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Completed

NCT Number: NCT00474240

AEGR-733 and Atorvastatin 20 mg vs. Monotherapy in Moderate Hypercholesterolemia

The purpose of this study is to test the effectiveness of the study drug, AEGR-733 alone and in combination with the medication, atorvastatin (Lipitor), on cholesterol in volunteers with moderately high cholesterol.

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Medical Affiliated Research Center, Huntsville, Alabama, United States

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About this study

Recent studies suggest more intensive cholesterol lowering treatment for people at very high risk of a heart attack, specifically for patients who have heart disease plus major risk factors. Available medications used alone at even the highest approved doses are not expected to reach these new target recommendations for cholesterol in a large number of subjects. Thus, the development of new medications that can provide additional cholesterol lowering may be beneficial.

This study tests the effectiveness of different doses of the study drug, AEGR-733 alone and in combination with the approved cholesterol lowering drug, atorvastatin (Lipitor), on cholesterol. Volunteers will be randomized to one of 6 different study treatments and will take the assigned medication (3 capsules daily) for 8 weeks.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Men and women between the ages of 18 and 70 years.
  • Elevated LDL cholesterol based on risk factors for cardiovascular disease or presence of cardiovascular disease

Exclusion criteria

  • Women who are pregnant, lactating, planning to become pregnant, or women of childbearing potential who have not successfully been using acceptable contraceptive methods over the previous 3 months, e.g., intrauterine device (IUD) and barrier method plus spermicide.
  • Uncontrolled hypertension
  • History of chronic kidney problems
  • History of liver disease
  • Positive for Hepatitis B or Hepatitis C.
  • Any major surgical procedure occurring less than 3 months ago
  • Cardiac insufficiency
  • History of a malignant cancer (other than basal cell or squamous cell carcinoma of the skin that has been removed) within the previous 5 years.
  • Regular alcohol use >1 drink per day.
  • Regular consumers of grapefruit juice, or currently taking the following medications: cyclosporine, itraconazole, ketoconazole, erythromycin, clarithromycin, telithromycin, HIV protease inhibitors, and nefazodone.
  • Use of other cholesterol lowering medications that cannot be stopped.
  • Heart attack or stroke within the previous 6 months
  • Diabetes Mellitus
  • Body mass index (BMI) ≥ 40 kg/m2.
  • Significant gastrointestinal symptoms, such as irritable bowel syndrome.
  • Current use of fish oils, niacin, and herbal weight loss products that cannot be stopped.

Treatment and study plan

Atorvastatin 20 mg

Drug

AEGR-733 5 mg

Drug

AEGR-733 10 mg

Drug

Placebo

Drug

AEGR-733 5 mg + atorvastatin 20 mg

Drug

AEGR-733 10 mg + atorvastatin 20 mg

Drug

Primary outcomes

  1. Percent Change From Baseline in LDL-C at 8 Weeks

    Time frame: Atfer 8 weeks on study drug

Secondary outcomes

  1. Percent Change From Baseline of Other Lipids

    Time frame: After 8 weeks of study drug

Sponsors and collaborators

Lead sponsor

Aegerion Pharmaceuticals, Inc.

Industry

Registry information

Official study title

A Randomized, Double-blind, Placebo-controlled, Parallel Group Study to Evaluate the Safety and Efficacy of the Combination of AEGR-733 (Formerly BMS201038) and Atorvastatin 20 mg vs. Monotherapy in Subjects With Moderate Hypercholesterolemia

Important dates

Study start
2007
Primary completion
2008
Study completion
2008
First posted
May 16, 2007
Registry last updated
Mar 20, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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