Clinical Trials Directory

Trials / Unknown

UnknownNCT01386853

Efficacy and Safety Study of Pitavastatin and Atorvastatin in High Risk Hypercholesterolemic Patients

A 12-week, Randomized, Multicenter, Double-blind, Active-controlled, Non-inferiority Study to Compare the Efficacy and Safety of Pitavastatin and Atorvastatin in High Risk Hypercholesterolemic Patients

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
200 (estimated)
Sponsor
Tai Tien Pharmaceuticals Co., Ltd. · Industry
Sex
All
Age
20 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This is a 12-week, randomized, multicenter, double-blind, active-controlled, non-inferiority study (TATPITA20101005) to compare the efficacy and safety of pitavastatin (Livalo®) and atorvastatin (Lipitor®) in high risk hypercholesterolemic patients.

Conditions

Interventions

TypeNameDescription
DRUGPitavastatin2 mg QD
DRUGAtorvastatin10 mg QD

Timeline

Start date
2011-07-01
Primary completion
2012-03-01
Completion
2012-07-01
First posted
2011-07-01
Last updated
2011-07-01

Locations

6 sites across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT01386853. Inclusion in this directory is not an endorsement.