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法规知识库 · EMA 集中审评

Herceptin

trastuzumab · EMEA/H/C/000278 · 已授权

获批上市许可

2000-08-28

欧委会决定日

2026-10-29

持有人 / 申请人

Roche Registration GmbH

终止日期字段

无

从产品到官方文件

文件记录

18

官方索引 18

EPAR / 审评

15

assessment / overview 等

产品信息

3

PI / presentations

其他

0

RMP / PIP 等

ATC:L01FD01

治疗领域:Stomach Neoplasms;Breast Neoplasms

药理分类:Antineoplastic agents

修订号:48 · 最新影响 PI 的程序:VR/0000362557

适应症(原文):Breast cancer Metastatic breast cancer Herceptin is indicated for the treatment of patients with HER2-positive metastatic breast cancer: as monotherapy for the treatment of those patients who have received at least two chemotherapy regimens for their metastatic disease. Prior chemotherapy must have included at least an anthracycline and a taxane unless patients are unsuitable for these treatments. Hormone-receptor-positive patients must also have failed hormonal therapy, unless patients are unsuitable for these treatments; in combination with paclitaxel for the treatment of those patients who have not received chemotherapy for their metastatic disease and for whom an anthracycline is not suitable; in combination with docetaxel for the treatment of those patients who have not received chemotherapy for their metastatic disease; in combination with an aromatase inhibitor for the treatment of postmenopausal patients with hormone-receptor-positive metastatic breast cancer, not previously treated with trastuzumab. Early breast cancer Herceptin is indicated for the treatment of patients with HER2-positive early breast cancer: following surgery, chemotherapy (neoadjuvant or adjuvant) and radiotherapy (if applicable); following adjuvant chemotherapy with doxorubicin and cyclophosphamide, in combination with paclitaxel or docetaxel; in combination with adjuvant chemotherapy consisting of docetaxel and carboplatin; in combination with neoadjuvant chemotherapy followed by adjuvant Herceptin therapy, for locally advanced (including inflammatory) disease or tumours >2 cm in diameter. Herceptin should only be used in patients with metastatic or early breast cancer whose tumours have either HER2 overexpression or HER2 gene amplification as determined by an accurate and validated assay. Metastatic gastric cancer Herceptin in combination with capecitabine or 5-fluorouracil and cisplatin is indicated for the treatment of patients with HER2-positive metastatic adenocarcinoma of the stomach or gastroesophageal junction who have not received prior anticancer treatment for their metastatic disease. Herceptin should only be used in patients with metastatic gastric cancer whose tumours have HER2 overexpression as defined by IHC2+ and a confirmatory SISH or FISH result, or by an IHC3+ result. Accurate and validated assay methods should be used.

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. 2026-10-29 · 欧委会决定

  2. 2000-08-28 · 获批上市许可

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 15产品信息 3其他 0

EPAR / 审评资料

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

    procedural-steps-after · 2026-11-09

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  • Herceptin : EPAR - Risk management plan

    rmp · 2026-03-02

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

    procedural-steps-after · 2024-08-20

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  • Herceptin : EPAR - Risk management plan summary

    rmp-summary · 2021-09-10

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  • Herceptin-H-C-PSUSA-00003010-201809 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation

    scientific-conclusion · 2019-10-09 · EMA/429226/2019

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  • Herceptin-H-C-278-X-0060 : EPAR - Assessment Report - Extension

    variation-report · 2013-12-11 · EMA/CHMP/751770/2012 Corr 1

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  • Herceptin : EPAR - Summary for the public

    overview · 2013-10-25

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  • Herceptin-H-C-278-II-0057 : EPAR - Assessment Report - Variation

    variation-report · 2012-05-07 · EMA/36190/2012

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  • Herceptin-H-C-278-II-0053 : EPAR - Assessment Report - Variation

    variation-report · 2011-05-19 · EMA/234266/2011

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  • Herceptin-H-C-278-II-0047 : EPAR - Assessment Report - Variation

    variation-report · 2010-03-01

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  • Herceptin-H-C-278-II-0033 : EPAR - Scientific Discussion - Variation

    scientific-discussion-variation · 2007-08-08

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  • Herceptin-H-C-278-II-0026 : EPAR - Scientific Discussion - Variation

    scientific-discussion-variation · 2006-06-09

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  • Herceptin : EPAR - Procedural steps taken before authorisation

    procedural-steps-before · 2005-10-21

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  • Herceptin : EPAR - Scientific Discussion

    scientific-discussion · 2005-10-21

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  • Herceptin : EPAR - Steps taken after authorisation when a cutoff date has been used

    steps-after-cutoff · 2005-10-21

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产品信息

  • Herceptin : EPAR - Product information - tracked changes

    product-information-tracked-changes · 2026-11-09

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  • Herceptin : EPAR - Product Information

    product-information · 2026-11-09

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  • Herceptin : EPAR - All Authorised presentations

    all-authorised-presentations · 2017-04-19

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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。