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法规知识库 · EMA 集中审评

Januvia

sitagliptin · EMEA/H/C/000722 · 已授权

获批上市许可

2007-03-20

欧委会决定日

2025-10-30

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

18

官方索引 18

EPAR / 审评

15

assessment / overview 等

产品信息

3

PI / presentations

其他

0

RMP / PIP 等

ATC:A10BH01

治疗领域:Diabetes Mellitus, Type 2

药理分类:Drugs used in diabetes

修订号:35 · 最新影响 PI 的程序:N/0000309219

适应症(原文):For adult patients with type-2 diabetes mellitus, Januvia is indicated to improve glycaemic control: as monotherapy: in patients inadequately controlled by diet and exercise alone and for whom metformin is inappropriate due to contraindications or intolerance; as dual oral therapy in combination with: metformin when diet and exercise plus metformin alone do not provide adequate glycaemic control; a sulphonylurea when diet and exercise plus maximal tolerated dose of a sulphonylurea alone do not provide adequate glycaemic control and when metformin is inappropriate due to contraindications or intolerance; a peroxisome-proliferator-activated-receptor-gamma (PPAR?) agonist (i.e. a thiazolidinedione) when use of a PPAR? agonist is appropriate and when diet and exercise plus the PPAR? agonist alone do not provide adequate glycaemic control; a PPAR? agonist (i.e. a thiazolidinedione) when use of a PPAR? agonist is appropriate and when diet and exercise plus the PPAR? agonist alone do not provide adequate glycaemic control; as triple oral therapy in combination with: a sulphonylurea and metformin when diet and exercise plus dual therapy with these medicinal products do not provide adequate glycaemic control; a PPAR? agonist and metformin when use of a PPAR? agonist is appropriate and when diet and exercise plus dual therapy with these medicinal products do not provide adequate glycaemic control. Januvia is also indicated as add-on to insulin (with or without metformin) when diet and exercise plus stable dose of insulin do not provide adequate glycaemic control.

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. 2025-10-30 · 欧委会决定

  2. 2007-03-20 · 获批上市许可

说明书、EPAR 与其他文件

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EPAR / 审评资料 15产品信息 3其他 0

EPAR / 审评资料

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

    procedural-steps-after · 2025-10-31

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

    procedural-steps-after · 2025-10-31

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  • Januvia-PAM-0000244502 : EPAR - Assessment report

    variation-report · 2025-06-26 · EMADOC-1700519818-1838618

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  • Januvia : EPAR - Risk-management-plan summary

    rmp-summary · 2022-06-30

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  • Januvia : EPAR - Paediatric investigation plan compliance statement

    pip-compliance · 2020-06-26 · EMEA/H/C/000722/IB/0069

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  • Januvia-H-C-PSUSA-00002711-201708 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation

    scientific-conclusion · 2018-06-21 · EMA/423578/2018

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  • Januvia-H-C-PSUSA-00002711-201408 : EPAR - Scientific conclusions and grounds recommending the variation to the terms of the marketing authorisation

    scientific-conclusion · 2015-07-23 · EMA/304624/2015

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  • Januvia-H-C-722-P46-0030 : EPAR - Assessment Report

    variation-report · 2013-04-02 · EMA/190568/2013

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  • Januvia : EPAR - Summary for the public

    overview · 2012-09-25

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  • Januvia-H-C-722-II-0002 : EPAR - Assessment Report - Variation

    variation-report · 2012-04-27

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  • Januvia-H-C-722-II-0011 : EPAR - Assessment Report - Variation

    variation-report · 2009-12-09 · EMEA/777097/2009

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  • Januvia-H-C-722-II-0008 : EPAR - Assessment Report - Variation

    variation-report · 2009-10-09

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  • Januvia-H-C-722-II-0007 : EPAR - Assessment Report - Variation

    variation-report · 2009-07-06

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  • Januvia : EPAR - Scientific Discussion

    scientific-discussion · 2007-03-26

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  • Januvia : EPAR - Procedural steps taken before authorisation

    procedural-steps-before · 2007-03-26

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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。