Clinical trial · Interventional
CD19 T-CAR for Treatment of Children and Young Adults With r/r B-ALL
A Single-Arm Phase I/II Study Evaluating the Safety and Clinical Efficacy Of the 2-nd Generation CD19 Autologous CAR T Cells on the CliniMACS Prodigy Automated Manufacturing Platform in Treatment of Paediatric And Young Adult Patients With Relapsed/Refractory B-lineage 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)
The purpose of this study is to evaluate the safety and efficiency of autologous CD19 CAR-T lymphocytes in a cohort of pediatric and young adult patients with relapsed /refractory B-lineage acute lymphoblastic leukemia
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 |
|---|---|---|---|
| Acute Lymphocytic Leukemia, Pediatric | Childhood Acute Lymphoblastic Leukemia | ALIAS | 0.90 |
| B-cell Acute Lymphoblastic Leukemia | B Acute Lymphoblastic Leukemia | ALIAS | 0.90 |
Interventions
Interventions (7)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Chimeric Antigen Receptor T-Cell Therapy | Biological | — | UNRESOLVED |
| Cyclophosphamide | Drug | Cyclophosphamide | ALIAS |
| Cytarabine | Drug | Cytarabine | ALIAS |
| Dexamethasone | Drug | Dexamethasone | ALIAS |
| Etoposide | Drug | Etoposide | ALIAS |
| Fludarabine | Drug | Fludarabine | ALIAS |
| Tocilizumab | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- experimental
- description
- Patients will receive lymphodepleting chemotherapy, one hour prior to infusion of CAR T-cells patients will receive tocilizumab IV 8 mg/kg (max 800 mg) over 1 hour. Patients then receive CD19-CAR T cells IV on day 0.
- interventionNames
- Biological: Chimeric Antigen Receptor T-Cell Therapy
- Drug: Fludarabine
- Drug: Cyclophosphamide
- Drug: Tocilizumab
- Drug: Cytarabine
- Drug: Etoposide
- Drug: Dexamethasone
Primary outcomes (5)
- measure
- Incidence of grade 3-5 SAE occurring within 30 days of CD19CAR T-cell infusion
- timeFrame
- 1 month
- description
- incidence of grade 3-5 SAE according to the Common Terminology Criteria for Adverse Events (CTCAE) version 4.03 occurring within 30 days of CD19CAR T-cell infusion
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 3 Months
- Maximum age
- 25 Years
Show eligibility criteria text
Inclusion Criteria: * Ability to give informed consent (for patients \> 14 years old). For subjects \< 18 years old their legal guardian must give informed consent * Patients with relapsed or refractory CD19-expressing B cell ALL : * Induction failure, no CR after course 2 or MRD\>0,1% after 3 courses of high-risk protocol * early bone marrow or combined relapse of acute lymphoblastic leukaemia, no CR or MRD\>0,1% after 1 course 2-nd line therapy * ALL post ≥ 2nd relapse, no CR or MRD\>0,1% after 1 course 2-nd line therapy * Relapse or MRD \>0,1% of ALL after stem cell transplant (\> 60 days post alloHSCT) * Late bone marrow or combined relapse of acute lymphoblastic leukaemia, no CR or MRD\>0,1% after 2nd course of 2-nd line therapy * There must be no available alternative curative therapies * CD19 expression must be detected on greater than 30% by flow cytometry * Patients must have measurable or evaluable disease at the time of enrolment, which may include any evidence of disease including minimal residual disease detected by flow cytometry, cytogenetics, or polymerase chain reaction (PCR) analysis. * Patient Clinical Performance Status: Karnofsky \>50% or Lansky \>50% * Patient Life Expectancy \> 8 weeks * Patients recovered from acute toxic effects of all prior chemotherapy, immuno- or radiotherapy * Patient absolute lymphocyte N \> or =100/mm3 * Patient cardiac function: left ventricular ejection fraction greater than or equal to 40% by MUGA or cardiac MRI, or fractional shortening greater than or equal to 28% by ECHO or left ventricular ejection fraction greater than or equal to 50% by ECHO. * Patients who agree to long-term follow up for up to 5 years (if received CD19 CAR-T cell infusion) Exclusion Criteria: 1. \<30% expression of CD19 on the leukemic population 2. Active hepatitis B, C or HIV infection 3. Oxygen saturation \< or = 90% 4. Bilirubin \>3x upper norma limit 5. Creatinine \>3x upper norma limit 6. Active acute GVHD overall grade ≥2 (Seattle criteria) 7. Moderate/severe chronic GVHD (NIH consensus) requiring systemic steroids 8. Clinical signs of grade \>3 CNS disorders (seizure disorder, paresis, aphasia, cerebrovascular, ischemia/hemorrhage, severe brain injuries, dementia, cerebellar disease, organic brain syndrome, psychosis, coordination or movement disorder) 9. Pregnant or lactating women. 10. Active severe infection
References
Publications (1)
- DERIVEDMaschan M, Caimi PF, Reese-Koc J, Sanchez GP, Sharma AA, Molostova O, Shelikhova L, Pershin D, Stepanov A, Muzalevskii Y, Suzart VG, Otegbeye F, Wald D, Xiong Y, Wu D, Knight A, Oparaocha I, Ferencz B, Roy A, Worden A, Kruger W, Kadan M, Schneider D, Orentas R, Sekaly RP, de Lima M, Dropulic B. Multiple site place-of-care manufactured anti-CD19 CAR-T cells induce high remission rates in B-cell malignancy patients. Nat Commun. 2021 Dec 10;12(1):7200. doi: 10.1038/s41467-021-27312-6. PMID 34893603