This is a first-in-man study to assess the safety and tolerability and to characterise the pharmacokinetics of ODM-207.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
36
Helsinki University Central Hospital, Department of Oncology
Helsinki, Finland
Maximum Tolerated Dose
Highest dose level at which \<33% of patients in a cohort experience Dose Limiting Toxicity (DLT)
Time frame: 28 days
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