The purpose of this study is to evaluate the safety and efficacy of CD19-UCART in patients with r/r B-cell hematological malignancies.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
18
A conditioning therapy with cyclophosphamide and fludarabine will be conducted before ET-02 injection.
•The First Affiliated Hospital of Henan University of Science and Technology
Luoyang, Henan, China
Incidence of adverse events
Adverse events assessed according to NCI-CTCAE v5.0 criteria
Time frame: up to 2 years after lymphodepleting chemotherapy
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