The purpose of this study is to evaluate the safety and effectiveness of CAR-pNK cell immunotherapy in patients with CD7 positive relapsed or refractory Leukemia and Lymphoma.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
10
The allogeneic NK cells (NK-92 cell line for clinical use) are engineered to contain anti-CD7 attached to TCRzeta, CD28 and 4-1BB signaling domains. These modified cells are called chimeric antigen receptor NK cells with specificity for CD7.
PersonGen BioTherapeutics (Suzhou) Co., Ltd.
Suzhou, Jiangsu, China
RECRUITINGAdverse events attributed to the administration of the anti-CD7 CAR-pNK cells
Determine the toxicity profile of the CD7 targeted CAR-pNK cells with Common Toxicity Criteria for Adverse Effects (CTCAE) version 4.0.
Time frame: 2 years
Clinical response to CD7 CAR-pNK cell infusions
Patients with measurable disease will be assessed for the response of their disease to CD7 CAR-pNK cell treatment.
Time frame: Safety follow-up is 100 days from last CAR-pNK infusion
Determine the existence of CD7-CAR-pNK in vivo
Time frame: 1 year
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