A study to determine the safety, tolerability, and anti-tumor effectiveness of an oral investigational drug in the treatment of relapsed diffuse large B-cell lymphoma.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
18
Objective response rate based on FDG-PET and CT scan findings.
Response duration, Progression-free survival, Time to progression, Time to response, 3-Month and 6-month progression free survival.
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