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法规知识库 · EMA 集中审评

Opdivo

nivolumab · EMEA/H/C/003985 · 已授权

获批上市许可

2015-06-19

欧委会决定日

2026-10-16

持有人 / 申请人

Bristol-Myers Squibb Pharma EEIG

终止日期字段

无

从产品到官方文件

文件记录

50

官方索引 50

EPAR / 审评

48

assessment / overview 等

产品信息

2

PI / presentations

其他

0

RMP / PIP 等

ATC:L01FF01

治疗领域:Melanoma;Hodgkin Disease;Carcinoma, Renal Cell;Carcinoma, Non-Small-Cell Lung;Carcinoma, Transitional Cell;Squamous Cell Carcinoma of Head and Neck;Urologic Neoplasms;Mesothelioma;Colorectal Neoplasms

药理分类:Antineoplastic agents

修订号:77 · 最新影响 PI 的程序:VR/0000372659

适应症(原文):Melanoma Opdivo as monotherapy or in combination with ipilimumab is indicated for the treatment of advanced (unresectable or metastatic) melanoma in adults and adolescents 12 years of age and older.Relative to nivolumab monotherapy, an increase in progression-free survival (PFS) and overall survival (OS) for the combination of nivolumab with ipilimumab is established only in patients with low tumour PD-L1 expression (see sections 4.4 and 5.1). Adjuvant treatment of melanoma Opdivo as monotherapy is indicated for the adjuvant treatment of adults and adolescents 12 years of age and older with Stage IIB or IIC melanoma, or melanoma with involvement of lymph nodes or metastatic disease who have undergone complete resection (see section 5.1). Non-small cell lung cancer (NSCLC) Opdivo in combination with ipilimumab and 2 cycles of platinum-based chemotherapy is indicated for the first-line treatment of metastatic non-small cell lung cancer in adults whose tumours have no sensitising EGFR mutation or ALK translocation. Opdivo as monotherapy is indicated for the treatment of locally advanced or metastatic non-small cell lung cancer after prior chemotherapy in adults. Neoadjuvant treatment of NSCLC Opdivo in combination with platinum-based chemotherapy is indicated for the neoadjuvant treatment of resectable non-small cell lung cancer at high risk of recurrence in adult patients whose tumours have PD-L1 expression ≥ 1% (see section 5.1 for selection criteria). Neoadjuvant and adjuvant treatment of NSCLC Opdivo, in combination with platinum-based chemotherapy as neoadjuvant treatment, followed by OPDIVO as monotherapy as adjuvant treatment, is indicated for the treatment of resectable non-small cell lung cancer at high risk of recurrence in adult patients whose tumours have PD-L1 expression ≥ 1% (see section 5.1 for selection criteria). Malignant pleural mesothelioma (MPM) Opdivo in combination with ipilimumab is indicated for the first-line treatment of adult patients with unresectable malignant pleural mesothelioma. Renal cell carcinoma (RCC) Opdivo as monotherapy is indicated for the treatment of advanced renal cell carcinoma after prior therapy in adults. Opdivo in combination with ipilimumab is indicated for the first-line treatment of adult patients with intermediate/poor-risk advanced renal cell carcinoma (see section 5.1). Opdivo in combination with cabozantinib is indicated for the first-line treatment of adult patients with advanced renal cell carcinoma (see section 5.1). Classical Hodgkin lymphoma (cHL) Opdivo in combination with doxorubicin, vinblastine and dacarbazine (AVD) is indicated for adults and adolescents 12 years of age and older with previously untreated Stage III or IV classical Hodgkin lymphoma. Opdivo as monotherapy is indicated for the treatment of adult patients with relapsed or refractory classical Hodgkin lymphoma after autologous stem cell transplant (ASCT) and treatment with brentuximab vedotin. Opdivo in combination with brentuximab vedotin is indicated for the treatment of children 5 years of age and older, adolescents and adults up to 30 years of age with relapsed or refractory classical Hodgkin lymphoma after one prior line of therapy (see section 5.1). Squamous cell cancer of the head and neck (SCCHN) Opdivo as monotherapy is indicated for the treatment of recurrent or metastatic squamous cell cancer of the head and neck in adults progressing on or after platinum-based therapy (see section 5.1). Urothelial carcinoma Opdivo in combination with cisplatin and gemcitabine is indicated for the first-line treatment of adult patients with unresectable or metastatic urothelial carcinoma. Opdivo as monotherapy is indicated for the treatment of locally advanced unresectable or metastatic urothelial carcinoma in adults after failure of prior platinum-containing therapy. Adjuvant treatment of urothelial carcinoma Opdivo as monotherapy is indicated for the adjuvant treatment of adults with muscle invasive urothelial carcinoma (MIUC) with tumour cell PD-L1 expression ≥ 1%, who are at high risk of recurrence after undergoing radical resection of MIUC (see section 5.1). Mismatch repair deficient (dMMR) or microsatellite instability-high (MSI-H) colorectal cancer (CRC) Opdivo in combination with ipilimumab is indicated for the treatment of adult patients with mismatch repair deficient or microsatellite instability-high colorectal cancer in the following settings:- first-line treatment of unresectable or metastatic colorectal cancer;- treatment of metastatic colorectal cancer after prior fluoropyrimidine-based combination chemotherapy (see section 5.1). Oesophageal squamous cell carcinoma (OSCC) Opdivo in combination with ipilimumab is indicated for the first-line treatment of adult patients with unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma with tumour cell PD-L1 expression ≥ 1%. Opdivo in combination with fluoropyrimidine‑ and platinum‑based combination chemotherapy is indicated for the first‑line treatment of adult patients with unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma with tumour cell PD‑L1 expression ≥ 1%. Opdivo as monotherapy is indicated for the treatment of adult patients with unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma after prior fluoropyrimidine‑ and platinum‑based combination chemotherapy. Adjuvant treatment of oesophageal or gastro‑oesophageal junction cancer (OC or GEJC) Opdivo as monotherapy is indicated for the adjuvant treatment of adult patients with oesophageal or gastro‑oesophageal junction cancer who have residual pathologic disease following prior neoadjuvant chemoradiotherapy (see section 5.1). Gastric, gastro‑oesophageal junction (GEJ) or oesophageal adenocarcinoma Opdivo in combination with fluoropyrimidine‑ and platinum‑based combination chemotherapy is indicated for the first‑line treatment of adult patients with HER2‑negative advanced or metastatic gastric, gastro‑oesophageal junction or oesophageal adenocarcinoma whose tumours express PD‑L1 with a combined positive score (CPS) ≥ 5. Hepatocellular carcinoma (HCC) Opdivo in combination with ipilimumab is indicated for the first‑line treatment of adult patients with unresectable or advanced hepatocellular carcinoma.

