The purpose of this study is to determine the safety, maximum tolerated dose and pharmacokinetics of IPI-145 in patients with advanced hematologic malignancies.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
210
Oral Twice A Day (BID) Dosing
Unnamed facility
New York, New York, United States
Unnamed facility
Columbus, Ohio, United States
Unnamed facility
Nashville, Tennessee, United States
Unnamed facility
Houston, Texas, United States
Safety and Tolerability
To determine the incidence of adverse events and abnormal laboratory test results, including dose-limiting toxicities.
Time frame: At least 28 days (1 Cycle)
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