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COMPLETED Phase 2

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

NCT00695305 · View on ClinicalTrials.gov ↗

Study Summary

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

Conditions Studied

Interventions

  • DRUG placebo
  • DRUG rilapladib
  • OTHER 18F Fluorodeoxylucose (FDG)-PET

Study Locations (10)

New York

  • GSK Investigational Site — New York
  • GSK Investigational Site — New York
  • GSK Investigational Site — New York
  • GSK Investigational Site — New York
  • GSK Investigational Site — North Massapequa

Massachusetts

  • GSK Investigational Site — Boston
  • GSK Investigational Site — Brockton
  • GSK Investigational Site — Haverhill

New Jersey

  • GSK Investigational Site — Linden

Rhode Island

  • GSK Investigational Site — Warwick

Trial Details

FieldValue
Enrollment Target 83 participants
Start Date 2008-11
Est. Completion 2010-05
Phase Phase 2

Sponsor

GlaxoSmithKline

558 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00695305

The ClinicalTrials.gov registry entry for NCT00695305 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 83 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is GlaxoSmithKline, which has 558 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Atherosclerosis appearing as the primary indexed condition, and to 3 interventions — of which placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00695305 reports 10 study locations spanning 4 distinct geographic areas — top geographies include New York, Massachusetts, New Jersey. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00695305 about?

NCT00695305 is a clinical study titled "An Imaging Study in Patients With Atherosclerosis Taking Rilapladib or Placebo for 12 Weeks". A study in patients with atherosclerosis to assess safety, effect and PK of rilapladib vs. placebo over 12 weeks of dosing.

What is the current status of trial NCT00695305?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 83 participants. The study started on 2008-11. Estimated completion is 2010-05.

What conditions does trial NCT00695305 study?

This clinical trial studies the following conditions: Atherosclerosis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00695305?

The interventions under investigation include: placebo (DRUG), rilapladib (DRUG), 18F Fluorodeoxylucose (FDG)-PET (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00695305?

This trial is sponsored by GlaxoSmithKline, which has 558 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00695305 being conducted?

This trial has 10 study locations across Massachusetts, New Jersey, New York, Rhode Island. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial