Try the modernized beta website. Learn more about the modernization effort.
Working… Menu

Comparative Study of the Effect of Ezetimibe Versus Extended-Release Niacin on Atherosclerosis

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00397657
Recruitment Status : Terminated (Independent steering committee has stopped the trial based on results of a prespecified, blinded interim analysis. It was not stopped due to safety concerns.)
First Posted : November 9, 2006
Last Update Posted : June 17, 2009
Information provided by:
Walter Reed Army Medical Center

Brief Summary:

Recent evidence on the use of statin therapy indicates the potential for ultra-low levels of low-density lipoprotein (LDL-C) to provide greater protection from recurrent coronary heart disease (CHD) events. Thus, in August 2005, the guidelines for the treatment of lipid disorders (NCEP ATPIII) were revised to indicate that an LDL-C treatment goal of 70 mg/dL (revised from 100 mg/dL) was optional for patients with known CHD. In these same guidelines, low levels of high-density lipoprotein (HDL-C) are also suggested but not specifically proscribed as a target of therapy. Recently the ARBITER 2 trial has provided the first evidence of the potential of raising HDL-C with extended release niacin when added to statin monotherapy. However, whether this approach would be superior to a strategy in which lower concentrations of LDL-C are targeted is unknown.

The purpose of ARBITER 6 - HALTS is to compare HDL and LDL-focused strategies of lipid treatments for their effects of atherosclerosis. This study is a prospective, randomized, open-label, blinded endpoint trial comparing treatment strategies of either HDL-raising therapies or LDL reduction for dyslipidemia on carotid atherosclerosis. Subjects with known atherosclerotic coronary or vascular disease or otherwise at high cardiovascular risk through the presence of a coronary risk equivalent who are currently being treated with a statin will be eligible. Subjects will be randomly assigned in an allocation-concealed fashion to open label treatment with either Ezetimibe 10 mg/d for additional LDL-lowering OR Extended-release niacin (1 gm/d, titrated to max tolerable dose up to 2 gm/d) for HDL improvement.

The effects of these 2 different strategies of intensified lipid management on atherosclerosis will be assessed by the change in the carotid intima-media thickness, a validated surrogate endpoint. The data will help guide clinicians on the potential benefits of these lipid treatment strategies.

Condition or disease Intervention/treatment Phase
Atherosclerosis Drug: extended release niacin Drug: ezetimibe Phase 4

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 400 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: ARBITER 6: ARterial Biology for the Investigation of the Treatment Effects of Reducing Cholesterol 6 - HDL and LDL Treatment Strategies in Atherosclerosis (HALTS)
Study Start Date : November 2006
Estimated Primary Completion Date : August 2009
Estimated Study Completion Date : October 2009

Resource links provided by the National Library of Medicine

Arm Intervention/treatment
Active Comparator: Extended release niacin Drug: extended release niacin
Extended release niacin will be started at 1000mg and titrated to 2000mg once a day

Drug: ezetimibe
Ezetimibe 10mg once daily

Active Comparator: Ezetimibe Drug: ezetimibe
Ezetimibe 10mg once daily

Primary Outcome Measures :
  1. The primary endpoint is the change in carotid intima-media thickness between groups after 14 months [ Time Frame: 14 months ]

Secondary Outcome Measures :
  1. The change in lipid values and lipid subfractions [ Time Frame: 14 months ]
  2. A composite endpoint consisting of all major adverse cardiovascular events (coronary heart disease death, myocardial infarction, myocardial revascularization, admission to the hospital for an acute coronary syndrome) [ Time Frame: 14 months ]
  3. Drug discontinuation due to adverse effects [ Time Frame: 14 months ]
  4. Quality of life measured with the EQ-5D questionnaire- a generic questionnaire for describing and valuing subjects' health-related quality of life that has been studied in cardiovascular subjects [ Time Frame: 14 months ]

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Layout table for eligibility information
Ages Eligible for Study:   30 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Male and female subjects, ≥ 30 years old with either known atherosclerotic coronary or vascular disease OR coronary risk equivalents defined as either:

    • diabetes mellitus,
    • multiple coronary risk factors with a Framingham Risk Score > 2% per year, or
    • an elevated coronary calcium score (> 400 for men, > 200 for women)
  • Currently being treated with a statin (Simvastatin 20 mg/d or its equivalent) as monotherapy for treatment of hyperlipidemia
  • Recent lipids (within the past 3 months without interval change in the statin regimen) showing both: LDL-C < 100 mg/dL and HDL-C < 50 mg/dL (men) or < 55 mg/dL (women)

Exclusion Criteria:

  • Current use of or known intolerance to niacin or ezetimibe
  • Known history of liver disease (cirrhosis, chronic hepatitis) or abnormal liver associated enzymes, > 3x the upper laboratory reference value
  • Enrollment in another drug or device research protocol
  • Females who are pregnant, expect to get pregnant during the course of the study, or are breastfeeding

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00397657

Layout table for location information
United States, District of Columbia
Walter Reed Army Medical Center
Washington, District of Columbia, United States, 20307
United States, Maryland
Washington Adventist Hospital
Takoma Park, Maryland, United States, 20912
Sponsors and Collaborators
Walter Reed Army Medical Center
Layout table for investigator information
Principal Investigator: Allen J Taylor, MD Medstar Research Institute and Washington Hospital Center, Washington DC.

Publications automatically indexed to this study by Identifier (NCT Number):
Layout table for additonal information
Responsible Party: Allen J Taylor, MD, Medstar Research Institute and Washington Hospital Center, Washington DC Identifier: NCT00397657    
Other Study ID Numbers: 06-12027
First Posted: November 9, 2006    Key Record Dates
Last Update Posted: June 17, 2009
Last Verified: June 2009
Keywords provided by Walter Reed Army Medical Center:
carotid intima media thickness
coronary heart disease
Additional relevant MeSH terms:
Layout table for MeSH terms
Arterial Occlusive Diseases
Vascular Diseases
Cardiovascular Diseases
Anticholesteremic Agents
Hypolipidemic Agents
Molecular Mechanisms of Pharmacological Action
Lipid Regulating Agents
Vasodilator Agents
Vitamin B Complex
Physiological Effects of Drugs