Cited by 114Lipoproteins and Cardiovascular HealthLipid metabolism and disordersCholesterol and Lipid Metabolism

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

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Kiyosue, Arihiro, Honarpour, Narimon, Kurtz, Christopher, Xue, Allen, Wasserman, Scott M., Hirayama, Atsushi·2016·The American Journal of Cardiology

Abstract

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/dl. Adverse events and laboratory values were recorded. Four hundred four patients were randomized to study drug. At baseline, the mean (SD) 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.

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References 28 · Cited by 114

Research works printed but not linked: 1

  1. TESLA Part B): a randomised, double-blind, placebo-controlled trial. Lancet 2015;385:341e350.

Authors
Kiyosue, A., Honarpour, N., Kurtz, C., Xue, A., Wasserman, S. M., & Hirayama, A.
Affiliations
  • The University of Tokyo (JP)
  • Amgen (United States) (US)
  • Nihon University (JP)
Corresponding author
Kiyosue, Arihiro
Venue
The American Journal of Cardiology
Publisher
Elsevier BV
Published
2016-01
Volume
117
Issue
1
Pages
40-47
ISSN
0002-9149 (ISSN-L)
OpenAlex
W1751918875
Cited by
114
References
28
Citations by year
2026: 2 · 2025: 12 · 2024: 8 · 2023: 9 · 2022: 7 · 2021: 6 · 2020: 13 · 2019: 13 · 2018: 10 · 2017: 27 · 2016: 7
FWCI
14.77
Type
journal article
Language
en
Open access
Locations
  • The American Journal of Cardiology (publishedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Surgery › Lipoproteins and Cardiovascular Health
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Lipid metabolism and disorders
  • Health Sciences › Medicine › Surgery › Cholesterol and Lipid Metabolism
Keywords
evolocumab, PCSK9 inhibition, atorvastatin, LDL cholesterol lowering, hyperlipidemia, mixed dyslipidemia, high cardiovascular risk, Japanese patients, monoclonal antibodies, statin therapy, dosing regimen, lipid-lowering therapy, adverse events
MeSH terms
Adult, Aged, Aged, 80 and over, Antibodies, Monoclonal, Cardiovascular Diseases, Double-Blind Method, Drug Administration Schedule, Drug Therapy, Combination, Female, Humans, Hyperlipidemias, Injections, Subcutaneous, Japan, Lipids, Male, Middle Aged, Morbidity, Risk Factors, Risk Assessment, Hydroxymethylglutaryl-CoA Reductase Inhibitors, Young Adult, Antibodies, Monoclonal, Humanized

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