Phase 1, open-labeled, safety and tolerability study for the treatment of subjects with relapsed or refractory solid tumors.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
55
IV infusion once every 3 weeks until disease progression or unacceptable toxicity
Research Site
Santa Monica, California, United States
Research Site
Philadelphia, Pennsylvania, United States
Research Site
San Antonio, Texas, United States
To evaluate safety
Time frame: ongoing
To determine the maximum-tolerated dose (MTD)
Time frame: ongoing
To evaluate pharmacokinetics (PK)
Time frame: ongoing
To evaluate clinical activity
Time frame: ongoing
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