The study is evaluating the efficacy, and safety of SHR1459 combined with YY-20394 for Recurrent and refractory B-cell non-Hodgkin's lymphoma in adults.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
102
SHR1459 plus YY-20394
SHR1459 plus YY-20394
Gemcitabine-Oxaliplatin
Ruijin Hospital Affiliated to The Shanghai Jiao Tong University Medical School
Shanghai, Shanghai Municipality, China
RECRUITINGStage 1: MTD (Maximum tolerated dose)or RP2D(Recommended Phase II Dose) of SHR1459 and YY-20394;
Time frame: Minimum observation period is 28 days for the maximum dose cohort
Stage 2: Overall response rate (ORR)
Time frame: 8 weeks after last patient first visit (LPFV)
Incidence of Adverse Events
Time frame: At every treatment and follow up visit until disease progression. Expected to be for up to 6 months
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