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法规知识库 · EMA 集中审评

Noxafil

posaconazole · EMEA/H/C/000610 · 已授权

获批上市许可

2005-10-25

欧委会决定日

2026-03-05

持有人 / 申请人

Merck Sharp and Dohme B.V

终止日期字段

无

从产品到官方文件

文件记录

21

官方索引 21

EPAR / 审评

18

assessment / overview 等

产品信息

3

PI / presentations

其他

0

RMP / PIP 等

ATC:J02AC04

治疗领域:Candidiasis;Mycoses;Coccidioidomycosis;Aspergillosis

药理分类:Triazole and triazole derivatives

修订号:43 · 最新影响 PI 的程序:VR/0000263360

适应症(原文):Noxafil concentrate for solution for infusion is indicated for use in the treatment of the following invasive fungal infections in adult and paediatric patients from 2 years of age: Invasive aspergillosis Fusariosis in patients with disease that is refractory to amphotericin B or in patients who are intolerant of amphotericin B; Chromoblastomycosis and mycetoma in patients with disease that is refractory to itraconazole or in patients who are intolerant of itraconazole; Coccidioidomycosis in patients with disease that is refractory to amphotericin B, itraconazole or fluconazole or in patients who are intolerant of these medicinal products. Refractoriness is defined as progression of infection or failure to improve after a minimum of 7 days of prior therapeutic doses of effective antifungal therapy. Noxafil concentrate for solution for infusion is also indicated for prophylaxis of invasive fungal infections in adults and paediatric patients from 2 years of age: Patients receiving remission-induction chemotherapy for acute myelogenous leukaemia (AML) or myelodysplastic syndromes (MDS) expected to result in prolonged neutropenia and who are at high risk of developing invasive fungal infections; Hematopoietic stem cell transplant (HSCT) recipients who are undergoing high-dose immunosuppressive therapy for graft versus host disease (GVHD) and who are at high risk of developing invasive fungal infections. Please refer to the Summary of Product Characteristics of Noxafil oral suspension for use in adults with oropharyngeal candidiasis. Noxafil gastro-resistant tablets are indicated for use in the treatment of the following invasive fungal infections in adults and paediatric patients from 2 years of age weighing more than 40 kg: Invasive aspergillosis Fusariosis in patients with disease that is refractory to amphotericin B or in patients who are intolerant of amphotericin B; Chromoblastomycosis and mycetoma in patients with disease that is refractory to itraconazole or in patients who are intolerant of itraconazole; Coccidioidomycosis in patients with disease that is refractory to amphotericin B, itraconazole or fluconazole or in patients who are intolerant of these medicinal products. Refractoriness is defined as progression of infection or failure to improve after a minimum of 7 days of prior therapeutic doses of effective antifungal therapy. Noxafil gastro-resistant tablets are also indicated for prophylaxis of invasive fungal infections in adults and paediatric patients from 2 years of age weighing more than 40 kg: Patients receiving remission-induction chemotherapy for acute myelogenous leukaemia (AML) or myelodysplastic syndromes (MDS) expected to result in prolonged neutropenia and who are at high risk of developing invasive fungal infections; Hematopoietic stem cell transplant (HSCT) recipients who are undergoing high-dose immunosuppressive therapy for graft versus host disease and who are at high risk of developing invasive fungal infections. Please refer to the Summary of Product Characteristics of Noxafil oral suspension for use in oropharyngeal candidiasis. Noxafil oral suspension is indicated for use in the treatment of the following fungal infections in adults (see section 5.1): Invasive aspergillosis in patients with disease that is refractory to amphotericin B or itraconazole or in patients who are intolerant of these medicinal products; Fusariosis in patients with disease that is refractory to amphotericin B or in patients who are intolerant of amphotericin B; Chromoblastomycosis and mycetoma in patients with disease that is refractory to itraconazole or in patients who are intolerant of itraconazole; Coccidioidomycosis in patients with disease that is refractory to amphotericin B, itraconazole or fluconazole or in patients who are intolerant of these medicinal products; Oropharyngeal candidiasis: as first-line therapy in patients who have severe disease or are immunocompromised, in whom response to topical therapy is expected to be poor. Refractoriness is defined as progression of infection or failure to improve after a minimum of 7 days of prior therapeutic doses of effective antifungal therapy. Noxafil oral suspension is also indicated for prophylaxis of invasive fungal infections in the following patients: Patients receiving remission-induction chemotherapy for acute myelogenous leukaemia (AML) or myelodysplastic syndromes (MDS) expected to result in prolonged neutropenia and who are at high risk of developing invasive fungal infections; Hematopoietic stem cell transplant (HSCT) recipients who are undergoing high-dose immunosuppressive therapy for graft versus host disease and who are at high risk of developing invasive fungal infections. Please refer to the Summary of Product Characteristics of Noxafil concentrate for solution for infusion and the gastro-resistant tablets for use in primary treatment of invasive aspergillosis. Noxafil gastro resistant powder and solvent for oral suspension is indicated for use in the treatment of the following invasive fungal infections in paediatric patients from 2 years of age: Invasive aspergillosis Fusariosis in patients with disease that is refractory to amphotericin B or in patients who are intolerant of amphotericin B; Chromoblastomycosis and mycetoma in patients with disease that is refractory to itraconazole or in patients who are intolerant of itraconazole; Coccidioidomycosis in patients with disease that is refractory to amphotericin B, itraconazole or fluconazole or in patients who are intolerant of these medicinal products. Refractoriness is defined as progression of infection or failure to improve after a minimum of 7 days of prior therapeutic doses of effective antifungal therapy. Noxafil gastro-resistant powder and solvent for oral suspension is indicated for prophylaxis of invasive fungal infections in the following paediatric patients from 2 years of age: Patients receiving remission-induction chemotherapy for acute myelogenous leukaemia (AML) or myelodysplastic syndromes (MDS) expected to result in prolonged neutropenia and who are at high risk of developing invasive fungal infections; - Haematopoietic stem cell transplant (HSCT) recipients who are undergoing high-dose immunosuppressive therapy for graft versus host disease and who are at high risk of developing invasive fungal infections.

