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Study to Compare the Efficacy and Safety of Pitavastatin and Simvastatin

NCT00309777 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 857

Last updated 2010-01-12

Study results available
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Summary

The purpose of this study is to compare the efficacy and safety of pitavastatin with that of simvastatin.

Conditions

Interventions

DRUG

Pitavastatin

Pitavastatin once daily

DRUG

Simvastatin

Simvastatin once daily

Sponsors & Collaborators

  • Kowa Research Europe

    lead INDUSTRY

Principal Investigators

  • Dragos Budinski, Med Dr. · Medical Director

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-09-30
Primary Completion
2006-10-31
Completion
2006-10-31

Countries

  • Finland
  • Italy
  • Norway
  • Russia
  • United Kingdom

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00309777 on ClinicalTrials.gov