法规知识库 · EMA 集中审评
Mvasi
bevacizumab · EMEA/H/C/004728 · 已授权
获批上市许可
2018-01-15
欧委会决定日
2026-08-28
持有人 / 申请人
Amgen Europe B.V.
终止日期字段
无
从产品到官方文件
文件记录
10
官方索引 10
EPAR / 审评
7
assessment / overview 等
产品信息
3
PI / presentations
其他
0
RMP / PIP 等
ATC:L01XC07
治疗领域:Carcinoma, Renal Cell;Peritoneal Neoplasms;Ovarian Neoplasms;Breast Neoplasms;Carcinoma, Non-Small-Cell Lung;Fallopian Tube Neoplasms
药理分类:Antineoplastic agents
修订号:19 · 最新影响 PI 的程序:T/0000363266
适应症(原文):Mvasi in combination with fluoropyrimidine-based chemotherapy is indicated for treatment of adult patients with metastatic carcinoma of the colon or rectum. Mvasi in combination with paclitaxel is indicated for first-line treatment of adult patients with metastatic breast cancer. For further information as to human epidermal growth factor receptor 2 (HER2) status, please refer to section 5.1. Mvasi, in addition to platinum-based chemotherapy, is indicated for first-line treatment of adult patients with unresectable advanced, metastatic or recurrent non-small cell lung cancer other than predominantly squamous cell histology. Mvasi in combination with interferon alfa-2a is indicated for first-line treatment of adult patients with advanced and/or metastatic renal cell cancer. Mvasi, in combination with carboplatin and paclitaxel is indicated for the front-line treatment of adult patients with advanced (International Federation of Gynecology and Obstetrics (FIGO) stages IIIB, IIIC and IV) epithelial ovarian, fallopian tube, or primary peritoneal cancer. Mvasi, in combination with carboplatin and gemcitabine or in combination with carboplatin and paclitaxel, is indicated for treatment of adult patients with first recurrence of platinum-sensitive epithelial ovarian, fallopian tube or primary peritoneal cancer who have not received prior therapy with bevacizumab or other VEGF inhibitors or VEGF receptor-targeted agents. Mvasi in combination with paclitaxel, topotecan, or pegylated liposomal doxorubicin is indicated for the treatment of adult patients with platinum-resistant recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer who received no more than two prior chemotherapy regimens and who have not received prior therapy with bevacizumab or other VEGF inhibitors or VEGF receptor-targeted agents. Mvasi, in combination with paclitaxel and cisplatin or, alternatively, paclitaxel and topotecan in patients who cannot receive platinum therapy, is indicated for the treatment of adult patients with persistent, recurrent, or metastatic carcinoma of the cervix.
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。
2026-08-28 · 欧委会决定
2018-01-15 · 获批上市许可
2017-11-08 · 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
- 打开官方文件 ↗
Mvasi : EPAR - Procedural steps taken and scientific information after authorisation
procedural-steps-after · 2026-10-08
- 打开官方文件 ↗
Mvasi-PSUSA-00000403-202502 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation
scientific-conclusion · 2026-01-27 · EMADOC-1700519818-2470418
- 打开官方文件 ↗
Mvasi : EPAR - Procedural steps taken and scientific information after authorisation (archive)
procedural-steps-after · 2026-01-27
- 打开官方文件 ↗
Mvasi-H-C-PSUSA-00000403-202202 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation
scientific-conclusion · 2023-01-05 · EMA/921971/2022
- 打开官方文件 ↗
Mvasi : EPAR - Risk-management-plan summary
rmp-summary · 2021-05-21
- 打开官方文件 ↗
Mvasi : EPAR - Medicine overview
overview · 2020-04-30 · EMA/3108/2020
- 打开官方文件 ↗
Mvasi : EPAR - Public assessment report
assessment-report · 2018-01-31 · EMA/798844/2017
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。