法规知识库 · EMA 集中审评
Pegasys
peginterferon alfa-2a · EMEA/H/C/000395 · 已授权
获批上市许可
2002-06-20
欧委会决定日
2026-09-22
持有人 / 申请人
pharmaand GmbH
终止日期字段
无
从产品到官方文件
文件记录
18
官方索引 18
EPAR / 审评
16
assessment / overview 等
产品信息
2
PI / presentations
其他
0
RMP / PIP 等
ATC:L03AB11
治疗领域:Hepatitis C, Chronic;Hepatitis B, Chronic;Polycythemia Vera;Thrombocythemia, Essential
药理分类:Immunostimulants
修订号:49 · 最新影响 PI 的程序:VR/0000368501
适应症(原文):Polycythaemia veraPegasys is indicated as monotherapy in adults for the treatment of polycythaemia vera. Essential thrombocythaemiaPegasys is indicated as monotherapy in adults for the treatment of essential thrombocythaemia..Chronic hepatitis BAdult patientsPegasys is indicated for the treatment of hepatitis B envelope antigen (HBeAg)-positive or HBeAg-negative chronic hepatitis B (CHB) in adult patients with compensated liver disease and evidence of viral replication, increased alanine aminotransferase (ALT) and histologically verified liver inflammation and/or fibrosis (see sections 4.4 and 5.1).Paediatric patients 3 years of age and olderPegasys is indicated for the treatment of HBeAg-positive CHB in non-cirrhotic children and adolescents 3 years of age and older with evidence of viral replication and persistently elevated serum ALT levels. With respect to the decision to initiate treatment in paediatric patients see sections 4.2, 4.4 and 5.1.Chronic hepatitis CAdult patientsPegasys is indicated in combination with other medicinal products, for the treatment of chronic hepatitis C (CHC) in patients with compensated liver disease (see sections 4.2, 4.4 and 5.1). For hepatitis C virus (HCV) genotype specific activity, see sections 4.2 and 5.1.Paediatric patients 5 years of age and olderPegasys in combination with ribavirin is indicated for the treatment of CHC in treatment-naïve children and adolescents 5 years of age and older who are positive for serum HCV-RNA.When deciding to initiate treatment in childhood, it is important to consider growth inhibition induced by combination therapy. The reversibility of growth inhibition is uncertain. The decision to treat should be made on a case by case basis (see section 4.4).
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。
2026-09-22 · 欧委会决定
2002-06-20 · 获批上市许可
2002-03-21 · 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
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Pegasys : EPAR - Procedural steps taken and scientific information after authorisation
procedural-steps-after · 2026-09-22
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Pegasys : EPAR - Procedural steps taken and scientific information after authorisation (archive)
procedural-steps-after · 2025-11-05
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Pegasys : EPAR - Risk management plan
rmp · 2024-09-04
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Pegasys-H-C-000395-II-0119-G : EPAR - Assessment Report - Variation
variation-report · 2024-09-04 · EMA/326584/2024
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Pegasys : EPAR - Medicine overview
overview · 2024-09-04 · EMA/336203/2024
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Pegasys-H-C-395-P46-057: EPAR - Assessment report
variation-report · 2020-11-05 · EMA/578690/2020
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Pegasys-H-C-395-II-0091 : EPAR - Assessment Report - Variation
variation-report · 2018-02-05 · EMA/CHMP/54377/2018
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Pegasys-H-C-395-P46-053: EPAR - Assessment report
variation-report · 2016-12-13
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Pegasys-H-C-395-PSUV-0072 : EPAR - Scientific conclusions and grounds recommending the variation to the terms of the marketing authorisation
scientific-conclusion · 2014-06-23 · EMA/CHMP/51083/2014
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Pegasys-H-C-395-II-0073 : EPAR - Assessment Report - Variation
variation-report · 2014-06-23 · EMA/CHMP/231978/2014
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Pegasys-H-C-395-X-0059 : EPAR - Assessment Report - Extension
variation-report · 2013-03-22 · EMA/CHMP/83314/2013
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Pegasys-H-C-395-A20-0060 : EPAR - Assessment Report - Article 20
variation-report · 2012-11-21 · EMA/568026/2012
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Pegasys-H-C-395-II-0036 : EPAR - Assessment Report - Variation
variation-report · 2008-12-18
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Pegasys : EPAR - Scientific Discussion
scientific-discussion · 2006-08-08
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Pegasys : EPAR - Procedural steps taken before authorisation
procedural-steps-before · 2006-08-08
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Pegasys : EPAR - Steps taken after authorisation when a cutoff date has been used
steps-after-cutoff · 2006-08-08
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。