Trials / Completed
CompletedNCT00654225
Treatment of Hypercholesterolaemia in South Asian Subjects (IRIS)
A 6-Week, Randomized,Open-Label, Comparative Study to Evaluate the Efficacy and Safety of Rosuvastatin and Atorvastatin in the Treatment of Hypercholesterolaemia in South Asian Subjects.
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 2,340 (estimated)
- Sponsor
- AstraZeneca · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to compare the effect of 6 weeks of treatment with Rosuvastatin with 6 weeks of treatment with Atorvastatin in South Asian subjects with hypercholesterolemia.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Rosuvastatin | |
| DRUG | Atorvastatin |
Timeline
- Start date
- 2002-10-01
- Completion
- 2005-03-01
- First posted
- 2008-04-07
- Last updated
- 2009-03-16
Source: ClinicalTrials.gov record NCT00654225. Inclusion in this directory is not an endorsement.