Atherosclerosis, Healthy Subjects
Conditions
Keywords
platelet aggregation, SB-659032, rilapladib
Brief summary
The purpose of this study is to compare the effects of repeat doses of SB-659032 with placebo on platelet aggregation in subjects.
Interventions
DRUGRilapladib (SB-659032)
Sponsors
GlaxoSmithKline
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
DOUBLE
Eligibility
Sex/Gender
MALE
Age
18 Years to 55 Years
Healthy volunteers
Yes
Inclusion criteria
* Subjects with QTc \< 450 msec as measured at screening.
Exclusion criteria
* History of asthma. * Smokers.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Collagen EC50 values on Day 35 (or 21 days post last dose) as determine by optical aggregometry. | on Day 35 (or 21 days post last dose) as determine by optical aggregometry |
Secondary
| Measure | Time frame |
|---|---|
| Collagen EC50 values on Day 1 and Day 14 as determined by optical aggregometry Plasma Lp-PLA2 activity Clinical safety data Concentrations of rilapladib and SB-664601. | on Day 1 and Day 14 as determined by optical aggregometry |
Countries
Australia
Outcome results
None listed