OncoMatch/Clinical Trials/NCT06828341
A Single-arm, Open, Exploratory Clinical Study of Allogeneic CAR-T Cells in the Treatment of Relapsed/Refractory Brain Gliomas With Positive CD70 Expression
Is NCT06828341 recruiting? Yes, currently enrolling (May 2026). This Early Phase 1 trial studies CAR-T for gliomas.
Treatment: CAR-T — The goal of this clinical trial is to learn if allogeneic CAR-T cells can treat patients with advanced gliomas. The main questions it aims to answer are: Evaluate the safety of allogeneic CAR-T cells in the treatment of advanced gliomas. To evaluate the effectiveness of allogeneic CAR-T cells in the treatment of advanced gliomas and to study its immunological properties in patients.
Check if I qualifyExtracted eligibility criteria
Biomarker criteria
Required: CD70 overexpression (IHC ≥2+)
CD70 expression in the tumor site of the subject meets the positive standard, that is, ≥2+
Prior therapy
Must have received: standard treatment
have failed or cannot tolerate standard treatment
Cannot have received: CD70-targeted therapy
Patients who have received any treatment related to the CD70 target within 3 years
Cannot have received: experimental drug or device
Patients who have received any experimental drug treatment or used experimental devices within 28 days before CAR-T administration
Cannot have received: systemic anti-tumor treatment
Patients who have received any systemic anti-tumor treatment within 28 days or 5 half-lives (whichever is longer) before CAR-T administration, including systemic chemotherapy, immunotherapy, hormone therapy (excluding glucocorticoids), targeted therapy, systemic immunomodulators (including but not limited to interferon, interleukin 2 and tumor necrosis factor), and received Chinese herbal medicine or Chinese patent medicine with anti-tumor effects within 14 days before CAR-T administration
Cannot have received: radiotherapy
Patients who have received radiotherapy within three months before administration
Cannot have received: non-CD70 target cell therapy products
Patients who have received other non-CD70 target cell therapy products within two months before administration
Cannot have received: other cell therapy products
Patients who have received other cell therapy products in the past need to undergo RCL testing during the screening period, and patients with positive results in any test
Cannot have received: therapeutic glucocorticoids
Exception: physiological replacement doses allowed (e.g., prednisone ≤10 mg/day or equivalent)
Patients who have received therapeutic doses of glucocorticoids within 14 days before CAR-T administration (however, physiological replacement doses of glucocorticoids are allowed, such as 10 mg/day prednisone or equivalent)
Lab requirements
Blood counts
ANC ≥ 1.5×10^9/L; platelets ≥ 90×10^9/L (no transfusion/auxiliary support within 14 days); WBC ≥ 3.0×10^9/L; HGB ≥ 9.0 g/dL
Kidney function
serum creatinine ≤ 1.5x ULN or creatinine clearance ≥ 50 mL/min
Liver function
serum bilirubin (T-Bil) ≤ 1.5x ULN; AST/ALT ≤ 3x ULN (≤5x ULN with liver metastasis); Gilbert's syndrome exception
Cardiac function
QTc interval ≤ 450 ms (men), ≤ 470 ms (women); LVEF ≥ 50%; no severe cardiovascular disease
Subjects have adequate organ and bone marrow function and meet the following laboratory test standards: ... see full criteria for details
Structured fields extracted by AI. May contain errors — verify against the official protocol.
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