Clinical trial · Interventional
CAR - γ δ T Cells in the Treatment of Relapsed and Refractory CD7 Positive T Cell-derived Malignant Tumors
Clinical Application of Chimeric Antigen Receptor Modified γδ T Cells(CAR - γ δ T Cells) in Relapsed and Refractory CD7 Positive T Cell-derived Malignant Tumors
- 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 study on the clinical application of chimeric antigen receptor modified γδ T cells (CAR - γδ T cells) in relapsed and refractory CD7 Positive T cell-derived malignant tumors.The main purpose of this study was to evaluate the efficacy of car - γ δ T cell infusion in patients with relapsed and refractory CD7 Positive T cell-derived malignancies.
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 |
|---|---|---|---|
| CAR | — | UNRESOLVED | — |
| Malignant Tumors | Malignant Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Chimeric antigen receptor modified γδ T cells | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- CAR-γδT
- description
- Infusion,iv,0.2-5 ×10\^6/ kg,once.
- interventionNames
- Drug: Chimeric antigen receptor modified γδ T cells
Primary outcomes (1)
- measure
- ORR 3
- timeFrame
- three months after CAR-T cells infusion
- description
- 3-month objective response rate
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 14 Years
- Maximum age
- 70 Years
Show eligibility criteria text
Inclusion Criteria: 1. the patients must be patients with relapsed or refractory CD7 Positive T cell-derived malignancies, who have at least one course of standard regimen chemotherapy and one course of salvage regimen chemotherapy and have poor effect; 2. Researchers believe that there is no other feasible and effective alternative treatment, such as hematopoietic stem cell transplantation; 3. Patients should have indicators for detection or evaluation of disease, including detection of minimal residual disease (MRD) by immunophenotyping, cytogenetics or PCR; 4. They are 14-70 years old, regardless of gender or race; 5. Physical condition: ECoG score 0-2; 6. Cardiac function: left ventricular ejection fraction greater than or equal to 40%; 7. The expected survival time was \> 12 weeks; 8. Serum creatinine (CR) ≤ 1.5 × ULN (upper limit of normal value), alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 2.5 × ULN, total bilirubin ≤ 1.5 × ULN; 9. Patients have self-knowledge ability and can sign informed consent; 10. The guardian of the child patient agreed to sign the informed consent. Exclusion Criteria: 1. pregnant or lactating women; 2. Uncontrolled infection; 3. Active HBV or HCV infection; 4. People living with HIV; 5. Less than 100 days after allogeneic hematopoietic stem cell transplantation; 6. Patients with acute GVHD or chronic GVHD after allogeneic hematopoietic transplantation; 7. Patients receiving GVHD treatment.
References
Publications (0)
Data not yet available