法规知识库 · EMA 集中审评
Lynparza
olaparib · EMEA/H/C/003726 · 已授权
获批上市许可
2014-12-16
欧委会决定日
2026-02-12
持有人 / 申请人
AstraZeneca AB
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
18
assessment / overview 等
产品信息
3
PI / presentations
其他
0
RMP / PIP 等
ATC:L01XK01
治疗领域:Ovarian Neoplasms;Breast Neoplasms;Pancreatic Neoplasms;Prostatic Neoplasms, Castration-Resistant
药理分类:Antineoplastic agents
修订号:32 · 最新影响 PI 的程序:VR/0000296305
适应症(原文):Ovarian cancer Lynparza is indicated as monotherapy for the: maintenance treatment of adult patients with advanced (FIGO stages III and IV) BRCA1/2-mutated (germline and/or somatic) high-grade epithelial ovarian, fallopian tube or primary peritoneal cancer who are in response (complete or partial) following completion of first-line platinum-based chemotherapy. maintenance treatment of adult patients with platinum sensitive relapsed high grade epithelial ovarian, fallopian tube, or primary peritoneal cancer who are in response (complete or partial) to platinum based chemotherapy. Lynparza in combination with bevacizumab is indicated for the: maintenance treatment of adult patients with advanced (FIGO stages III and IV) high-grade epithelial ovarian, fallopian tube or primary peritoneal cancer who are in response (complete or partial) following completion of first-line platinum-based chemotherapy in combination with bevacizumab and whose cancer is associated with homologous recombination deficiency (HRD) positive status defined by either a BRCA1/2 mutation and/or genomic instability (see section 5.1). Breast cancer Lynparza is indicated as: monotherapy or in combination with endocrine therapy for the adjuvant treatment of adult patients with germline BRCA1/2-mutations who have HER2-negative, high risk early breast cancer previously treated with neoadjuvant or adjuvant chemotherapy (see sections 4.2 and 5.1). monotherapy for the treatment of adult patients with germline BRCA1/2-mutations, who have HER2 negative locally advanced or metastatic breast cancer. Patients should have previously been treated with an anthracycline and a taxane in the (neo)adjuvant or metastatic setting unless patients were not suitable for these treatments (see section 5.1). Patients with hormone receptor (HR)-positive breast cancer should also have progressed on or after prior endocrine therapy, or be considered unsuitable for endocrine therapy. Adenocarcinoma of the pancreas Lynparza is indicated as: monotherapy for the maintenance treatment of adult patients with germline BRCA1/2-mutations who have metastatic adenocarcinoma of the pancreas and have not progressed after a minimum of 16 weeks of platinum treatment within a first-line chemotherapy regimen. Prostate cancer Lynparza is indicated as: monotherapy for the treatment of adult patients with metastatic castration-resistant prostate cancer (mCRPC) and BRCA1/2-mutations (germline and/or somatic) who have progressed following prior therapy that included a new hormonal agent. in combination with abiraterone and prednisone or prednisolone for the treatment of adult patients with mCRPC in whom chemotherapy is not clinically indicated (see section 5.1). Endometrial cancer Lynparza in combination with durvalumab is indicated for the maintenance treatment of adult patients with primary advanced or recurrent endometrial cancer that is mismatch repair proficient (pMMR) whose disease has not progressed on first-line treatment with durvalumab in combination with carboplatin and paclitaxel.
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。
2026-02-12 · 欧委会决定
2014-12-16 · 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
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Lynparza : EPAR - Risk management plan
rmp · 2026-08-12
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Lynparza : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan
pip-compliance · 2026-06-03 · EMADOC-1700519818-3211686
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Lynparza : EPAR - Procedural steps taken and scientific information after authorisation
procedural-steps-after · 2026-06-03
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Lynparza-H-C-WS2463 : EPAR - Assessment Report - Variation
variation-report · 2026-03-19 · EMA/346655/2024
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Lynparza-VR-0000287658 : EPAR - Assessment report - Variation
variation-report · 2025-12-04 · EMADOC-1700519818-2335536
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Lynparza-H-C-3726-II-0051-G : EPAR - Assessment Report - Variation
variation-report · 2025-10-15 · EMA/CHMP/566771/2022
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Lynparza : EPAR - Procedural steps taken and scientific information after authorisation (archive)
procedural-steps-after · 2025-07-18
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Lynparza : EPAR - Medicine overview
overview · 2024-09-02 · EMA/889990/2022
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Lynparza-H-C-3726-II-0053 : EPAR - Assessment Report - Variation
variation-report · 2023-02-02 · EMA/941572/2022
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Lynparza-H-C-3726-II-0035 : EPAR - Assessment Report - Variation
variation-report · 2020-11-06 · EMA/523504/2020
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Lynparza-H-C-3726-II-0036 : EPAR - Assessment Report - Variation
variation-report · 2020-11-06 · EMA/541236/2020
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Lynparza-H-C-PSUSA-00010322-201912 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation
scientific-conclusion · 2020-10-06 · EMA/381415/2020
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Lynparza-H-C-003726-II-0033 : EPAR - Assessment Report - Variation
variation-report · 2020-07-28 · EMA/195425/2020
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Lynparza-H-C-003726-II-0023 : EPAR - Assessment Report - Variation
variation-report · 2019-07-11 · EMA/330530/2019
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Lynparza-H-C-3726-II-0020 : EPAR - Assessment Report - Variation
variation-report · 2019-06-04 · EMA/208498/2019
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Lynparza : Orphan designation withdrawal assessment report (post-authorisation)
orphan-maintenance-report-post · 2018-05-28 · EMA/214775/2018
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Lynparza-H-C-3726-X-0016-G : EPAR - Assessment Report - Extension
variation-report · 2018-05-28 · EMA/64964/2018
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Lynparza : EPAR - Public assessment report
assessment-report · 2015-01-09 · EMA/CHMP/789139/2014
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。