This study is to provide locally produced, bispecific CD19 CD20 CAR T cells to patients with B-cell lymphoma/leukemia who have no access to commercial CAR T cells or who have relapsed thereafter. The primary objective is to assess the safety of bispecific anti-CD19, anti- CD20 CAR T cell-therapies after lymphodepleting chemotherapy in patients with B cell malignancies with exhausted standard treatment options.
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Evaluation of Adverse Events
Timeframe: up to 3 months after CAR T cell infusion
Evaluation of Adverse Events of special interest (CRS)
Timeframe: up to 3 months after CAR T cell infusion
Evaluation of Adverse Events of special interest (ICANS)
Timeframe: up to 3 months after CAR T cell infusion
Evaluation of Adverse Events of special interest (ICAHT)
Timeframe: up to 3 months after CAR T cell infusion