Efficacy and safety of low-dose atorvastatin plus ezetimibe for primary hypercholesterolemia: A randomized, double-blind, multicenter phase 3 trialopen access
- Authors
- Kim, Tae Oh; Lee, Kyounghoon; Cho, Jin-Man; Yoon, Hyuck-Jun; Park, Tae-Ho; Choi, Jung Hyun; Suh, Jung-Won; Park, Hwan-Cheol; Kim, Seok-Yeon; Lim, Hong-Seok; Park, Jong-Seon; Cho, Deok-Kyu; Park, Gyung-Min; Ahn, Sung-Gyun; Shin, Sanghoon; Kwon, Sung Uk; Kim, Dae-Hyeok; Lee, Sang-Rok; Sung, Jung-Hoon; Lee, Seung-Whan
- Issue Date
- Sep-2025
- Publisher
- WILEY
- Keywords
- atorvastatin; clinical trial; ezetimibe; hypercholesterolemia; LDL; lipoprotein; phase III
- Citation
- LIPIDS, v.60, no.5, pp 317 - 326
- Pages
- 10
- Indexed
- SCIE
SCOPUS
- Journal Title
- LIPIDS
- Volume
- 60
- Number
- 5
- Start Page
- 317
- End Page
- 326
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/212807
- DOI
- 10.1002/lipd.12442
- ISSN
- 0024-4201
1558-9307
- 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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