Efficacy and safety of low-dose atorvastatin plus ezetimibe for primary hypercholesterolemia: A randomized, double-blind, multicenter phase 3 trial
- Author(s)
- Tae Oh Kim; Kyounghoon Lee; Jin-Man Cho; Hyuck-Jun Yoon; Tae-Ho Park; Jung Hyun Choi; Jung-Won Suh; Seok-Yeon Kim; Hong-Seok Lim; Jong-Seon Park; Deok-Kyu Cho; Gyung-Min Park; Sung-Gyun Ahn; Sanghoon Shin; Sung Uk Kwon; Dae-Hyeok Kim; Sang-Rok Lee; Jung-Hoon Sung; Hwan-Cheol Park; Seung-Whan Lee
- Keimyung Author(s)
- Yoon, Hyuck Jun
- Department
- Dept. of Internal Medicine (내과학)
- Journal Title
- Lipids
- Issued Date
- 2025
- Volume
- 60
- Issue
- 5
- Abstract
- Studies have suggested that low-dose statin monotherapy may be insufficient for target LDL-C levels. In this randomized, double-blind, multicenter phase 3 trial, we evaluated the efficacy of combined ezetimibe and low-dose atorvastatin in 222 Korean patients with primary hypercholesterolemia. Participants received either 10-mg ezetimibe/5-mg atorvastatin (EZE10/ATV5), 10-mg ezetimibe (EZE10), 5-mg atorvastatin (ATV5), or 10-mg atorvastatin (ATV10). At 8 weeks, EZE10/ATV5 achieved the greatest LDL-C reduction (−44.8%) compared with EZE10 (−12.7%, p < 0.0001), ATV5 (−27.3%, p < 0.0001), and ATV10 (−32.0%, p = 0.0012). The combination therapy showed the highest LDL-C goal achievement rate (41.1% vs. EZE10 8.9%, p < 0.0001; ATV5 10.9%, p < 0.0001; ATV10 27.3%, p = 0.0342), particularly in moderate to high-risk patients. Additionally, EZE10/ATV5 had the lowest adverse events among all groups (6.9% vs. 15.0%, 12.3%, and 27.6%, p = 0.017), with most events being mild. These findings suggest that the combination of ezetimibe and low-dose atorvastatin provides superior lipid-lowering efficacy with an improved safety profile, offering an effective treatment for primary hypercholesterolemia in Korean patients.
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