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Clinical Trial Summary

The purpose of this study is to compare the efficacy of pitavastatin with that of atorvastatin.


Clinical Trial Description

Following a wash-out dietary lead-in period, patients will receive either Atorvastatin or Pitavastatin during 12 weeks, in order to establish the efficacy of pitavastatin in reducing cholesterol levels. ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00249249
Study type Interventional
Source Kowa Research Europe
Contact
Status Completed
Phase Phase 3
Start date October 2005
Completion date November 2006

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