The primary objective of the study is to determine the safety profile and overall response rate of IPI 504 in patients with advanced dedifferentiated liposarcoma.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
IPI 504 administered twice weekly at 225 mg/m2 for 2 weeks followed by 1 week off treatment
Dana-Farber Cancer Institute
Boston, Massachusetts, United States
To determine the safety profile and overall response rate (ORR) of IPI 504 in patients with advanced dedifferentiated liposarcoma.
Time frame: Every 6 weeks
To determine the clinical benefit rate and duration of overall response
Time frame: Every 6 weeks
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