跳到正文

法规知识库 · EMA 集中审评

Ogivri

trastuzumab · EMEA/H/C/004916 · 已授权

生物类似药

获批上市许可

2018-12-12

欧委会决定日

2026-02-20

持有人 / 申请人

Biosimilar Collaborations Ireland Limited

终止日期字段

无

从产品到官方文件

文件记录

7

官方索引 7

EPAR / 审评

5

assessment / overview 等

产品信息

2

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:13 · 最新影响 PI 的程序:N/0000326197

适应症(原文):Breast cancer Metastatic breast cancer Ogivri is indicated for the treatment of adult patients with HER2 positive metastatic breast cancer (MBC): 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 MBC, not previously treated with trastuzumab. Early breast cancer Ogivri is indicated for the treatment of adult patients with HER2 positive early breast cancer (EBC): 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 Ogivri therapy, for locally advanced (including inflammatory) disease or tumours > 2 cm in diameter. Ogivri should only be used in patients with metastatic or EBC whose tumours have either HER2 overexpression or HER2 gene amplification as determined by an accurate and validated assay. Metastatic gastric cancer Ogivri in combination with capecitabine or 5-fluorouracil and cisplatin is indicated for the treatment of adult patients with HER2 positive metastatic adenocarcinoma of the stomach or gastroesophageal junction who have not received prior anti-cancer treatment for their metastatic disease. Ogivri should only be used in patients with metastatic gastric cancer (MGC) whose tumours have HER2 overexpression as defined by IHC2+ and a confirmatory SISH or FISH result, or by an IHC 3+ 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. 2026-02-20 · 欧委会决定

  2. 2018-12-12 · 获批上市许可

  3. 2018-10-18 · 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 2其他 0

EPAR / 审评资料

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

    procedural-steps-after · 2026-02-23

    打开官方文件 ↗
  • Ogivri : EPAR - Procedural steps taken and scientific information after authorisation (archive)

    procedural-steps-after · 2026-02-23

    打开官方文件 ↗
  • Ogivri : EPAR - Medicine overview

    overview · 2019-01-09 · EMA/739554/2018

    打开官方文件 ↗
  • Ogivri : EPAR - Risk-management-plan summary

    rmp-summary · 2019-01-09

    打开官方文件 ↗
  • Ogivri : EPAR - Public assessment report

    assessment-report · 2019-01-09 · EMA/810499/2018

    打开官方文件 ↗

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。