In this study participants with relapsed/refractory leukemia will be given MK-0457 in sequential cohorts and with varying treatment duration to determine the maximum tolerated dose (MTD) for MK-0457.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
28
Number of Participants Experiencing Dose-Limiting Toxicities (DLTs)
Time frame: Part 1: up to 5 days, Part 2: up to 24 hours
Hematological response rate to MK-0457 as a 5-day CIV infusion
Time frame: At the end of each cycle (up to 18 months)
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