Clinical trial · Interventional
Gene Therapy for B-Cell Non-Hodgkin Lymphoma Using CD19 CAR Gene Transduced T Lymphocytes
Clinical Research of Gene Therapy for Refractory B-Cell Non-Hodgkin Lymphoma Using Autologous T Cells Expressing a Chimeric Antigen Receptor Specific to the CD19 Antigen
- 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, efficacy and blood kinetics of autologous T cells genetically modified to express anti-CD19 Chimeric Antigen Receptor in patients with relapsed or refractory B-Cell Non-Hodgkin 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 |
|---|---|---|---|
| Relapsed or Refractory B-Cell Non-Hodgkin Lymphoma | — | UNRESOLVED | — |
Interventions
Interventions (4)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Cyclophosphamide or Bendamustine | Drug | — | UNRESOLVED |
| Dose Level -1 | Genetic | — | UNRESOLVED |
| Dose Level 2 | Genetic | — | UNRESOLVED |
| Dose Level 3 | Genetic | — | UNRESOLVED |
Design
Arms and outcomes
Arms (4)
- type
- EXPERIMENTAL
- label
- Dose Level -1
- description
- Cyclophosphamide or Bendamustine as Pre-treatment, and in combination with CD19-CAR-T. In case when sufficient cell number of CD19-CAR-T has been manufactured, the physician judges whether the 2nd infusion of CD19-CAR-T should be performed based on the condition of the subject.
- interventionNames
- Drug: Cyclophosphamide or Bendamustine
- Genetic: Dose Level -1
- type
- EXPERIMENTAL
- label
- Dose Level 1
- description
- Cyclophosphamide or Bendamustine as Pre-treatment, and in combination with CD19-CAR-T. In case when sufficient cell number of CD19-CAR-T has been manufactured, the physician judges whether the 2nd infusion of CD19-CAR-T should be performed based on the condition of the subject.
- interventionNames
- Drug: Cyclophosphamide or Bendamustine
- Genetic: Dose Level 1
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 20 Years
- Maximum age
- 70 Years
Show eligibility criteria text
Inclusion Criteria: 1. Relapsed or refractory B-NHL. 2. Evaluable region can be identified by CT scan and is positive by FDG-PET. 3. 20 ≤ age ≤ 70 years at the time of informed consent. 4. ECOG performance status of 0-2. 5. Well preserved main organ functions. 6. Life expectancy ≥3 months after informed consent. 7. Written informed consent. Exclusion Criteria: 1. Other active malignancy. 2. CNS infiltration of lymphoma. 3. History of allogeneic stem cell transplantation. 4. Already participated in a clinical trial in which CD19-CAR-T are administered within 24 weeks. 5. Concurrent use of systemic steroids or immunosuppressive agents. 6. Concurrent severe heart disease. 7. History of severe cerebrovascular disease or sequela including paralysis. 8. Known active or severe infection. 9. HIV seropositive status. 10. HBsAg-positive or both HBcAb and HBV-DNA positive. 11. Active hepatitis C. 12. Psychiatric disorder or drug addiction that affects the ability of informed consent. 13. Pregnant or breastfeeding women, women who may be pregnant and women desiring to become pregnant. Men who desire impregnating a woman are also excluded (excluded: in case when sperm is cryopreserved prior to gene therapy and a child is born by using the sperm). 14. Any other patients judged by the investigators to be inappropriate for the subject of this study.
References
Publications (0)
Data not yet available