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Clinical Trial Summary

24 week open label study to compare the treatment either with rosuvastatin or rosuvastatin plus initiatives to improve compliance. If the subject does not reach the EAS LDL-C treatment goal at week 12, rosuvastatin will be titrated from 10mg to 20mg.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00396240
Study type Interventional
Source AstraZeneca
Contact
Status Withdrawn
Phase Phase 4
Start date February 2002

See also
  Status Clinical Trial Phase
Completed NCT00269204 - Lipid Efficacy/Tolerability Study (0524A-020) Phase 3