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Clinical Trials in China / NCT06515626
Recruiting Phase EARLY_PHASE1

Genetically Modified T Cells Treating Malignant Tumors

NCT06515626 · tracked via the Priya Life Science China tracker
Sponsor
Yi Zhang
Phase
Phase EARLY_PHASE1
Started
2024-08-18
Last updated
2024-09-25

Condition(s) studied

Solid Tumor

Investigational drug(s) / intervention(s)

CAR-T cell reinfusion

CAR-T cell reinfusion: Subjects were identified according to their benefit from the first treatment and target expression Whether to accept multiple returns; CAR-T cell reinfusion dose was 1\~10×106 cells/kg, and the reinfusion dose could be adjusted according to the tolerance of the subjects Usually intravenous infusion, but also according to the need for local interventional treatment or injection treatment

Study summary

To observe the safety, tolerability and initial effectiveness of gene modified T cell therapy in patients with malignant tumors in First Affiliated Hospital of Zhengzhou University, China.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: 1. Subjects with malignant tumors confirmed by histopathology or cytology, including: non-small cell lung cancer, esophageal squamous cell carcinoma, gastric cancer, colorectal cancer, liver cancer, pancreatic cancer, kidney cancer, cervical squamous cell carcinoma, ovarian cancer, breast cancer, melanoma, and brain glia tumor, lymphoma, etc.; 2. Age: 18 \~ 75 years old; Gender: no limitation; 3. Have sufficient hematopoietic capacity: ANC \>1500 cells /mm3, Blood plate count \>50,000 cells /mm3, HGB \>9.0g/dL, ALC \>9 cells /mm3; 4. Adequate liver and kidney function: AST and ALT ≤2.5 ULN in patients without liver metastasis and ≤5 times in patients with liver metastasis. ULN; Bilirubin ≤1.5 ULN (excluding hyperbilirubinemia or hyperbilirubin of non-hepatic origin); Creatinine ≤2.0 ULN. Creatinine clearance and creatinine clearance hormone ≥40 mL/min; 5. PT/INR \<1.5 ULN, and PTT/αPTT \<1.5 ULN; 6. For desirable tumor tissues or tissue white tablets, positive expression of at least one of Mesothelin, NKG2D, HER2, CD276, CD19, BCMA and other antigens can be selected for clinical trials; 7. ECOG physical status score 0 \~ 2 points; 8. Expected survival \>6 months; 9. Subject accepts voluntarily Exclusion Criteria: 1. Received anti-PD1, anti-PD-L1 or anti-PD-L2 antibody therapy or other immunotherapy methods one month before treatment with immune cells in this study; 2. History of organ transplantation; 3. Pregnancy or lactation; 4. Positive for high baseline HBV DNA levels (≥2000 IU/ml), HIV antibodies (anti-HIV), hepatitis C virus antibodies (anti-HCV), or treponema pallidum antibodies; 5. There is active infection; 6. There are active brain metastases (except asymptomatic or stable brain metastases after treatment); 7. Combined with a second tumor; With the exception of patients with basal cell carcinoma of the skin, superficial bladder cancer, squamous cell carcinoma of the skin, cervical carcinoma in situ, or papillary thyroid cancer who achieved complete response to the second tumor for more than 5 years and did not require treatment during the study period; 8. Severe autoimmune diseases such as ulcerative colitis, Crohn's disease, rheumatoid arthritis, systemic lupus erythematosus, autoimmune vasculitis, or Wegener's granulomatosis require long-term (more than 2 months) systemic immunosuppressive therapy; 9. People with allergies; 10. NYHA heart failure grade ≥2 or hypertension can not be controlled after standard treatment, have a history of myocarditis or have a heart attack within one year; 11. Thrombotic diseases with active bleeding that require treatment; 12. Patients who are determined by the researcher to have a serious uncontrollable disease or other conditions that may affect the treatment in this study and are considered unsuitable.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Zhengzhou University First Affiliated Hospital Zhengzhou Henan Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06515626 on ClinicalTrials.gov ↗ ← All trials in China