This study is to compare its pharmacokinetics profile of two YM150 formulations by 2x2 crossover method.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
NONE
Enrollment
44
oral
Unnamed facility
Kyushu, Japan
Plasma concentration of YM150 and its metabolites measured by blood sample
Time frame: for 3 days after drug administration
Safety assessed by AEs, vital signs, 12-lead ECG and lab tests
Time frame: or 3 days after drug administration
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