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法规知识库 · EMA 集中审评

Viread

tenofovir disoproxil fumarate · EMEA/H/C/000419 · 已授权

获批上市许可

2002-02-04

欧委会决定日

2024-02-16

持有人 / 申请人

Gilead Sciences Ireland UC

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

19

assessment / overview 等

产品信息

2

PI / presentations

其他

0

RMP / PIP 等

ATC:J05AF07

治疗领域:Hepatitis B, Chronic;HIV Infections

药理分类:Antivirals for systemic use

修订号:61 · 最新影响 PI 的程序:PSUSA/2892/202303

适应症(原文):HIV 1 infection Viread 123 mg film coated tablets are indicated in combination with other antiretroviral medicinal products for the treatment of HIV 1 infected paediatric patients, with NRTI resistance or toxicities precluding the use of first line agents, aged 6 to < 12 years who weigh from 17 kg to less than 22 kg. The choice of Viread to treat antiretroviral experienced patients with HIV 1 infection should be based on individual viral resistance testing and/or treatment history of patients. Hepatitis B infection Viread 123 mg film coated tablets are indicated for the treatment of chronic hepatitis B in paediatric patients aged 6 to < 12 years who weigh from 17 kg to less than 22 kg, with compensated liver disease and evidence of immune active disease, i.e. active viral replication and persistently elevated serum ALT levels, or histological evidence of moderate to severe inflammation and/or fibrosis.  With respect to the decision to initiate treatment in paediatric patients, see sections 4.2, 4.4, 4.8 and 5.1. HIV 1 infection Viread 163 mg film coated tablets are indicated in combination with other antiretroviral medicinal products for the treatment of HIV 1 infected paediatric patients, with NRTI resistance or toxicities precluding the use of first line agents, aged 6 to < 12 years who weigh from 22 kg to less than 28 kg. The choice of Viread to treat antiretroviral experienced patients with HIV 1 infection should be based on individual viral resistance testing and/or treatment history of patients. Hepatitis B infection Viread 163 mg film coated tablets are indicated for the treatment of chronic hepatitis B in paediatric patients aged 6 to < 12 years who weigh from 22 kg to less than 28 kg, with: compensated liver disease and evidence of immune active disease, i.e. active viral replication and persistently elevated serum ALT levels, or histological evidence of moderate to severe inflammation and/or fibrosis.  With respect to the decision to initiate treatment in paediatric patients, see sections 4.2, 4.4, 4.8 and 5.1. HIV 1 infection Viread 204 mg film coated tablets are indicated in combination with other antiretroviral medicinal products for the treatment of HIV 1 infected paediatric patients, with NRTI resistance or toxicities precluding the use of first line agents, aged 6 to < 12 years who weigh from 28 kg to less than 35 kg. The choice of Viread to treat antiretroviral experienced patients with HIV 1 infection should be based on individual viral resistance testing and/or treatment history of patients. Hepatitis B infection Viread 204 mg film coated tablets are indicated for the treatment of chronic hepatitis B in paediatric patients aged 6 to < 12 years who weigh from 28 kg to less than 35 kg, with: compensated liver disease and evidence of immune active disease, i.e. active viral replication and persistently elevated serum ALT levels or histological evidence of moderate to severe inflammation and/or fibrosis.  With respect to the decision to initiate treatment in paediatric patients, see sections 4.2, 4.4, 4.8 and 5.1. HIV 1 infection Viread 245 mg film coated tablets are indicated in combination with other antiretroviral medicinal products for the treatment of HIV 1 infected adults. In adults, the demonstration of the benefit of Viread in HIV 1 infection is based on results of one study in treatment naïve patients, including patients with a high viral load (> 100,000 copies/ml) and studies in which Viread was added to stable background therapy (mainly tritherapy) in antiretroviral pre-treated patients experiencing early virological failure (< 10,000 copies/ml, with the majority of patients having < 5,000 copies/ml). Viread 245 mg film coated tablets are also indicated for the treatment of HIV 1 infected adolescents, with NRTI resistance or toxicities precluding the use of first line agents, aged 12 to < 18 years. The choice of Viread to treat antiretroviral experienced patients with HIV 1 infection should be based on individual viral resistance testing and/or treatment history of patients. Hepatitis B infection Viread 245 mg film coated tablets are indicated for the treatment of chronic hepatitis B in adults with: compensated liver disease, with evidence of active viral replication, persistently elevated serum alanine aminotransferase (ALT) levels and histological evidence of active inflammation and/or fibrosis (see section 5.1). evidence of lamivudine resistant hepatitis B virus (see sections 4.8 and 5.1). decompensated liver disease (see sections 4.4, 4.8 and 5.1). Viread 245 mg film coated tablets are indicated for the treatment of chronic hepatitis B in adolescents 12 to < 18 years of age with: compensated liver disease and evidence of immune active disease, i.e. active viral replication and persistently elevated serum ALT levels, or histological evidence of moderate to severe inflammation and/or fibrosis.  With respect to the decision to initiate treatment in paediatric patients, see sections 4.2, 4.4, 4.8 and 5.1. HIV 1 infection Viread 33 mg/g granules are indicated in combination with other antiretroviral medicinal products for the treatment of HIV 1 infected paediatric patients, with NRTI resistance or toxicities precluding the use of first line agents, from 2 to < 6 years of age, and above 6 years of age for whom a solid dosage form is not appropriate. Viread 33 mg/g granules are also indicated in combination with other antiretroviral medicinal products for the treatment of HIV 1 infected adults for whom a solid dosage form is not appropriate. In adults, the demonstration of the benefit of Viread in HIV 1 infection is based on results of one study in treatment naïve patients, including patients with a high viral load (> 100,000 copies/ml) and studies in which Viread was added to stable background therapy (mainly tritherapy) in antiretroviral pre-treated patients experiencing early virological failure (< 10,000 copies/ml, with the majority of patients having < 5,000 copies/ml). The choice of Viread to treat antiretroviral experienced patients with HIV 1 infection should be based on individual viral resistance testing and/or treatment history of patients. Hepatitis B infection Viread 33 mg/g granules are indicated for the treatment of chronic hepatitis B in adults for whom a solid dosage form is not appropriate with: compensated liver disease, with evidence of active viral replication, persistently elevated serum alanine aminotransferase (ALT) levels and histological evidence of active inflammation and/or fibrosis (see section 5.1). evidence of lamivudine resistant hepatitis B virus (see sections 4.8 and 5.1). decompensated liver disease (see sections 4.4, 4.8 and 5.1). Viread 33 mg/g granules are also indicated for the treatment of chronic hepatitis B in paediatric patients2 to < 18 years of age for whom a solid dosage form is not appropriate with: compensated liver disease and evidence of immune active disease, i.e. active viral replication, and persistently elevated serum ALT levels, or histological evidence of moderate to severe inflammation and/or fibrosis.  With respect to the decision to initiate treatment in paediatric patients, see sections 4.2, 4.4, 4.8 and 5.1.

