A study to evaluate safety and tolerability of MK6592 in combination with an anti-cancer drug in adult patients with advanced solid tumors.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
38
MK6592 delivered as a 48-hour CIV as monotherapy in Cycle 1; 48-hour CIV of MK6592 in Cycle 2 and subsequent cycles.
docetaxel, delivered as a standard IV infusion.
Safety and tolerability of MK6592 alone and in combination with docetaxel
Time frame: 6 Months
Observance of objective tumor responses in patients treated with MK6592 combined with docetaxel
Time frame: 6 Months
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