The purpose of the study is to evaluate the safety and tolerability of ASP1517 after single or multiple oral administration in healthy non-elderly adult male subjects.
The study consists of two parts, single and multiple dose. Within each part participants will be randomized to either ASP1517 or placebo.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
SINGLE
Enrollment
100
Unnamed facility
Kantou, Japan
Safety and tolerability of ASP1517
Time frame: During 2 weeks
Pharmacokinetics of ASP1517
Time frame: During 2 weeks
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