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. 2024-02-16 · 欧委会决定

  2. 2008-03-19 · CHMP 意见通过

  3. 2002-02-04 · 获批上市许可

说明书、EPAR 与其他文件

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EPAR / 审评资料 19产品信息 2其他 0

EPAR / 审评资料

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

    procedural-steps-after · 2025-11-18

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  • Viread : EPAR - Risk management plan

    rmp · 2025-11-18

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

    procedural-steps-after · 2025-11-18

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  • Viread-H-C-PSUSA-00002892-202303 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation

    scientific-conclusion · 2024-02-29 · EMA/75726/2024

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  • Viread-PSUSA-00002892-201903 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation

    scientific-conclusion · 2020-04-03 · EMA/134602/2020

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  • Viread-H-C-419-II-0191 : EPAR - Assessment Report - Variation

    variation-report · 2019-05-16 · EMA/239040/2019

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  • Viread : EPAR - Medicine overview

    overview · 2019-05-16 · EMA/184130/2019

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  • Viread-H-C-419-P46-0249 : EPAR - Assessment Report

    variation-report · 2015-01-05 · EMA/801575/2014

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  • Viread-H-C-419-P46-0243 : EPAR - Assessment Report

    variation-report · 2013-09-06 · EMA/527973/2013

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  • Viread-H-C-419-II-0120 : EPAR - Assessment Report - Variation

    variation-report · 2013-09-06 · EMA/527625/2013

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  • Viread-H-C-419-II-0119 : EPAR - Assessment Report - Variation

    variation-report · 2012-12-13 · EMA/797673/2012

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  • Viread-H-C-419-II-0115 : EPAR - Assessment Report - Variation

    variation-report · 2012-12-13 · EMA/797672/2012

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  • Viread-H-C-419-X-0105-G : EPAR - Assessment Report - Extension

    variation-report · 2012-12-13 · EMA/797671/2012

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  • Viread-H-C-419-II-0098 : EPAR - Assessment Report - Variation

    variation-report · 2011-04-26 · EMEA/H/C/000419/II/0098

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  • Viread-H-C-419-II-0097 : EPAR - Assessment Report - Variation

    variation-report · 2010-10-29 · EMA/562111/2010

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  • Viread-H-C-419-II-0075 : EPAR - Assessment Report - Variation

    variation-report · 2008-05-27 · EMEA/H/C/419/II/75

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  • Viread : EPAR - Steps taken after authorisation when a cutoff date has been used

    steps-after-cutoff · 2006-04-06

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  • Viread : EPAR - Procedural steps taken before authorisation

    procedural-steps-before · 2006-04-06

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  • Viread : EPAR - Scientific Discussion

    scientific-discussion · 2006-04-06

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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。