The purpose of this study is to evaluate the pharmacokinetics profile and drug-drug interaction between amlodipine, olmesartan and rosuvastatin in healthy adult volunteers.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
NONE
Enrollment
32
Treatment AB
Treatment AB/Treatment C
Samsung medical center
Seoul, South Korea
AUCtau
Time frame: Multiple blood sample will be collected for 24 hours after last dosing in each of the treatment
Css,max
Time frame: Multiple blood sample will be collected for 24 hours after last dosing in each of the treatment
Tss,max
Time frame: Multiple blood sample will be collected for 24 hours after last dosing in each of the treatment
Css,min
Time frame: Multiple blood sample will be collected for 24 hours after last dosing in each of the treatment
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