To evaluate the safety and plasma concentration change of YM178 after single- and repeated-administration as oral absorption controlled tablet in healthy Chinese subjects.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Masking
NONE
Enrollment
24
oral
Unnamed facility
Shanghai, China
AUC of YM178 assessed by the plasma concentration changes
Time frame: Up to 96 hours after administration
Cmax of YM178 assessed by the plasma concentration changes
Time frame: Up to 96 hours after administration
t1/2 of YM178 assessed by the plasma concentration changes
Time frame: Up to 96 hours after administration
Safety assessment of YM178
Safety is to be assessed by the incidence of adverse events, vital signs, lab-tests and 12-lead ECGs
Time frame: Up to 33 days
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