Clinical trial · Interventional
Anti-CD19 CAR-Engineered NK Cells in the Treatment of Relapsed/Refractory Acute Lymphoblastic Leukemia
A Phase Ⅰ Clinical Study on the Safety and Efficacy of Chimeric Antigen Receptor Gene Modified NK Cells Targeting CD19 in Patients With Recurrent or Refractory CD19 Positive Acute Lymphoblastic Leukemia
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This study is a single arm clinical study to observe the safety ,dose tolerance and pharmacokinetic characteristics of CAR NK-CD19 in patients with recurrent or refractory CD19 positive acute lymphoblastic leukemia, and preliminarily evaluate the effectiveness, the immunogenicity of the product and the correlation between the changes of cytokines after infusion and CRS , ICANS.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Acute Lymphoblastic Leukemia | Acute Lymphoblastic Leukemia | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| CAR-NK-CD19 Cells | Biological | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- CAR-NK-CD19 Cells
- description
- After preconditioning with chemotherapy, CAR-NK-CD19 Cells will be evaluated.
- interventionNames
- Biological: CAR-NK-CD19 Cells
Primary outcomes (6)
- measure
- Safety of CAR NK-CD19 Cell
- timeFrame
- Up to 3 months after cell infusion
- description
- Incidence of adverse events associated with CAR NK-CD19 treatment, abnormal clinically significant laboratory findings, including dose-limiting toxicity (DLT) and maximum-tolerated Dose (MTD).
- measure
- Cell count of CAR NK-CD19
- timeFrame
- From 1 to 720 days after infusion
- description
- CAR NK-CD19 cell count
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 3 Years
Show eligibility criteria text
Inclusion Criteria: * Age ≥12 years in the single-dose exploration phase, age ≥3 years in the dose exploration phase, both sexes; * Meet the diagnostic criteria for recurrent or refractory CD19 positive acute lymphoblastic leukemia. * The main organs have good organ function. * The estimated survival time is ≥12 weeks. * Blood pregnancy tests for women of childbearing age are negative. * The patient himself/herself , and/or his/her legal guardian, agree to participate in the trial and sign the informed consent form. Exclusion Criteria: * Central nervous system involvement; * Simple extramedullary leukemia or simple extramedullary recurrence; * Received hematopoietic stem cell transplantation within the last 3 months and had graft-versus-host disease (GVHD) in the last 2 weeks, requiring immunosuppressive agents; * Treated with high-dose corticosteroids in the last 1 week; * Allogeneic cell therapy, major surgery, and live or attenuated vaccine had been received within 4 weeks prior to CAR NK-CD19 infusion; * Had received other antitumor therapy or had an uncontrolled infection within 2 weeks prior to CAR NK-CD19 infusion; * Systemic steroids were used within 3 days before CAR NK-CD19 infusion; * Toxicity caused by previous treatment do not fully recover or do not stabilize to grade 1; * Concomitant autoimmune diseases, central nervous system diseases, other active malignancies, infectious diseases, severe cardiovascular diseases, etc; * Known allergies to study drugs or drugs that may be used in the study; * Other conditions determined by Investigator which are not suitable for participation in the study
References
Publications (0)
Data not yet available