Stopped: Because the implementation of the new regulation policy by the Chinese authority
This study is a single-arm, single-center, investigator-initiated clinical trial. The primary objective is to evaluate the safety and preliminary efficacy of administering universal CD19 CAR-T cells to subjects with refractory and relapsed B-cell tumors. Eligible participants will undergo FC lymphodepleting chemotherapy preconditioning after signing an informed consent form, followed by a one-time injection of universal UWD-19 to assess its safety and efficacy. Subjects will be hospitalized for a period, and after discharge, they will undergo periodic efficacy assessments and long-term survival follow-up for at least five years.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Maximum Tolerated Dose (MTD)
Timeframe: [Time Frame: Within the first month post-infusion.]
Dose-Limiting Toxicities (DLT)
Timeframe: [Time Frame: Within the first month post-infusion.]
Treatment-Emergent Adverse Events (TEAE)
Timeframe: [Time Frame: From the administration of UWD-19 CAR-T cells through six months post-infusion]