A Phase 3 Study of Evolocumab (AMG 145) in Statin-Treated Japanese Patients at High Cardiovascular Risk

被引:102
作者
Kiyosue, Arihiro [1 ,2 ]
Honarpour, Narimon [3 ]
Kurtz, Christopher [3 ]
Xue, Allen [3 ]
Wasserman, Scott M. [3 ]
Hirayama, Atsushi [4 ]
机构
[1] Univ Tokyo, Grad Sch Med, Dept Cardiovasc Med, Tokyo, Japan
[2] Tokyo Eki Ctr Bldg Clin, Tokyo, Japan
[3] Amgen Inc, Thousand Oaks, CA 91320 USA
[4] Nihon Univ, Sch Med, Dept Med, Div Cardiovasc Med, Tokyo, Japan
关键词
SUBTILISIN/KEXIN TYPE 9; HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA; LIPOPROTEIN CHOLESTEROL LEVELS; CORONARY-HEART-DISEASE; MONOCLONAL-ANTIBODY; DOUBLE-BLIND; PCSK9; INHIBITION; REDUCING LIPIDS; LDL-C; EFFICACY;
D O I
10.1016/j.amjcard.2015.10.021
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Evolocumab (AMG 145), a fully human monoclonal antibody against PCSK9, significantly reduced low-density lipoprotein cholesterol (LDL-C) levels in phase 2 and 3 studies. This phase 3 study evaluated the efficacy and safety of evolocumab plus atorvastatin in Japanese patients with hyperlipidemia or mixed dyslipidemia and high cardiovascular risk. Patients were randomized to atorvastatin 5 or 20 mg/day for 4 weeks. Subsequently, patients underwent second randomization to evolocumab 140 mg biweekly (Q2W) or 420 mg monthly (QM) or placebo Q2W or QM. Coprimary end points were % change from baseline in LDL-C at week 12 and mean of weeks 10 and 12. Secondary end points included change and % change in other lipids and proportion of patients reaching LDL-C < 70 mg/d1. Adverse events and laboratory values were recorded. Four hundred four patients were randomized to study drug. At baseline, the mean (SP) age was 61 (10) years (placebo) and 62 (11) years (evolocumab); 39% and 40% were women; 14% and 12% had cerebrovascular or peripheral arterial disease; and 51% and 47% had diabetes. At entry, mean (SD) calculated LDL-C was 128 (23) mg/dL; after stabilization on atorvastatin 5 and 20 mg/day, baseline LDL-C levels were 118 (35) and 94 (24) mg/dL, respectively. Mean LDL-C reductions at week 12 for evolocumab versus placebo ranged from 67% to 76%. No imbalances were observed in adverse events between treatment groups. Efficacy and safety for Q2W or QM evolocumab dosing were similar. In conclusion, in high-risk Japanese patients receiving stable statin therapy, evolocumab markedly reduced LDL-C and was well tolerated. (c) 2016 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:40 / 47
页数:8
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