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. 2026-03-05 · 欧委会决定

  2. 2005-10-25 · 获批上市许可

  3. 2005-07-27 · 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 18产品信息 3其他 0

EPAR / 审评资料

  • Noxafil-VR-0000263360 : EPAR - Assessment report

    variation-report · 2026-03-24 · EMADOC-1700519818-2632882

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

    procedural-steps-after · 2026-03-24

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  • Noxafil : EPAR - Risk management plan

    rmp · 2026-03-24

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  • Noxafil : EPAR - Medicine overview

    overview · 2026-03-24 · EMA/709842/2021

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  • Noxafil : EPAR - Procedural steps taken and scientific information after authorisation (archive)

    procedural-steps-after · 2025-04-23

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  • Noxafil-H-C-000610-P46-0031 : EPAR - Assessment Report

    variation-report · 2024-12-13 · EMA/420915/2024

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  • Noxafil-H-C-610-PSUSA-00002480-202310 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation

    scientific-conclusion · 2024-09-06 · EMA/375776/2024

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  • Noxafil-H-C-610-X-0063-G : EPAR - Assessment Report - Variation

    variation-report · 2022-01-26 · EMA/702418/2021

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  • Noxafil-H-C-610-II-0062 : EPAR - Assessment Report - Variation

    variation-report · 2021-12-07 · EMA/590500/2021

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  • Noxafil-H-C-610-PSUSA-00002480-202010 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation

    scientific-conclusion · 2021-08-30 · EMA/332925/2021

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  • Noxafil-H-C-610-P46-0030 : EPAR - Assessment Report

    variation-report · 2020-09-29 · EMA/382050/2020

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  • Noxafil-H-C-610-P46-0029 : EPAR - Assessment Report

    variation-report · 2019-10-09 · EMA/507864/2019

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  • Noxafil-H-C-610-X-0033 : EPAR - Assessment Report - Variation

    variation-report · 2015-02-04 · EMA/CHMP/75051/2015

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  • Noxafil-H-C-610-X-0028 : EPAR - Scientific Discussion - Extension

    variation-report · 2014-06-10 · EMA/159150/2014

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  • Noxafil-H-C-610-II-0002 : EPAR - Scientific Discussion - Variation

    scientific-discussion-variation · 2007-01-15

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  • Noxafil-H-C-610-II-0001 : EPAR - Scientific Discussion - Variation

    scientific-discussion-variation · 2007-01-15

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  • Noxafil : EPAR - Scientific Discussion

    scientific-discussion · 2005-11-04

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  • Noxafil : EPAR - Procedural steps taken before authorisation

    procedural-steps-before · 2005-11-04

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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。