It is a single-arm, open-label clinical study to assess the safety and efficacy of the C752 CAR-T Cells for patients with CD19+ refractory/relapsed B cell non-Hodgkin lymphoma.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
2
C752 will be administered on Day 0
920th Hospital of Joint LogisticsSupport Force of People's Liberation
Kunming, Yunnan, China
The incidence and severity of adverse events (AEs)
Time frame: 1 year
Dose Limiting Toxicities
Time frame: First 28 days s after C752 injection
Objective response rate (ORR)
Objective response rate after C752 injection as defined by Lugano 2014
Time frame: 1 year
PFS
Time frame: 1 year
Pharmacokinetic - AUC
Time frame: 1 year
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