Evaluate the Safety and Efficacy of JCXH-213 in Patients with Relapsed/Refractory B-cell non-Hodgkin Lymphoma
Patient will receive study treatment in the treatment observation period. After the end of the treatment observation period, patients will be allowed to continue to receive treatment if there is no major safety problems and the investigator judges that the patient may continue to benefit.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
8
JCXH-213 infusion
Department of Lymphoma and Myeloma, Yuhengnan Road, Changping District, Beijing
Beijing, China
RECRUITINGDose limiting toxicity (DLT).
Time frame: The DLT observation period is 21 days after first infusion of JCXH-213.
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