This study is being conducted to provide initial safety, tolerability, PK and PD data that will allow further studies with darapladib in Japanese patients
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
18
GSK Investigational Site
Honolulu, Hawaii, United States
- Safety/tolerability of single oral doses of darapladib
Time frame: 4, 24 and 96h post-dose
- Primary Pharmacokinetic parameters of single oral doses of darapladib
Time frame: pre-dose, 0,5, 1, 2, 3, 4, 6, 9 12, 16, 24, 48, 72h post-dose
-Secondary PK parameters -PK parameters of SB553253 -inhibition of Lp-PLA2 activity -description of plasma concentration-Lp-PLA2 activity inhibition relationship after single oral doses of darapladib. all measured same timepoints as primary PK
Time frame: Throughout the study
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