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Completed Phase 2 Interventional

Efficacy and Safety of the ACAT Inhibitor CS-505 (Pactimibe) for Reducing the Progression of Coronary Artery Disease

ClinicalTrials.gov ID: NCT00185042

Public ClinicalTrials.gov record NCT00185042. 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 Apr 29, 2026, 9:44 AM 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 Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study of the Efficacy and Safety of the ACAT Inhibitor CS-505 for Reducing the Progression of Atherosclerosis in Subjects With Coronary Artery Disease Using Intravascular Ultrasound (IVUS)

Study identification

NCT ID
NCT00185042
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Daiichi Sankyo
Industry
Enrollment
534 participants

Conditions and interventions

Interventions

  • Pactimibe, CS-505 Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Oct 31, 2002
Primary completion
Not listed
Completion
Jun 30, 2005
Last update posted
Sep 10, 2007

2002 – 2005

United States locations

U.S. sites
46
U.S. states
23
U.S. cities
46
Facility City State ZIP Site status
Not listed Birmingham Alabama
Not listed Huntsville Alabama
Not listed Mobile Alabama
Not listed Phoenix Arizona
Not listed Los Angeles California
Not listed San Diego California
Not listed Fort Collins Colorado
Not listed Bridgeport Connecticut
Not listed Newark Delaware
Not listed Clearwater Florida
Not listed Gainsville Florida
Not listed Hudson Florida
Not listed Jacksonville Florida
Not listed Melbourne Florida
Not listed Miami Florida
Not listed Pensacola Florida
Not listed Port Charlotte Florida
Not listed Sarasota Florida
Not listed Tallahassee Florida
Not listed Tampa Florida
Not listed Atlanta Georgia
Not listed Springfield Illinois
Not listed Louisville Kentucky
Not listed Baltimore Maryland
Not listed Springfield Massachusetts
Not listed Grand Rapids Michigan
Not listed Kalamazoo Michigan
Not listed Duluth Minnesota
Not listed Minneapolis Minnesota
Not listed Kansas City Missouri
Not listed Lincoln Nebraska
Not listed New York New York
Not listed Rochester New York
Not listed Troy New York
Not listed Charlotte North Carolina
Not listed Greenville North Carolina
Not listed High Point North Carolina
Not listed Winston-Salem North Carolina
Not listed Akron Ohio
Not listed Cleveland Ohio
Not listed Elyria Ohio
Not listed Mansfield Ohio
Not listed Oklahoma City Oklahoma
Not listed Doylestown Pennsylvania
Not listed Memphis Tennessee
Not listed San Antonio Texas

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 NCT00185042, 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 Sep 10, 2007 · Synced Apr 29, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00185042 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →