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法规知识库 · EMA 集中审评

Omlyclo

omalizumab · EMEA/H/C/005958 · 已授权

生物类似药额外监测

获批上市许可

2024-05-16

欧委会决定日

2026-03-19

持有人 / 申请人

Celltrion Healthcare Hungary Kft.

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

5

assessment / overview 等

产品信息

3

PI / presentations

其他

0

RMP / PIP 等

ATC:R03DX05

治疗领域:Asthma;Urticaria

药理分类:Drugs for obstructive airway diseases

修订号:5 · 最新影响 PI 的程序:VR/0000315350

适应症(原文):Allergic asthma Omlyclo is indicated in adults, adolescents and children (6 to <12 years of age). Omlyclo treatment should only be considered for patients with convincing IgE (immunoglobulin E) mediated asthma (see section 4.2). Adults and adolescents (12 years of age and older) Omlyclo is indicated as add-on therapy to improve asthma control in patients with severe persistent allergic asthma who have a positive skin test or in vitro reactivity to a perennial aeroallergen and who have reduced lung function (FEV1 <80%) as well as frequent daytime symptoms or night-time awakenings and who have had multiple documented severe asthma exacerbations despite daily high-dose inhaled corticosteroids, plus a long-acting inhaled beta2-agonist. Children (6 to <12 years of age) Omlyclo is indicated as add-on therapy to improve asthma control in patients with severe persistent allergic asthma who have a positive skin test or in vitro reactivity to a perennial aeroallergen and frequent daytime symptoms or night-time awakenings and who have had multiple documented severe asthma exacerbations despite daily high-dose inhaled corticosteroids, plus a long-acting inhaled beta2-agonist. Chronic rhinosinusitis with nasal polyps (CRSwNP) Omlyclo is indicated as an add-on therapy with intranasal corticosteroids (INC) for the treatment of adults (18 years and above) with severe CRSwNP for whom therapy with INC does not provide adequate disease control. Chronic spontaneous urticaria (CSU) Omlyclo is indicated as add-on therapy for the treatment of chronic spontaneous urticaria in adult and adolescent (12 years and above) patients with inadequate response to H1 antihistamine treatment.

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。

  1. 2026-03-19 · 欧委会决定

  2. 2024-05-16 · 获批上市许可

  3. 2024-03-21 · CHMP 意见通过

说明书、EPAR 与其他文件

仅展示 EMA 官方 document_url;本站不下载或镜像 PDF。

EPAR / 审评资料 5产品信息 3其他 0

EPAR / 审评资料

  • Omlyclo : EPAR - Procedural steps taken and scientific information after authorisation

    procedural-steps-after · 2026-05-11

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  • Omlyclo : EPAR - Procedural steps taken and scientific information after authorisation (archive)

    procedural-steps-after · 2025-04-24

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  • Omlyclo : EPAR - Risk management plan

    rmp · 2025-04-24

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  • Omlyclo : EPAR - Medicine overview

    overview · 2024-06-03 · EMA/241111/2024

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  • Omlyclo : EPAR - Public assessment report

    assessment-report · 2024-05-29 · EMA/153515/2024

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产品信息

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。