Clinical trial · Interventional
Study of TBI-1501 for Relapsed or Refractory Acute Lymphoblastic Leukemia
A Multicenter Phase I/II Study for Relapsed or Refractory CD19+ B-acute Lymphoblastic Leukemia
NCT03155191CI-TRIAL-00082742TBI-1501active not recruitingPhase 1 / Phase 2ClinicalTrials.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)
Evaluate the safety (P-I), pharmacokinetics and anti-tumor effect of immunotherapy of autologous T cells genetically modified to express anti-CD19 chimeric antigen receptor (CAR) (TBI-1501) for relapsed or refractory CD19+ B-cell acute lymphoblastic leukemia.
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 |
|---|---|---|---|
| Lymphoblastic Leukemia, Acute Adult | Acute Lymphoblastic Leukemia | ONTOLOGY_EXACT | 0.85 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| TBI-1501 | Biological | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Dose Level -1 to 2
- description
- 0.3 to 3 x 10\^6 autologous CD19-CAR-T cells/kg per patient will be administered intravenously after a conditioning chemotherapy with cyclophosphamide. cohort -1: 3×10\^5 cells/kg cohort 1: 1×10\^6 cells/kg cohort 2: 3×10\^6 cells/kg.
- interventionNames
- Biological: TBI-1501
Primary outcomes (2)
- measure
- Phase-I portion: Number of participants with treatment-related adverse events as assessed by CTCAE v4.0
- timeFrame
- One year
- description
- Adverse event (frequency, seriousness, duration, causality, severity, classification), mortality, severe adverse event, discontinuation due to adverse event.
- measure
- Phase-II portion: Anti-tumor effect (CR+CRi rate)
- timeFrame
- 56 days
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 16 Years
Show eligibility criteria text
Inclusion Criteria: 1. In phase-1 study, patients must be ≥ 18 years of age. In phase-2 study, patients must be ≥ 16 years of age. 2. Patients with relapse or refractory CD19+ acute B-cell lymphoblastic leukemia 3. Patients must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1 or 2. 4. Patients must have adequate key organ function (bone marrow, heart, lung, liver, renal, etc), as defined below * Total bilirubin level ≤1.5xULN (Upper limit of normal) * AST(GOT)/ALT(GPT) level ≤5.0xULN * Serum creatinine ≤2.0mg/dL * SpO2 ≧ 92% * LVEF ≥50% 5. Patients must be able to understand and willing to sign a written informed consent document (for patients \<20 years of age their legal guardian must give informed consent). Exclusion Criteria: 1. White blood cell counts ≧ 50,000/uL 2. Received expected antitumor therapy (chemotherapy or radiation therapy, etc) within 2 weeks. 3. Received HSCT within 12 weeks before enrollment. 4. Under treatment for GVHD. 5. lymphocytes except for blasts ≦ 500/uL 6. Presence of active CNS-3 7. Concurrent use of systemic steroids or immunosuppressive agents (except for replacement therapy and local administration. e.g. inhalation, application and so on). 8. HBs Ag positive ,or either HBc Ab positive or HBs positive with HBV-DNA \> 1.3LogIU/ml 9. Presence of active hepatitis C infection 10. HIV Ab or anti-HTLV-1 Ab positive 11. History of allergy about component of investigational product or animal(cattle and/or mouse)-derived additives 12. Hypersensitivity to antibiotics. 13. Presence of symptomatic cardiac arrhythmias or serious heart disease. 14. Presence of another malignant tumor. 15. Psychiatric disorder, alcohol addiction or drug addiction that affects the ability of informed consent. 16. Active or serious infection. 17. Both men and women who have generative functions, and who cannot agree with using contraceptive devices from the day of the consent to the end of study. 18. Pregnant or lactating women. 19. Any other patients judged by the investigators to be inappropriate for the study.
References
Publications (0)
Data not yet available
No reference posted for this study.