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
| Type | Name | Description |
|---|---|---|
| DRUG | Pitavastatin | 2 mg QD |
| DRUG | Atorvastatin | 10 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.