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法规知识库 · EMA 集中审评

Imatinib medac

imatinib · EMEA/H/C/002692 · 已撤市

仿制药

获批上市许可

2013-09-25

欧委会决定日

2018-04-11

持有人 / 申请人

Medac

终止日期字段

2019-02-14

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:L01XE01

治疗领域:Precursor Cell Lymphoblastic Leukemia-Lymphoma;Dermatofibrosarcoma;Leukemia, Myelogenous, Chronic, BCR-ABL Positive;Myelodysplastic-Myeloproliferative Diseases;Hypereosinophilic Syndrome

药理分类:Protein kinase inhibitors

修订号:5 · 最新影响 PI 的程序:IB/0009

适应症(原文):Imatinib medac is indicated for the treatment of: paediatric patients with newly diagnosed Philadelphia chromosome (bcr-abl) positive (Ph+) chronic myeloid leukaemia (CML) for whom bone marrow transplantation is not considered as the first line of treatment; paediatric patients with Ph+CML in chronic phase after failure of interferon-alpha therapy, or in accelerated phase; adult and paediatric patients with Ph+CML in blast crisis; adult and paediatric patients with newly diagnosed Philadelphia chromosome positive acute lymphoblastic leukaemia (Ph+ALL) integrated with chemotherapy; adult patients with relapsed or refractory Ph+ALL as monotherapy; adult patients with myelodysplastic/myeloproliferative diseases (MDS/MPD) associated with platelet-derived growth factor receptor (PDGFR) gene re-arrangements; adult patients with advanced hypereosinophilic syndrome (HES) and/or chronic eosinophilic leukaemia (CEL) with FIP1L1-PDGFR? rearrangement; adult patients with unresectable dermatofibrosarcoma protuberans (DFSP) and adult patients with recurrent and/or metastatic DFSP who are not eligible for surgery. The effect of imatinib on the outcome of bone marrow transplantation has not been determined. In adult and paediatric patients, the effectiveness of imatinib is based on overall haematological and cytogenetic response rates and progression-free survival in CML, on haematological and cytogenetic response rates in Ph+ALL, MDS/MPD, on haematological response rates in HES/CEL and on objective response rates in adult patients with unresectable and/or metastatic DFSP. The experience with imatinib in patients with MDS/MPD associated with PDGFR gene re-arrangements is very limited. Except in newly diagnosed chronic phase CML, there are no controlled trials demonstrating a clinical benefit or increased survival for these diseases.

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. 2019-02-14 · 上市许可终止(撤市/失效/撤销等)

    Withdrawn

  2. 2018-04-11 · 欧委会决定

  3. 2013-09-25 · 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 3产品信息 2其他 0

EPAR / 审评资料

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

    procedural-steps-after · 2018-05-14

    打开官方文件 ↗
  • Imatinib medac : EPAR - Summary for the public

    overview · 2015-06-26 · EMA/268384/2015

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

    assessment-report · 2013-10-23 · EMA/622006/2013

    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。