drugset / Trial / NCT03494270

High-intensity Rosuvastatin and Moderate-intensity Rosuvastatin/Ezetimibe in ASCVD Patients

NCT03494270

Phase 4 Completed 270 enrolled Yuhan Corporation
RandomizedParallel-groupOpen-labelTreatment

Summary

This study will evaluate the efficacy and safety of high-intensity rosuvastatin and moderate-intensity rosuvastatin/ezetimibe in ASCVD patients.

Timeline

Start
2018-03-18
Primary completion
2019-09-26
Completion
2019-09-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Ezetimibe Unknown 10 mg
Subject Rosuvastatin Small molecule 10 mg
Subject Rosuvastatin Small molecule 20 mg