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Completed Phase 2 Interventional Results available

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

ClinicalTrials.gov ID: NCT00474240

Public ClinicalTrials.gov record NCT00474240. 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 Jul 23, 2026, 2:11 PM 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 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

Study identification

NCT ID
NCT00474240
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Aegerion Pharmaceuticals, Inc.
Industry
Enrollment
157 participants

Conditions and interventions

Interventions

  • 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

Drug

Eligibility (public fields only)

Age range
18 Years to 70 Years
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
Mar 31, 2007
Primary completion
Sep 30, 2008
Completion
Sep 30, 2008
Last update posted
Mar 19, 2018

2007 – 2008

United States locations

U.S. sites
17
U.S. states
12
U.S. cities
15
Facility City State ZIP Site status
Medical Affiliated Research Center Huntsville Alabama 35801
Jacksonville Center for Clinical research Jacksonville Florida 32205
Jacksonville Center For Clinical Research Jacksonville Florida 32216
Renstar Medical Research Ocala Florida 34471
North Georgia Clinical Research Woodstock Georgia 30189
Radiant Research Chicago Illinois 60610
Medsphere Medical Research Center Evansville Indiana 47714
Midwest Institute for Clinical Research Indianapolis Indiana 46260
Maine Research Associates Auburn Maine 04210
Health Trends Research Baltimore Maryland 21209
Piedmont Medical Research Associates Winston-Salem North Carolina 27103
Sterling Research Group Cincinnati Ohio 45246
Coastal Carolina Research Center Goose Creek South Carolina 29445
Dallas Diabetes and Endocrine Center Dallas Texas 75230
Diabetes and Glandular Disease Research Dallas Texas 78229
Hampton Roads Center for Clinical Research Norfolk Virginia 23502
National Clinical Research Richmond Virginia 23294

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 NCT00474240, 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 19, 2018 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00474240 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →