About this trial
A phase I clinical study of the safety and tolerability, efficacy of CNCT19 CAR T-cell therapy in patients with advanced hepatocellular carcinoma hepatocellular carcinoma.
Eligibility criteria
Qualifiers
Aged 18 to 80 years, male or female;
Subjects voluntarily participated in the research and signed the Informed Consent Form (ICF) by themselves or their guardians;
Pathologically diagnosed with hepatocellular carcinoma, patients with China liver Cancer Staging (CNLC) stageII-III.;
HCC patients who are not suitable for surgical resection or local treatment (including ablation therapy, interventional therapy, and radiation therapy), or who experience recurrence or progression after surgery and/or local treatment, and who have previously received at least second-line systematic standardized treatment and have progressed or are intolerant to it;
Disqualifiers
Active brain metastasis;
Patients who have received or are waiting for organ transplantation;
Active autoimmune diseases that require systemic immunosuppressive therapy within the past 2 years, such as systemic lupus erythematosus, rheumatoid arthritis, ulcerative colitis, etc;
Researchers evaluated that the proportion of intrahepatic tumors is greater than 50% of the entire liver; Or there may be tumor thrombus formation in the main portal vein, or tumor thrombus invasion into the mesenteric vein/inferior vena cava;
Trial design
Treatments tested in this trial
- anti-CD19 CAR-T
Treatment groups
Sponsors and collaborators
Zhejiang University
Lead sponsor
Juventas Cell Therapy Ltd.
Collaborator