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Effect Of Rilapladib (SB-659032) On Platelet Aggregation

A Double Blind, Placebo Controlled, Parallel Study to Evaluate Effects of Repeat Doses of Rilapladib on Platelet Aggregation in Healthy Male Volunteers

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00387257
Enrollment
58
Registered
2006-10-12
Start date
2006-10-31
Completion date
2007-04-30
Last updated
2015-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atherosclerosis, Healthy Subjects

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
Lead SponsorINDUSTRY

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

MeasureTime 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

MeasureTime 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

Source: ClinicalTrials.gov · Data processed: Mar 8, 2026