This is a single-center, open-label, exploratory clinical study to evaluate the efficacy and safety of IASO207 Injection in patients with Relapsed/Refractory B-cell Malignancies。
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Safety endpoint - Adverse Events (AEs)
Timeframe: up to 2 years from IASO207 Injection infusion
Safety endpoint - The incidence of dose-limiting toxicity (DLT)
Timeframe: up to 28 days from IASO207 Injection infusion
Safety endpoint - The types,incidence and severity of abnormal laboratory tests
Timeframe: up to 2 years from IASO207 Injection infusion