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Completed Phase 2 Interventional

An Imaging Study in Patients With Atherosclerosis Taking Rilapladib or Placebo for 12 Weeks

ClinicalTrials.gov ID: NCT00695305

Public ClinicalTrials.gov record NCT00695305. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 6:56 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, 12 Week, Double-blind, Placebo-controlled, Parallel-group, Phase IIa Study Using 18F Fluorodeoxyglucose (FDG)-PET to Measure the Effects of Rilapladib on Macrophage Activity in Subjects With Atherosclerosis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

A study in patients with atherosclerosis to assess safety, effect and PK of rilapladib vs. placebo over 12 weeks of dosing.

Study identification

NCT ID
NCT00695305
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
83 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
50 Years to 80 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 2008 (Type not available)
Primary completion
May 2010 (Actual)
Completion
May 2010 (Actual)
Last update posted
Dec 1, 2016

2008 – 2010

United States locations

U.S. sites
10
U.S. states
4
U.S. cities
7
Facility City State ZIP Site status
GSK Investigational Site Boston Massachusetts 02114 —
GSK Investigational Site Brockton Massachusetts 02301 —
GSK Investigational Site Haverhill Massachusetts 01830 —
GSK Investigational Site Linden New Jersey 07036 —
GSK Investigational Site New York New York 10001 —
GSK Investigational Site New York New York 10029 —
GSK Investigational Site New York New York 10035 —
GSK Investigational Site New York New York 10065 —
GSK Investigational Site North Massapequa New York 11758 —
GSK Investigational Site Warwick Rhode Island 02886 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00695305, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 1, 2016 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00695305 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →