A Phase 3 Study of Evolocumab (AMG 145) in Statin-Treated Japanese Patients at High Cardiovascular Risk
Open accessAbstract
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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In PQRST, suppressive effects on atherosclerosis progression in the femoral arteries could not be achieved with probucol administration in addition to diet therapy and cholestyramine treatment.
“In PQRST, however, suppressive effects on atherosclerosis progression in the femoral arteries could not be achieved with probucol administration in addition to diet therapy and cholestyramine treatment680).”
From Japan Atherosclerosis Society (JAS) guidelines for prevention of atherosclerotic cardiovascular diseases 2017 (2018) · cites this paper as [680]
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References 28 · Cited by 114
Research works printed but not linked: 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
- hybrid
- doi.org
- Licence
- 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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