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Safety & Efficacy of a Combination Niacin ER/Simvastatin in Patients With Dyslipidemia: A Dose-Ranging Study - SEACOAST
This study has been completed.
Study NCT00082251   Information provided by Kos Pharmaceuticals
First Received: May 3, 2004   Last Updated: October 31, 2006   History of Changes

May 3, 2004
October 31, 2006
 
 
 
 
Complete list of historical versions of study NCT00082251 on ClinicalTrials.gov Archive Site
 
 
 
Safety & Efficacy of a Combination Niacin ER/Simvastatin in Patients With Dyslipidemia: A Dose-Ranging Study - SEACOAST
Safety & Efficacy of a Combination Niacin ER/Simvastatin in Patients With Dyslipidemia: A Dose-Ranging Study - SEACOAST

The purpose of this study is to compare the effectiveness and safety of different doses of Niacin ER/Simvastatin (NS), in subjects with elevated fat levels in their blood (dyslipidemia).

The purpose of this study is to compare the efficacy and safety of different doses of Niacin ER/Simvastatin (NS), in subjects with elevated fat levels in their blood (dyslipidemia).

Phase III
Interventional
Treatment, Randomized, Double-Blind, Active Control, Parallel Assignment, Safety/Efficacy Study
Hypercholesterolemia
Drug: Niacin extended release and simvastatin tablets
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
 
 
 

Inclusion Criteria:

  • Patient has primary Type II hyperlipidemia or mixed dyslipidemia
  • If the patient is currently taking anti-dyslipidemic medications other than Zocor, he/she is willing to withdraw from these medications
  • Reasonable compliance with a standard cholesterol-lowering diet for a minimum of 4 weeks prior to screening and for the duration of the study.
  • LDL-C levels and/or Non HDL-C levels above normal for patients

This study will be conducted both in the USA and internationally.

Exclusion Criteria:

  • Patient has an allergy, hypersensitivity, or intolerance to niacin, statins, or their derivatives
  • HbA1c ≥ 9% in diabetic patients
Both
21 Years and older
No
Contact information is only displayed when the study is recruiting subjects
 
 
NCT00082251
 
019-01-03-CR, SEACOAST
Kos Pharmaceuticals
 
 
Kos Pharmaceuticals
October 2006

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP