The primary objective of this clinical research study is to evaluate the safety, tolerability, and maximum tolerated dose (MTD) of intravenous (IV) MST-997 formulated in Intralipid 20% administered on a weekly schedule to subjects with advanced malignant solid tumors.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Unnamed facility
New York, New York, United States
Unnamed facility
Cleveland, Ohio, United States
Unnamed facility
Nashville, Tennessee, United States
To evaluate the safety, tolerability and MTD of IV MST-997 throughout patients participation on trial.
To obtain preliminary information on the pharmacokinetics (during cycle 1) and antitumor activity of MST-997 (approximately every 8 weeks).
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