. Patients with self-awareness between 8 and 39 years of age voluntarily sign an informed consent, and the legal representative (guardians) of child patients under 18 years of age voluntarily signs an informed consent.

Exclusion criteria

Exclusion Criteria:

  • A patient with at least one of the following conditions will be excluded:

    1. Received bendamustine treatment within the past 9 months;
    2. Intracranial hypertension or impaired consciousness in the brain;
    3. Symptomatic heart failure or severe arrhythmia;
    4. Symptoms of severe respiratory failure;
    5. With other types of malignant tumors;
    6. Disseminated intravascular coagulation;
    7. Serum creatinine and/or blood urea nitrogen ≥ 1.5 times the normal value;
    8. Suffering from sepsis or other uncontrollable infections;
    9. Uncontrollable diabetes;
    10. Severe mental disorders;
    11. Significant lesions in the brain as detected by head magnetic resonance imaging;
    12. Leukemic cells in the cerebrospinal fluid >20 cells/μL;
    13. Peripheral blood leukemic cell proportion >30%;
    14. Have undergone organ transplantation;
    15. Female patients (those with childbearing potential) are pregnant or lactating;
    16. Active or uncontrollable infectious diseases, such as hepatitis (HBV, HCV), HIV, or syphilis.
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
213 participants (estimated)

Study arms

  • Placebo comparator
    peripheral blood lymphocytes

    Drug: peripheral blood lymphocytes

  • Experimental
    CIK cells

    Drug: CIK cell

Interventions

  • Drugperipheral blood lymphocytes

    autologous or allogeneic peripheral blood lymphocytes

  • DrugCIK cell

    autologous or allogeneic cytokine-induced killer (CIK) cells

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What researchers measure

Primary outcomes

  1. 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

Secondary outcomes

  1. 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

  2. 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

  3. 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

  4. 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

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Study locations

1 of 1 sites recruiting
  • Beijing GoBroad Hospital
    Beijing, Beijing Municipality 102206, China
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 25, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06389305
Lead sponsor
Beijing GoBroad Hospital
Responsible party
Jing Pan (Director of Dept of Hemato-Oncology and Immunotherapy, Beijing GoBroad Hospital) — Principal investigator
First posted
Apr 29, 2024
Start date
May 27, 2024
Primary completion
May 30, 2026 (estimated)
Completion
May 30, 2026 (estimated)
Last update
Feb 25, 2026

Study contacts

Tengyu Wang
Contact
tengyu.wang@gohealtharo.com
86+18333186020

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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