This is a Phase I, first-in-human, open-label, dose-escalation study of MNRP1685A administered by IV infusion every 3 weeks in patients with locally advanced or metastatic solid tumors for whom standard therapy either does not exist or has proven to be ineffective or intolerable. This study will be conducted at up to three study centers in the United States.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
35
Escalating intravenous dose
Incidence and nature of dose-limiting toxicities (DLTs)
Time frame: Length of study
Total exposure (AUC)
Time frame: Length of study
Maximum and minimum serum concentrations
Time frame: Length of study
Clearance
Time frame: Length of study
Volume of distribution
Time frame: Length of study
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