This study will provide an initial assessment of the safety, tolerability, and pharmacokinetics (PK) of PAZ-417 after administration of ascending single oral doses to healthy young Japanese male and healthy elderly Japanese male subjects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
56
Unnamed facility
Kitashinagawa, Shinagawa-ku, Tokyo, Japan
Safety and Tolerability
Time frame: 3 months
Pharmacokinetics
Time frame: 3 months
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