医学
家族性高胆固醇血症
PCSK9
内科学
以兹提米比
内分泌学
他汀类
Evolocumab公司
可欣
安慰剂
阿利罗库单抗
胃肠病学
复合杂合度
脂蛋白
胆固醇
低密度脂蛋白受体
生物化学
化学
突变
病理
替代医学
载脂蛋白A1
基因
作者
Frederick J. Raal,Robert C. Scott,Ransi Somaratne,Ian Bridges,Gang Li,Scott M. Wasserman,Evan A. Stein
出处
期刊:Circulation
[Lippincott Williams & Wilkins]
日期:2012-11-06
卷期号:126 (20): 2408-2417
被引量:499
标识
DOI:10.1161/circulationaha.112.144055
摘要
Background— Despite statin treatment, many patients with heterozygous familial hypercholesterolemia do not reach desired low-density lipoprotein cholesterol (LDL-C) targets. AMG 145, a fully human monoclonal antibody against proprotein convertase subtilisin/kexin type 9 (PCSK9) serine protease, demonstrated significant reductions in LDL-C in phase 1 studies. This phase 2, multicenter, double-blind, randomized, placebo-controlled, dose-ranging study evaluated the efficacy and safety of AMG 145 in heterozygous familial hypercholesterolemia patients. Methods and Results— Patients with heterozygous familial hypercholesterolemia diagnosed by Simon Broome criteria with LDL-C ≥2.6 mmol/L (100 mg/dL) despite statin therapy with or without ezetimibe were randomized 1:1:1 to AMG 145 350 mg, AMG 145 420 mg, or placebo-administered subcutaneously every 4 weeks. The primary end point was percentage change from baseline in LDL-C at week 12. Of 168 patients randomized, 167 received investigational product and were included in the full analysis set (mean [SD] age, 50 [13] years; 47% female; 89% white; mean [SD] baseline LDL-C, 4.0 [1.1] mmol/L (156 [42] mg/dL)). At week 12, LDL-C reduction measured by preparative ultracentrifugation (least squares mean [standard error (SE)]) was 43 (3)% and 55 (3)% with AMG 145 350 mg and 420 mg, respectively, compared with 1 (3)% increase with placebo ( P <0.001 for both dose groups). Serious adverse events (not considered treatment-related) occurred in 2 patients on AMG 145. Conclusions— AMG 145 administered every 4 weeks yielded rapid and substantial reductions in LDL-C in heterozygous familial hypercholesterolemia patients despite intensive statin use, with or without ezetimibe, with minimal adverse events and good tolerability. Clinical Trial Registration— URL: http://www.clinicaltrials.gov . Unique identifier: NCT01375751.
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