法规知识库 · EMA 集中审评
Nustendi
bempedoic acid;ezetimibe · EMEA/H/C/004959 · 已授权
获批上市许可
2020-03-27
欧委会决定日
2026-01-15
持有人 / 申请人
Daiichi Sankyo Europe GmbH
终止日期字段
无
从产品到官方文件
文件记录
8
官方索引 8
EPAR / 审评
6
assessment / overview 等
产品信息
2
PI / presentations
其他
0
RMP / PIP 等
ATC:C10B
治疗领域:Hypercholesterolemia;Dyslipidemias
药理分类:Lipid modifying agents
修订号:9 · 最新影响 PI 的程序:EMA/VR/0000286873
适应症(原文):Hypercholesterolaemia and mixed dyslipidaemiaNustendi is indicated in adults with primary hypercholesterolaemia (heterozygous familial and non-familial) or mixed dyslipidaemia, as an adjunct to diet:• in combination with a statin in patients unable to reach LDL-C goals with the maximum tolerated dose of a statin in addition to ezetimibe • alone in patients who are either statin-intolerant or for whom a statin is contraindicated, and are unable to reach LDL-C goals with ezetimibe alone,• in patients already being treated with the combination of bempedoic acid and ezetimibe as separate tablets with or without statinCardiovascular diseaseNustendi is indicated in adults with established or at high risk for atherosclerotic cardiovascular disease to reduce cardiovascular risk by lowering LDL-C levels, as an adjunct to correction of other risk factors:• in patients on a maximum tolerated dose of a statin and not adequately controlled with additional ezetimibe treatment or,• in patients who are either statin-intolerant, or for whom a statin is contraindicated, and not adequately controlled with ezetimibe treatment or, • in patients already being treated with the combination of bempedoic acid and ezetimibe as separate tablets.For study results with respect to effects on LDL-C, cardiovascular events and populations studied see section 5.1.
关键日期时间轴
来自 EMA medicines JSON 日期字段;缺失字段不展示,不补推结论。
2026-01-15 · 欧委会决定
2020-03-27 · 获批上市许可
2020-01-30 · CHMP 意见通过
说明书、EPAR 与其他文件
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EPAR / 审评资料
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Nustendi : EPAR - Procedural steps taken and scientific information after authorisation
procedural-steps-after · 2026-02-27
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Nustendi : EPAR - Procedural steps taken and scientific information after authorisation (archive)
procedural-steps-after · 2026-02-27
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Nustendi : EPAR - Risk management plan
rmp · 2026-02-27
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Nustendi : EPAR - Medicine overview
overview · 2025-06-23
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Nustendi-H-C-004959-II-0035 : EPAR - Assessment report - Variation
variation-report · 2024-06-20 · EMA/287504/2024
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Nustendi : EPAR - Public assessment report
assessment-report · 2020-04-24 · EMA/CHMP/86205/2020
数据来自 EMA 官方 JSON;最终以 EMA / 欧委会文件为准。本页不自动给出安全或非安全结论。