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Terminated Phase 3 Interventional Results available

A Study of the Effect of Dalcetrapib on Artherosclerotic Disease in Patients With Coronary Artery Disease

ClinicalTrials.gov ID: NCT01059682

Public ClinicalTrials.gov record NCT01059682. 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 Nov 8, 2026, 2:17 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multi-Center, Double-blind, Randomized, Placebo Controlled, Parallel Group Study of the Effect of Dalcetrapib on Atherosclerotic Disease Progression As Measured by Coronary Intravascular Ultrasound, Carotid B-Mode Ultrasound and Coronary Angiography

Brief summary

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

This multicenter, double-blind, randomized, placebo-controlled study will evaluate the effect of dalcetrapib 600 mg on artherosclerotic disease progression, lipid profile and biomarker profile and long-term safety profile of dalcetrapib in patients with coronary artery disease. Atherosclerotic disease progression will be measured 1. Coronary Intravascular Ultrasound (IVUS), Quantitative Coronary Angiography 2. Carotid B-Mode Ultrasound Intima Medial Thickness (IMT) and total plaque volume in subjects undergoing coronary angiography who have coronary artery disease (CAD). Patients will be randomized to receive dalcetrapib 600 mg orally once a day or placebo. The anticipated time on study treatment will be 24 months. The target sample size is 800-1000 patients.

Study identification

NCT ID
NCT01059682
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
936 participants

Conditions and interventions

Interventions

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
Jan 2010 (Type not available)
Primary completion
Sep 2011 (Actual)
Completion
Sep 2011 (Actual)
Last update posted
Mar 24, 2020

2010 – 2011

United States locations

U.S. sites
41
U.S. states
22
U.S. cities
39
Facility City State ZIP Site status
Not listed Los Angeles California 90033 —
Not listed Los Angeles California 90073 —
Not listed Torrance California 90502 —
Not listed Boulder Colorado 80304 —
Not listed Greeley Colorado 80631 —
Not listed Littleton Colorado 80120 —
Not listed Hartford Connecticut 06115 —
Not listed Atlantis Florida 33462 —
Not listed Fort Lauderdale Florida 33308 —
Not listed Fort Lauderdale Florida 33316 —
Not listed Jacksonville Florida 32216 —
Not listed Miami Florida 33137 —
Not listed Sarasota Florida 34239 —
Not listed Tampa Florida 33609 —
Not listed Decatur Georgia 30033 —
Not listed Chicago Illinois 60637-1470 —
Not listed Elkhart Indiana 46514 —
Not listed Louisville Kentucky 40205 —
Not listed Columbia Maryland 21044 —
Not listed Salisbury Maryland 21804 —
Not listed Boston Massachusetts 02114 —
Not listed Ann Arbor Michigan 48109-0666 —
Not listed Kalamazoo Michigan 49048 —
Not listed Midland Michigan 48670 —
Not listed Muskegon Michigan 49444 —
Not listed Petoskey Michigan 49770 —
Not listed Duluth Minnesota 55805 —
Not listed Rochester Minnesota 55905 —
Not listed Kansas City Missouri 64114 —
Not listed Paramus New Jersey 07652 —
Not listed New York New York 10011 —
Not listed Rochester New York 14642 —
Not listed Chapel Hill North Carolina 27599 —
Not listed Toledo Ohio 43614 —
Not listed Hershey Pennsylvania 17033 —
Not listed Providence Rhode Island 02906 —
Not listed Germantown Tennessee 38138 —
Not listed Oak Ridge Tennessee 37830 —
Not listed Dallas Texas 75216 —
Not listed Houston Texas 77030 —
Not listed Richmond Virginia 23249 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 69 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01059682, 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 Mar 24, 2020 · Synced Nov 8, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01059682 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →