法规知识库 · EMA 集中审评
Ritemvia
rituximab · EMEA/H/C/004725 · 已撤市
获批上市许可
2017-07-13
欧委会决定日
2020-10-09
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
5
官方索引 5
EPAR / 审评
3
assessment / overview 等
产品信息
2
PI / presentations
其他
0
RMP / PIP 等
ATC:L01XC02
治疗领域:Lymphoma, Non-Hodgkin;Microscopic Polyangiitis;Wegener Granulomatosis
药理分类:Antineoplastic agents
修订号:8 · 最新影响 PI 的程序:WS/1859/G
适应症(原文):Ritemvia is indicated in adults for the following indications: Non-Hodgkin’s lymphoma (NHL) Ritemvia is indicated for the treatment of previously untreated patients with stage III, IV follicular lymphoma in combination with chemotherapy. Ritemvia maintenance therapy is indicated for the treatment of follicular lymphoma patients responding to induction therapy. Ritemvia monotherapy is indicated for treatment of patients with stage III, IV follicular lymphoma who are chemo resistant or are in their second or subsequent relapse after chemotherapy. Ritemvia is indicated for the treatment of patients with CD20 positive diffuse large B cell non Hodgkin’s lymphoma in combination with CHOP (cyclophosphamide, doxorubicin, vincristine, prednisolone) chemotherapy. Granulomatosis with polyangiitis and microscopic polyangiitis. Ritemvia, in combination with glucocorticoids, is indicated for the induction of remission in adult patients with severe, active granulomatosis with polyangiitis (Wegener’s) (GPA) and microscopic polyangiitis (MPA).
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。
2020-10-09 · 欧委会决定
2017-07-13 · 获批上市许可
2017-05-18 · 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
- 打开官方文件 ↗
Ritemvia : EPAR - Procedural steps taken and scientific information after authorisation
procedural-steps-after · 2021-08-16
- 打开官方文件 ↗
Ritemvia : EPAR - Medicine overview
overview · 2021-08-16 · EMA/413555/2019
- 打开官方文件 ↗
Ritemvia : EPAR - Public assessment report
assessment-report · 2021-08-16 · EMA/CHMP/421799/2017
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。