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

Outcome

Met primary endpoint

paper the RE10/10 group had a greater reduction in LDL-C level compared to the R20 group (-22.9±2.6% vs. -15.6 ± 2.5% [p=0.041] PMID 37800112 ↗

Drugs

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