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Efficacy and Safety Study of Fluvastatin and Ezetimibe Combined Versus Fluvastatin Alone

This study has been completed.

Sponsored by: Novartis
Information provided by: Novartis
ClinicalTrials.gov Identifier: NCT00171288
  Purpose

The objective of this study is to assess the effect of the combination treatment on C-reactive protein and inflammatory markers as well as the safety and tolerability in a Spanish population


Condition Intervention Phase
Dyslipidemia
Drug: fluvastatin, ezetimibe
Phase III

MedlinePlus related topics:   Cholesterol   

Drug Information available for:   Ezetimibe    Fluvastatin   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Safety/Efficacy Study
Official Title:   Efficacy and Safety Study of Fluvastatin and Ezetimibe Combined Versus Fluvastatin Alone

Further study details as provided by Novartis:

Primary Outcome Measures:
  • Change from baseline in low density lipoprotein cholesterol after 12 weeks

Secondary Outcome Measures:
  • Change from baseline in total triglyceride, high density lipoprotein cholesterol, and composition of low density lipoprotein cholesterol after 12 weeks
  • Change from baseline in circulating marker of inflammation after 12 weeks

Estimated Enrollment:   80
Study Start Date:   August 2003

  Eligibility
Ages Eligible for Study:   18 Years to 75 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

Inclusion Criteria:

  • Patients aged 18-75 Primary hypercholesterolemia Signed informed consent

Exclusion Criteria:

  • Patients involved in clinical trials 3 months prior to inclusion Patients treated with drugs specified in protocol Fertile women not using contraceptive methods

Other protocol defined in and exclusion criteria may apply

  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00171288

Locations
Spain
Novartis    
      Madrid, Spain

Sponsors and Collaborators
Novartis

Investigators
Study Director:     Novartis Pharmaceuticals     Novartis Pharmaceuticals    
  More Information


Study ID Numbers:   CXUO320BES03
First Received:   September 12, 2005
Last Updated:   March 20, 2008
ClinicalTrials.gov Identifier:   NCT00171288
Health Authority:   Spain: Spanish Agency of Medicines

Keywords provided by Novartis:
Dyslipidemia, ezetimibe, inflammatory markers, fluvastatin  

Study placed in the following topic categories:
Metabolic Diseases
Ezetimibe
Metabolic disorder
Fluvastatin
Dyslipidemias
Lipid Metabolism Disorders

Additional relevant MeSH terms:
Antimetabolites
Molecular Mechanisms of Pharmacological Action
Therapeutic Uses
Antilipemic Agents
Enzyme Inhibitors
Anticholesteremic Agents
Hydroxymethylglutaryl-CoA Reductase Inhibitors
Pharmacologic Actions

ClinicalTrials.gov processed this record on November 06, 2008




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