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法规知识库 · EMA 集中审评

Enhertu

trastuzumab deruxtecan · EMEA/H/C/005124 · 已授权

附条件批准额外监测

获批上市许可

2021-01-18

欧委会决定日

2026-10-20

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

15

官方索引 15

EPAR / 审评

12

assessment / overview 等

产品信息

3

PI / presentations

其他

0

RMP / PIP 等

ATC:L01FD04

治疗领域:Breast Neoplasms

药理分类:Antineoplastic agents

修订号:23 · 最新影响 PI 的程序:EMA/VR/0000377808

适应症(原文):Breast cancerHER2-positive breast cancerEnhertu as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic HER2-positive breast cancer who have received one or more prior anti-HER2-based regimens.HER2-low and HER2-ultralow breast cancerEnhertu as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic hormone receptor (HR)-positive, HER2-low or HER2-ultralow breast cancer who have received at least one endocrine therapy in the metastatic setting and who are not considered suitable for endocrine therapy as the next line of treatment (see sections 4.2 and 5.1). HER2-low breast cancer who have received prior chemotherapy in the metastatic setting or developed disease recurrence during or within 6 months of completing adjuvant chemotherapy (see section 4.2). Non-small cell lung cancer (NSCLC)Enhertu as monotherapy is indicated for the treatment of adult patients with advanced NSCLC whose tumours have an activating HER2 (ERBB2) mutation and who require systemic therapy following platinum-based chemotherapy with or without immunotherapy.Gastric cancer Enhertu as monotherapy is indicated for the treatment of adult patients with advanced HER2-positive gastric or gastroesophageal junction (GEJ) adenocarcinoma who have received a prior trastuzumab-based regimen. Other unresectable or metastatic solid tumours Enhertu as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic HER2-positive (IHC3+) solid tumours who have received prior treatment and who have no satisfactory treatment options (see sections 4.4 and 5.1; for biomarker-based patient selection, see section 4.2).

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. 2026-10-20 · 欧委会决定

  2. 2021-01-18 · 获批上市许可

  3. 2020-12-10 · 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 12产品信息 3其他 0

EPAR / 审评资料

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

    procedural-steps-after · 2026-10-20

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  • Enhertu : EPAR - Risk management plan

    rmp · 2026-10-20

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  • Enhertu-VR-0000293327 : EPAR - Assessment report - Variation

    variation-report · 2026-07-17 · EMADOC-1700519818-3246710

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  • Enhertu : EPAR - Medicine overview

    overview · 2026-07-17 · EMADOC-1829012207-55055

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  • Enhertu-H-C-005124-II-0027 : EPAR - Assessment report

    variation-report · 2026-04-07 · EMA/444980/2023

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  • Enhertu-H-C-005124-II-0022 : EPAR - Assessment Report - Variation

    variation-report · 2026-04-07 · EMA/CHMP/14752/2023

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

    procedural-steps-after · 2025-12-03

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  • Enhertu-H-C-005124-II-0048 : EPAR - Assessment report - Variation

    variation-report · 2025-04-28 · EMA/109425/2025

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  • Enhertu-H-C-PSUSA-00010894-202406 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation

    scientific-conclusion · 2025-03-31 · EMA/21594/2025

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  • Enhertu-H-C-005124-II-0012 : EPAR - Assessment Report - Variation

    variation-report · 2023-02-16 · EMA/CHMP/931431/2022

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  • Enhertu-H-C-005124-II-0014 : EPAR - Assessment Report - Variation

    variation-report · 2022-08-02 · EMA/CHMP/636117/2022

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  • Enhertu : EPAR - Public assessment report

    assessment-report · 2021-02-08 · EMA/CHMP/636117/2022

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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。