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. 2026-10-16 · 欧委会决定

  2. 2015-06-19 · 获批上市许可

  3. 2015-04-23 · 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 48产品信息 2其他 0

EPAR / 审评资料

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

    procedural-steps-after · 2026-10-29

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  • Opdivo : EPAR - Risk management plan

    rmp · 2026-08-24

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  • Opdivo : EPAR - Medicine overview

    overview · 2026-06-22 · EMADOC-1829012207-50703

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  • Opdivo-VR-0000304938 : EPAR - Assessment report - Variation

    variation-report · 2026-06-02 · EMADOC-1700519818-3037106

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  • Opdivo-VR-0000282199 : EPAR - Assessment report - Variation

    variation-report · 2026-03-18 · EMADOC-1700519818-2843503

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

    procedural-steps-after · 2025-11-21

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  • Opdivo-H-C-003985-II-0140 : EPAR - Assessment report - Variation

    variation-report · 2025-06-02 · EMA/CHMP/136733/2025

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  • Opdivo-H-C-003985-X-0144 : EPAR - Assessment report - Variation

    variation-report · 2025-06-02 · EMA/CHMP/142870/2025

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  • Opdivo-H-C-PSUSA-00010379-202407 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation

    scientific-conclusion · 2025-05-02 · EMA/148744/2025

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  • Opdivo-H-C-003985-P46-061 : EPAR - Assessment Report - Variation

    variation-report · 2025-04-01 · EMA/44963/2025

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  • Opdivo-H-C-WS-2717 : EPAR - Assessment Report - Variation

    variation-report · 2025-03-17 · EMA/CHMP/59173/2025

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  • Opdivo-H-C-WS-2672 : EPAR - Assessment Report - Variation

    variation-report · 2025-01-13 · EMA/CHMP/554847/2024

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  • Opdivo-H-C-003985-II-0137 : EPAR - Assessment report - Variation

    variation-report · 2024-06-11 · EMA/225115/2024

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  • Opdivo-H-C-003985-X-0132 : EPAR - Assessment report - Variation

    variation-report · 2024-04-04 · EMA/93617/2024

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  • Opdivo-H-C-003985-II-0130 : EPAR - Assessment Report - Variation

    variation-report · 2023-09-08 · EMA/358599/2023

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  • Opdivo-H-C-003985-II-0117 : EPAR - Assessment Report - Variation

    variation-report · 2023-07-18 · EMA/287093/2023

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  • Opdivo-H-C-003985-II-0125-G : EPAR - Assessment Report - Variation

    variation-report · 2023-06-16 · EMA/221123/2023

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  • Opdivo : EPAR - Paediatric investigation plan compliance statement

