The purpose of this study is to evaluate the safety and effectiveness of auranofin to treat patients with chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), or prolymphocytic lymphoma (PLL).
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
15
6 mg twice a day for a total of 12 mg total daily dose
University of Kansas Cancer Center
Westwood, Kansas, United States
Response Rate
Time frame: 24 months
type, incidence, severity, seriousness and relationship to auranofin of adverse events and any laboratory abnormalities
Time frame: 24 months
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