This is a Phase I/II, Single-Arm, Open-Label, Multicentre Study to Evaluate the Safety and Efficacy of IMM0306 in Patients with Relapsed or Refractory B-Cell Non- Hodgkin's Lymphoma (R/R B-NHL).
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
154
IMM0306 is an bi-specific antibody
Cancer Hospital Chinese Academy of Medical Sciences
Beijing, China
RECRUITINGDose-limiting toxicity
Time frame: Evaluated for DLTs during the first 28-day cycle
Complete response rate
Time frame: up to 52 weeks
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