Clinical trial · Interventional
CD70-targeted CAR-NKT Cells(CGC729) Therapy in the Renal Cell Carcinoma
A Phase I Clinical Study to Assess the Safety and Efficacy of CD70-targeted CAR-NKT in the Treatment of Relapsed or Metastatic Advanced Renal Cell Carcinoma.
NCT06182735CI-TRIAL-00072593unknownPhase 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 phase I, open-label, single-arm study conducted to evaluate the safety, tolerability, PK, and preliminary efficacy of CGC729 with Relapsed or Metastatic advanced renal cell carcinoma. Condition or disease:Renal Cell Carcinoma Intervention/treatment: Biological: CD70 CAR-NKT cells Phase 1
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 |
|---|---|---|---|
| Renal Cell Carcinoma | Renal Cell Carcinoma | CURATED_BROADER | 0.80 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Cyclophosphamide + Fludarabine + Infusion of CAR-NKT Cells | Combination Product | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Cyclophosphamide + Fludarabine + Infusion of CAR-NKT Cells
- description
- Lymphodepleting regimen, Cyclophosphamide 250mg/m2 IV on day -5 to -3 and Fludarabine 25mg/m2 IV on days -5 to -3. Followed by infusion of CAR-NKT on day 0. Potential CGC729 doses: Dose level 1: 5.0×106 CAR- NKT cells/m2; Dose level 2: 1.5×107 CAR- NKT cells/m2; Dose level 3: 4.5×107 CAR- NKT cells/m2.
- interventionNames
- Combination Product: Cyclophosphamide + Fludarabine + Infusion of CAR-NKT Cells
Primary outcomes (1)
- measure
- Percentage of Participants Experiencing DLT
- timeFrame
- Day 28 after CGC729 infusion
- description
- 1.Percentage of Participants Experiencing Dose Limiting Toxicities (DLTs) Dose limiting toxicity (DLT) is an AE that meets the following criteria and occurs within 28 days of CGC729 infusion.AE is graded according to CTCAE version 5.0.
Secondary outcomes (6)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: 1. Subjects or their guardians agree to participate in this clinical trial and sign the ICF, indicating that they understand the purpose and procedures of this clinical trial and are willing to participate in the research. 2. Age 18 to 75 years. 3. Patients with advanced clear cell renal cell carcinoma confirmed by histology or cytology to be recurrent or metastatic after at least second-line treatment. 4. Archival and/or fresh tumor tissue samples are required. 5. At least one measurable lesion at baseline per RECIST version 1.1. 6. ECOG 0-1 points. 7. The expected survival time is more than 12 weeks. 8. The functions of important organs are basically normal: Hematopoietic function: neutrophils 1.5×109/L, platelets 75×109/L, hemoglobin 80g/L; Renal function: creatinine clearance of ≥60 mL/min.; Liver function: ALT and AST≤2.5×ULN (≤5 × ULN for patients with liver metastases); Total bilirubin≤1.5×ULN. Coagulation INR \< 1.7. 9. Pregnancy tests for women of childbearing age shall be negative, Both men and women agreed to use effective contraception. Exclusion Criteria: 1. Pregnant or lactating female subjects. 2. Pregnant or lactating female subjects. 3. Known positive test result for human immunodeficiency virus (HIV) oracquired immune deficiency syndrome (AIDS). 4. Active infection or uncontrollable infection. 5. Known to have active or uncontrolled autoimmune diseases, such as Crohns disease, rheumatoid arthritis, systemic lupus erythematosus, etc. . 6. Having a history of any mental illness, including dementia, altered mental status, which may affect informed consent and the understanding of the subject by the relevant questionnaire. 7. Have a serious uncontrollable illness that may affect the subject receiving treatment for this study. 8. Subjects with other malignant tumors within the past 2 years, except basal or squamous skin cancer, superficial bladder cancer, and breast cancer in situ, have been completely cured and do not need follow-up treatment. 9. Subjects who are using systemic steroids or steroid inhalers for treatment. 10. Use of anti-CD70 therapy or cell therapy within the previous 3 months. 11. Immunotherapy, targeted drug therapy or chemotherapy within 5 drug half-lives within 2 weeks before cell infusion. 12. Subjects allergic to immunotherapy or related drugs. 13. Patients with leptomeningeal metastasis or central nervous system metastasis, and definite central nervous system underlying diseases with significant symptoms in the past 6 months. 14. Subjects with NYHA heart failure class ≥2 or hypertension uncontrolled by standard therapy requiring special treatment, previous history of myocarditis, or myocardial infarction within 6 months. 15. Earnestly received or organ transplantation or preparing to receive organ transplants. 16. Other investigators deem it unsuitable to participate in the study.
References
Publications (0)
Data not yet available
No reference posted for this study.