Clinical trial · Interventional
CD19 Targeted CAR T Cell Therapy in Patients With Relapsed/ Refractory B Cell Acute Lymphoblastic Leukaemia (ALL)
Phase I Clinical Trial Evaluating Safety of CD19 CAR-T Cells in Patients With Relapsed or Refractory Acute B-cell Lymphoblastic Leukemia (R/R B-ALL)
NCT04653493CI-TRIAL-00050795unknownPhase 1ClinicalTrials.gov clinicaltrialsProvenance
- 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 is a single-arm, open-label, phase I study (safety and dose escalation) of autologous Chimeric Antigen Receptor (CAR) T-cells targeting CD19 in patients with relapsed/refractory B cell acute lymphoblastic leukemia (ALL).
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Refractory B Cell Acute Lymphoblastic Leukemia (ALL) | B Acute Lymphoblastic Leukemia | CURATED_BROADER | 0.78 |
| Relapsed B Cell Acute Lymphoblastic Leukemia (ALL) | B Acute Lymphoblastic Leukemia | CURATED_BROADER | 0.78 |
Interventions
Interventions (4)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| CD19 CAR engineered autologous T-cells | Biological | — | UNRESOLVED |
| Cyclophosphamide | Drug | Cyclophosphamide | ALIAS |
| Fludarabine | Drug | Fludarabine | ALIAS |
| Mesna | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- CD19 CAR-T cells
- description
- Pediatric or adolescent/young adult patients with CD19+ relapsed or refractory B cell acute lymphoblastic leukemia (R/R B-ALL)
- interventionNames
- Biological: CD19 CAR engineered autologous T-cells
- Drug: Cyclophosphamide
- Drug: Fludarabine
- Drug: Mesna
Primary outcomes (1)
- measure
- Maximum Tolerated Dose (MTD) and Dose-limiting Toxicities (DLT) of CD19 CAR-T cells
- timeFrame
- Within 30 days after the last dose of CD19 CAR-T cells
- description
- Patients will be continually assessed for unexpected adverse events using the NCI CTCAE (version 5.0) or unexpected early mortality 30 days post-infusion. The primary objectives for the Phase I study portion are to determine the maximum tolerated dose (MTD) and characterize the safety profile and dose-limiting toxicities (DLTs) of treatment with CD19 CAR-T cells in pediatric, adolescent and young adult patient's ≤ 25 years of age, with relapsed/refractory CD19+ ALL.
Eligibility
Eligibility (as posted)
- Sex
- All
- Maximum age
- 25 Years
Show eligibility criteria text
Inclusion Criteria: CD19+ ALL patients with any of the following: 1. Relapsed or Refractory CD19 positive B-cell acute lymphoblastic leukemia (R/R B-ALL) A. Primary refractory disease despite at least 2 cycles of an intensive chemotherapy regimen designed to induce remission B. Refractory disease despite salvage therapy C. 2nd or greater relapse D. Any relapse after allogeneic hematopoietic stem cell transplantation 2. Informed consent explained to and signed by patient/parents or legal guardian. 3. The Karnofsky (age ≥10 years)/Lansky (age \<10 years) performance status score over 50 points. 4. Expected to survive for more than 3 months. 5. Patients with a history of prior allogeneic hematopoietic stem cell transplant (HSCT) must be at least 3 months from HSCT at the time of CD19 CAR-T cells infusion and also have not received a donor lymphocyte infusion (DLI) within the 28 days prior to apheresis. 6. Important organ function is satisfied: Heart ultrasound indicates cardiac ejection fraction ≥ 50%, no obvious abnormality in ECG; Adequate pulmonary function defined as forced vital capacity (FVC) ≥ 50% of predicted value; or pulse oximetry ≥ 92% on room air if the patient is unable to perform pulmonary function testing; creatinine clearance calculated by Cockcroft-Gault formula ≥ 50 ml/min/1.73m2; Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) ≤ 5 times the upper limit of normal for age; Total Bilirubin ≤ 3 times the upper limit of normal for age. 7. Absolute lymphocyte count ≥ 0.5 x 10⁹/L. 8. Hemoglobin ≥ 8 g/dl (can be transfused). 9. Platelet count ≥ 20,000/μL (can be transfused). 10. Meets eligibility criteria to undergo autologous apheresis. Exclusion Criteria: 1. Isolated extra-medullary disease relapse. 2. Active CNS involvement of ALL (CNS Grade 3 per National Comprehensive Cancer Network guidelines). 3. Severe, uncontrolled bacterial, fungal or viral infections (Active hepatitis B or C, history of HIV infection) 4. Pre-existing significant neurological disorder. 5. Active significant acute graft versus host disease (GVHD) or moderate/severe chronic GVHD requiring systemic steroids or other immunosuppressants within 4 weeks of enrolment. 6. Pregnant or lactating female. 7. The patient did not agree to use effective contraception during the treatment period and for the following 1 year. 8. A history of other malignant tumors. 9. Receiving systemic steroids therapy exceeding the equivalent of 0.5 mg/ kg/day of methylprednisolone, in the 7 days prior to CAR T-cell infusion 10. Receiving systemic immunosuppressive therapy in the 14 days prior to CAR T-cell infusion 11. Receiving intrathecal chemotherapy in the 7 days prior to CAR T-cell infusion
References
Publications (0)
Data not yet available
No reference posted for this study.