Clinical trial · Interventional
CD19/CD20 Dual-CAR-T in B-cell Lymphoma Patients
CD19/CD20 Dual-CAR-T for Patients With B-cell Lymphoma
NCT04260932CI-TRIAL-00056966completedPhase 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 center, single arm, open-label, phase I study to evaluate the safety and efficacy of CD19/CD20 Dual-CAR-T cells in patients with refractory and relapsed B-cell lymphoma.
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 |
|---|---|---|---|
| B-cell Lymphoma | B-Cell Malignant Neoplasm | CURATED_BROADER | 0.80 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| CD19/CD20 Dual-CAR-T cells | Biological | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- CD19/CD20 Dual-CAR-T cells
- description
- CD19/CD20 Dual-CAR-T cells are prepared via lentiviral infection. 5 days prior to infusion of CAR-T cells, subjects receive fludarabine at dose 30mg/m2/day and cyclophosphamide treatment at dose 250mg/m2 for 3 days and take a rest for at least 2 days before infusion.
- interventionNames
- Biological: CD19/CD20 Dual-CAR-T cells
Primary outcomes (2)
- measure
- Percentage of participants with adverse events.
- timeFrame
- 6 months
- measure
- Objective remission rate(ORR)
- timeFrame
- 6 months
- description
- The percentage of participants who achieved complete remission (CR) and partial remission over all participants.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 1 Year
- Maximum age
- 80 Years
Show eligibility criteria text
Inclusion Criteria: 1. Relapsed and refractory B-cell lymphoma with: Relapsed or refractory disease after ≥2 lines of chemotherapy including rituximab and anthracycline and either having failed after autologous or allogeneic hematopoietic stem cell transplantation (ASCT); 2. Patients must have evaluable evidence of disease, including minimal residual disease (MRD); 3. Double positive expression of CD19 / CD20 in B cells; 4. Ages 1 to 80 years, including boundary values; 5. ECOG score 0-3 points; 6. Women of childbearing age (15-49 years old) must receive a pregnancy test within 7 days prior to initiation of treatment and the results are negative; male and female patients with fertility must use an effective contraceptive to ensure 3 months after discontinuation of treatment during the study period not pregnant inside; 7. Patients who voluntarily sign informed consent and are willing to comply with treatment plans. Exclusion Criteria: 1. patients with organ failure: * Heart: NYHA heart function grade IV; * Liver: Grade C that achieves Child-Turcotte liver function grading; * Kidney: kidney failure and uremia; * Lung: symptoms of respiratory failure; * Brain: a person with a disability; 2. Active infections that are difficult to control; 3. Human immunodeficiency virus (HIV) positive; 4. Liver and kidney function: total bilirubin \> 5 × ULN, aspartate aminotransferase (AST) and alanine aminotransferase (ALT) \> 5 × ULN, serum creatinine clearance rate 60mL / min; 5. GVHD ≥ 2 or anti-GVHD treatment; 6. intracranial hypertension or unconsciousness; respiratory failure; diffuse vascular internal coagulation; 7. pregnant or lactating women; 8. The patient does not agree to use effective contraception during the treatment period and for the next 3 months; 9. Patients who participate in other clinical studies at the same time; 10. The investigator believes that there are other factors that are not suitable for inclusion or influence the subject's participation or completion of the study.
References
Publications (0)
Data not yet available
No reference posted for this study.