The purpose of this study is to evaluate the safety and effectiveness of the combination of bendamustine and ofatumumab in subjects with relapsed/refractory chronic lymphocytic leukemia and small cell lymphoma. All subjects enrolled on this study will receive both drugs by intravenous (IV) infusion.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
10
Ofatumumab 300-mg IV on Day 1 of week -1 and then 1000 mg on Day 1 of each cycle for 6 cycles Bendamustine 70 mg/m2 IV on days 1 and 2 of each cycle for 6 cycles
Georgetown University
Washington D.C., District of Columbia, United States
Overall Response Rate
40% per the National Cancer Institute Working Group Response Criteria for Chronic Lymphocytic Leukemia
Time frame: 6 months
Complete Response Rate
NCI IWG response criteria
Time frame: 6 months
Median PFS
Kaplan Meyer PFS
Time frame: 2 years
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