This is an open label, randomized phase II study designed to evaluate the tolerability and response rate of high-dose and low-dose regimens in patients with advanced cutaneous T-cell lymphoma (CTCL).
This is an open label, randomized phase II study designed to evaluate the tolerability and response rate of high-dose and low-dose regimens in patients with advanced cutaneous T-cell lymphoma (CTCL) who have had progressive, recurrent, or persistent disease on or following 2 systemic therapies.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
16
Sapacitabine
Stanford University Hospitals and Clinics
Stanford, California, United States
Timothy Kuzel, M.D.
Chicago, Illinois, United States
The University of Texas MD Anderson Cancer Center
Houston, Texas, United States
response rate in overall skin disease
Decrease of lesion from baseline
Time frame: over the course of study
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