drugset / Trial / NCT00396240

ORBITAL: Open-Label Primary Care Study: Rosuvastatin Based Compliance Initiatives Linked To Achievement Of LDL Goals

NCT00396240 ↗

Phase 4 Withdrawn 1294 enrolled AstraZeneca
RandomizedParallel-groupOpen-labelTreatment

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.

Timeline

Start
2002-02
Primary completion
—
Completion
—

Outcome

Outcome not reported

Stopped: “study cancelled prior to FSI”

Drugs

EvaluationDrugModalityDoseRoute
Subject Rosuvastatin Small molecule 20 mg —

Indications