Safety Study of BMS-823778 in Subjects With Hypercholesterolemia



Status:Completed
Conditions:High Cholesterol, High Cholesterol
Therapuetic Areas:Cardiology / Vascular Diseases
Healthy:No
Age Range:18 - 75
Updated:4/21/2016
Start Date:June 2010
End Date:December 2010

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A Double-Blind, Placebo-Controlled, Parallel-Group, Randomized, Multiple Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamic Effects of BMS-823778 in Non-Diabetic Subjects With Primary Hypercholesterolemia on a Stable Dose of Statin Therapy With or Without Ezetimibe

The purpose of this study is to assess the safety, tolerability and pharmacodynamic effects
on LDL cholesterol (LDL-C)


Inclusion Criteria:

- Hypercholesterolemia

- Currently taking a stable daily dose of statin therapy

- Serum triglyceride level < 500mg/dl

Exclusion Criteria:

- History of myocardial infarction, coronary angioplasty or bypass grafts, valvular
disease or repair, unstable angina pectoris, transient ischemic attack, or
cerebrovascular accidents within six months prior to entry into the study

- Congestive heart failure

- Diabetes mellitus

- Active liver disease

- Impaired renal function

- Hepatitis C, B and HIV

This list is not inclusive; additional information is provided in the protocol
We found this trial at
7
sites
Little Rock, Arkansas 72201
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Brisbane, Queensland
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Brisbane,
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Cincinnati, Ohio 45219
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Cincinnati, OH
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Lenexa, Kansas 66219
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Lenexa, KS
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Norfolk, VA
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Richmond, VA
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San Antonio, Texas 78229
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San Antonio, TX
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