This is a single-centre, single-arm and open-label study to investigate the safety and efficacy of anti CD19/CD22 CAR NK cells in patients with relapsed refractory B cell lymphoma.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
10
Total dose of 50-600 thousand /kg Anti-CD19/CD22 CAR NK cells will be administered at day0
Occurrence of treatment related adverse events as assessed by CTCAE v4.0
Defined as \>= Grade 3 signs/symptoms, laboratory toxicities, and clinical events) that are possibly, likely, or definitely related to study treatment.
Time frame: 1 year
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