跳到正文
  1. EMA · What's New

    EMA 授权 rilzabrutinib(Wayrilz)用于既往治疗无效的成人免疫性血小板减少症

    EMA 于 2025 年 12 月 22 日授予 Sanofi 的 rilzabrutinib(Wayrilz)欧盟上市授权,用于既往治疗无效的成人免疫性血小板减少症(ITP),并发布 Revision 1 的 EPAR。

    关注理由:EMA 发布 rilzabrutinib(Wayrilz)欧盟上市授权 EPAR,含 202 名成人 ITP 随机对照试验数据及 12 周无效停药规则,可用于孤儿药治疗路径跟踪。

  2. EMA · What's New

    EMA将多发性骨髓瘤药teclistamab(Tecvayli)的条件性上市许可转为标准许可(EPAR第11版)

    EMA更新teclistamab(Tecvayli)的EPAR:该药用于复发或难治性多发性骨髓瘤成人患者,2022年8月23日获欧盟条件性上市许可,2026年8月20日因公司提交额外数据转为标准上市许可。

    关注理由:该EPAR第11版记录teclistamab由条件性上市许可转为标准许可这一监管证据升级,并汇总其单药及联合daratumumab研究的疗效与安全性数据,便于跟踪多发性骨髓瘤后续监管动作。

  1. EMA · Withdrawn Applications

    临床试验:Withdrawn application: Truqap, 16/09/2026

    原文摘录:Truqap - withdrawal of application for variation to marketing authorisation Application withdrawn The application for a change to this medicine's authorisation has been withdrawn capivasertib Post-authorisation Human Overview AstraZeneca AB withdrew its a … News on Truqap Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 12-15 October 2026 16/10/2026 Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 22-25 April 2024 26/04/2024 More information on Truqap Truqap This page was last updated on 03/11/2026

    关注理由:这篇临床试验内容涉及随机对照研究,阅读重点可以放在研究分组、主要终点和随访结果上。

  1. EMA · Withdrawn Applications

    肿瘤学:Withdrawn application: Ibrance, 15/10/2026

    原文摘录:Ibrance - withdrawal of application for variation to marketing authorisation Application withdrawn The application for a change to this medicine's authorisation has been withdrawn palbociclib Post-authorisation Human Overview Pfizer Europe MA EEIG withdre … News on Ibrance Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 12-15 October 2026 16/10/2026 Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 12-15 September 2016 (corrected) 21/09/2016 New treatment for breast cancer 16/09/2016 More information on Ibrance Ibrance This page was last updated on 28/10/2026

    关注理由:这篇肿瘤学内容涉及临床试验,适合了解研究正在回答什么问题,试验阶段和主要终点需以原文为准。

  1. EMA · Withdrawn Applications

    儿科学:Withdrawn application: Kaftrio, 01/09/2026

    原文摘录:Kaftrio - withdrawal of application for variation to marketing authorisation Application withdrawn The application for a change to this medicine's authorisation has been withdrawn ivacaftor / tezacaftor / elexacaftor Post-authorisation Human Overview Vert … News on Kaftrio Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 14-17 September 2026 18/09/2026 Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 24-27 February 2025 28/02/2025 Combination of cystic fibrosis medicines to treat patients with rare mutations 28/02/2025 Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 11-14 September 2023 15/09/2023 Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 8-11 November 2021 12/11/2021 Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 22-25 March 2021 26/03/2021 Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 22-25 June 2020 26/06/2020 New medicine for cystic fibrosis patients 26/06/2020 More information on Kaftrio Kaftrio This page was last updated on 20/10/2026

    关注理由:如果关注儿科学,这条临床试验动态可用于了解研究设计,主要终点和试验阶段建议查看原文。

  1. WHO · Disease Outbreak News OData

    感染病学:Pneumonia of undetermined etiology - the Russian Federation

    原文摘录:Disease Outbreak News Pneumonia of undetermined etiology - Russian Federation 10 October 2026 See all DONs related to this event Situation at a glance On 2 October 2026, WHO became aware through media reports of the death of an employee of the Irkutsk Ant … item/2026-DON620 See all DONs related to this event

    关注理由:这条感染病学资料适合作为深入阅读入口,尤其要关注研究方法与结论是否匹配。

  1. EMA · Withdrawn Applications

    儿科学:Withdrawn application: Kalydeco, 01/09/2026

    原文摘录:Kalydeco - withdrawal of application for variation to marketing authorisation Application withdrawn The application for a change to this medicine's authorisation has been withdrawn ivacaftor Post-authorisation Human Overview Vertex Pharmaceuticals (Irelan … News on Kalydeco Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 14-17 September 2026 18/09/2026 Combination of cystic fibrosis medicines to treat patients with rare mutations 28/02/2025 Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 19-22 February 2024 23/02/2024 Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 11-14 September 2023 15/09/2023 Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 8-11 November 2021 12/11/2021 Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 22-25 March 2021 26/03/2021 Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 14-17 September 2020 18/09/2020 Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 20-23 July 2020 24/07/2020 Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 28-30 April 2020 30/04/2020 Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 14-17 October 2019 18/10/2019 Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 15-18 October 2018 19/10/2018 Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 23-26 July 2018 27/07/2018 Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 21-24 September 2015 25/09/2015 Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 23-26 June 2014 27/06/2014 More information on Kalydeco Kalydeco This page was last updated on 09/10/2026

    关注理由:这条儿科学临床试验动态值得跟踪,后续可结合原文核对试验进度、研究设计与结果披露情况。

已经到底了