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法规知识库 · EMA 集中审评

Simponi

golimumab · EMEA/H/C/000992 · 已授权

获批上市许可

2009-10-01

欧委会决定日

2026-01-19

持有人 / 申请人

Janssen Cilag International NV

终止日期字段

无

从产品到官方文件

文件记录

20

官方索引 20

EPAR / 审评

17

assessment / overview 等

产品信息

3

PI / presentations

其他

0

RMP / PIP 等

ATC:L04AB06

治疗领域:Arthritis, Psoriatic;Spondylitis, Ankylosing;Colitis, Ulcerative;Arthritis, Rheumatoid

药理分类:Immunosuppressants

修订号:54 · 最新影响 PI 的程序:II/0121

适应症(原文):Rheumatoid arthritis (RA) Simponi, in combination with methotrexate (MTX), is indicated for: the treatment of moderate to severe, active rheumatoid arthritis in adults when the response to disease modifying anti rheumatic drug (DMARD) therapy including MTX has been inadequate. the treatment of severe, active and progressive rheumatoid arthritis in adults not previously treated with MTX. Simponi, in combination with MTX, has been shown to reduce the rate of progression of joint damage as measured by X ray and to improve physical function. For information regarding the polyarticular juvenile idiopathic arthritis indication, please see the Simponi 50 mg SmPC. Psoriatic arthritis (PsA) Simponi, alone or in combination with MTX, is indicated for the treatment of active and progressive psoriatic arthritis in adult patients when the response to previous DMARD therapy has been inadequate. Simponi has been shown to reduce the rate of progression of peripheral joint damage as measured by X ray in patients with polyarticular symmetrical subtypes of the disease (see section 5.1) and to improve physical function. Axial spondyloarthritis Ankylosing spondylitis (AS) Simponi is indicated for the treatment of severe, active ankylosing spondylitis in adults who have responded inadequately to conventional therapy. Non radiographic axial spondyloarthritis (nr Axial SpA) Simponi is indicated for the treatment of adults with severe, active non radiographic axial spondyloarthritis with objective signs of inflammation as indicated by elevated C reactive protein (CRP) and/or magnetic resonance imaging (MRI) evidence, who have had an inadequate response to, or are intolerant to nonsteroidal anti-inflammatory drugs (NSAIDs). Ulcerative colitis (UC) Simponi is indicated for treatment of moderately to severely active ulcerative colitis in adult patients who have had an inadequate response to conventional therapy including corticosteroids and 6 mercaptopurine (6 MP) or azathioprine (AZA), or who are intolerant to or have medical contraindications for such therapies. Ulcerative colitisPaediatric ulcerative colitis (pUC)Simponi is indicated for the treatment of moderately to severely active ulcerative colitis in paediatric patients 2 years of age and older with a body weight of at least 15 kg, who have had an inadequate response to conventional therapy, including corticosteroids and 6‑mercaptopurine (6‑MP) or azathioprine (AZA), or who are intolerant to or have medical contraindications for such therapies. Juvenile idiopathic arthritis Polyarticular juvenile idiopathic arthritis (pJIA) Simponi in combination with methotrexate (MTX) is indicated for the treatment of polyarticular juvenile idiopathic arthritis in children 2 years of age and older, who have responded inadequately to previous therapy with MTX. Rheumatoid arthritis (RA) Simponi, in combination with methotrexate (MTX), is indicated for: the treatment of moderate to severe, active rheumatoid arthritis in adults when the response to disease modifying anti rheumatic drug (DMARD) therapy including MTX has been inadequate. the treatment of severe, active and progressive rheumatoid arthritis in adults not previously treated with MTX. Simponi, in combination with MTX, has been shown to reduce the rate of progression of joint damage as measured by X ray and to improve physical function. Juvenile idiopathic arthritis Polyarticular juvenile idiopathic arthritis (pJIA) Simponi in combination with MTX is indicated for the treatment of polyarticular juvenile idiopathic arthritis in children 2 years of age and older, who have responded inadequately to previous therapy with MTX. Psoriatic arthritis (PsA) Simponi, alone or in combination with MTX, is indicated for the treatment of active and progressive psoriatic arthritis in adult patients when the response to previous DMARD therapy has been inadequate. Simponi has been shown to reduce the rate of progression of peripheral joint damage as measured by X ray in patients with polyarticular symmetrical subtypes of the disease (see section 5.1) and to improve physical function. Axial spondyloarthritis Ankylosing spondylitis (AS) Simponi is indicated for the treatment of severe, active ankylosing spondylitis in adults who have responded inadequately to conventional therapy. Non radiographic axial spondyloarthritis (nr Axial SpA) Simponi is indicated for the treatment of adults with severe, active non radiographic axial spondyloarthritis with objective signs of inflammation as indicated by elevated C reactive protein (CRP) and/or magnetic resonance imaging (MRI) evidence, who have had an inadequate response to, or are intolerant to nonsteroidal anti-inflammatory drugs (NSAIDs). Ulcerative colitis (UC) Simponi is indicated for treatment of moderately to severely active ulcerative colitis in adult patients who have had an inadequate response to conventional therapy including corticosteroids and 6 mercaptopurine (6 MP) or azathioprine (AZA), or who are intolerant to or have medical contraindications for such therapies.

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. 2026-01-19 · 欧委会决定

  2. 2009-10-01 · 获批上市许可

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 17产品信息 3其他 0

EPAR / 审评资料

  • Simponi : EPAR - Medicine overview

    overview · 2026-03-05 · EMA/45820/2026

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  • Simponi-H-C-000992-II-0121 : EPAR - Assessment report

    variation-report · 2026-01-30 · EMA/8289/2026

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  • Simponi : EPAR - Risk management plan

    rmp · 2026-01-30

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

    procedural-steps-after · 2026-01-30

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  • Simponi-H-C-000992-II-0113 : EPAR - Assessment report

    variation-report · 2026-01-21 · EMA/390341/2025

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

    procedural-steps-after · 2025-10-15

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  • Simponi-H-C-992-P46-038 : EPAR - Assessment Report

    variation-report · 2022-01-28 · EMA/531598/2021

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  • Simponi-H-C-992-P46-037 : EPAR - Assessment Report

    variation-report · 2021-11-16 · EMA/527502/2021

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  • Simponi-H-C-992-X-0083-G: EPAR - Assessment Report - Extension

    variation-report · 2019-03-13 · EMA/898638/2018

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  • Simponi-H-C-992-II-0063 : EPAR - Assessment Report - Variation

    variation-report · 2016-08-11 · EMA/CHMP/404217/2016

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  • Simponi-H-C-992-II-0061 : EPAR - Assessment Report - Variation

    variation-report · 2015-08-12 · EMA/CHMP/422136/2015

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  • Simponi-H-C-992-PSUV-0058: EPAR - Scientific conclusions and grounds recommending the variation to the terms of the marketing authorisation

    scientific-conclusion · 2015-02-05 · EMA/CHMP/81751/2015

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  • Simponi-H-C-992-II-0039 : EPAR - Assessment Report - Variation

    variation-report · 2013-10-23 · EMA/640422/2013

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  • Simponi-H-C-992-II-0025: EPAR - Assessment Report - Variation

    variation-report · 2011-07-20

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  • Simponi-H-C-992-II-0008: EPAR - Assessment Report- Variation

    variation-report · 2011-02-18 · EMA/CHMP/58067/2011

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  • Simponi : EPAR - Conditions imposed on member states for safe and effective use - Annex IV

    conditions-member-states · 2009-10-20

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  • Simponi : EPAR - Public assessment report

    assessment-report · 2009-10-20

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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。