    pip-compliance · 2023-06-16 · EMA/190289/2023

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  • Opdivo-H-C-PSUSA-00010379-202107 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation

    scientific-conclusion · 2022-05-10 · EMA/178011/2022

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  • Opdivo-H-C-WS-2113 : EPAR - Assessment Report - Variation

    variation-report · 2022-04-20 · EMA/155438/2022

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  • Opdivo-H-C-003985-II-0100 : EPAR - Assessment Report - Variation

    variation-report · 2022-04-20 · EMA/155845/2022

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  • Opdivo-H-C-003985-II-0107 : EPAR - Assessment Report - Variation

    variation-report · 2022-04-20 · EMA/155595/2022

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  • Opdivo-H-C-003985-II-0096 : EPAR - Assessment Report - Variation

    variation-report · 2021-10-29 · EMA/556100/2021

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  • Opdivo-H-C-3985-II-0095 : EPAR - Assessment Report - Variation

    variation-report · 2021-08-03 · EMA/CHMP/395647/2021

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  • Opdivo - H/C/003985/P46/045 : EPAR - Assessment Report - Variation

    variation-report · 2021-07-21 · EMA/400368/2021

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  • Opdivo - H-C-3985-WS-1840 : EPAR - Assessment Report - Variation

    variation-report · 2021-07-07 · EMA/314215/2021

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  • Opdivo - H/C/003985/P46/043 : EPAR - Assessment Report - Variation

    variation-report · 2021-06-18 · EMA/CHMP/125573/2021

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  • Opdivo - EMEA/H/C/WS1881 : EPAR - Assessment Report - Variation

    variation-report · 2021-06-16 · EMA/302322/2021

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  • Opdivo-H-C-PSUSA-00010379-202007 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation

    scientific-conclusion · 2021-05-07 · EMA/244343/2021

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  • Opdivo-H-C-3985-II-0092: EPAR - Assessment report - Variation

    variation-report · 2021-04-21 · EMA/CHMP/159169/2021

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  • Opdivo-H-C-3985-II-0080 : EPAR - Assessment Report - Variation

    variation-report · 2020-12-14 · EMA/CHMP/584553/2020

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  • Opdivo-H-C-3985-WS-1783 : EPAR - Assessment Report - Variation

    variation-report · 2020-11-25 · EMA/CHMP/603938/2020

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  • Opdivo-H-C-PSUSA-00010379-201901 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation

    scientific-conclusion · 2019-10-11 · EMA/449030/2019

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  • Opdivo-H-C-PSUSA-00010379-201807 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)

    scientific-conclusion · 2019-04-04 · EMA/199542/2019

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  • Opdivo-H-C-3985-WS-01278 : EPAR - Assessment Report - Variation

    variation-report · 2019-01-22 · EMA/902855/2019

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  • Opdivo-H-C-3985-II-0041: EPAR - Assessment Report - Variation

    variation-report · 2018-10-25 · EMA/665778/2018

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  • Opdivo-H-C-3985-II-0019: EPAR - Assessment Report - Variation

    variation-report · 2018-10-25 · EMA/CHMP/392346/2017

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  • Opdivo-H-C-PSUSA-00010379-201801 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation

    variation-report · 2018-10-04 · EMA/CHMP/672697/2018

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  • Opdivo-H-C-PSUSA-00010379-201707 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation

    scientific-conclusion · 2018-05-08 · EMA/CHMP/282459/2018

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  • Opdivo-H-C-PSUSA-00010379-201701 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation

    scientific-conclusion · 2017-10-09 · EMA/664231/2017

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  • Opdivo-H-C-PSUSA-00010379-201607 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation

    scientific-conclusion · 2017-06-16 · EMA/387230/2017

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  • Opdivo-H-C-3985-II-0017 : EPAR - Assessment Report - Variation

    variation-report · 2017-06-16 · EMA/CHMP/271863/2017

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  • Opdivo-H-C-3985-II-0012 : EPAR - Assessment report - Variation

    variation-report · 2017-01-20

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  • Opdivo-H-C-3985-II-0003 : EPAR - Assessment Report - Variation

    variation-report · 2016-06-27 · EMA/CHMP/215704/2016

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  • Opdivo-H-C-003985-II-0002 : EPAR - Scientific Discussion - Variation

    variation-report · 2016-05-03 · EMA/246304/2016

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  • Opdivo-H-C-3985-II-0008 : EPAR - Scientific Discussion - Variation

    variation-report · 2016-05-03 · EMA/246304/2016

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  • Opdivo-H-C-3985-II-0001 : EPAR - Assessment Report - Variation

    variation-report · 2015-12-02 · EMA/682492/2015

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  • Opdivo : EPAR - Public assessment report

    assessment-report · 2015-07-16 · EMA/CHMP/76688/2015

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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。