法规知识库 · EMA 集中审评
Tevimbra
tislelizumab · EMEA/H/C/005919 · 已授权
获批上市许可
2023-09-15
欧委会决定日
2026-09-18
持有人 / 申请人
Beone Medicines Ireland Limited
终止日期字段
无
从产品到官方文件
文件记录
17
官方索引 17
EPAR / 审评
15
assessment / overview 等
产品信息
2
PI / presentations
其他
0
RMP / PIP 等
ATC:L01FF09
治疗领域:Esophageal Squamous Cell Carcinoma;Carcinoma, Non-Small-Cell Lung;Small Cell Lung Carcinoma;Nasopharyngeal Carcinoma;Stomach Neoplasms
药理分类:Antineoplastic agents
修订号:18 · 最新影响 PI 的程序:PSUR/0000336087
适应症(原文):Non-small cell lung cancer (NSCLC) Tevimbra, in combination with platinum-containing chemotherapy as neoadjuvant treatment and then continued as monotherapy as adjuvant treatment, is indicated for the treatment of adult patients with resectable NSCLC at high risk of recurrence (for selection criteria, see section 5.1).Tevimbra in combination with pemetrexed and platinum containing chemotherapy is indicated for the first-line treatment of adult patients with non-squamous NSCLC whose tumours have PD-L1 expression on ≥50% of tumour cells with no EGFR or ALK positive mutations and who have: locally advanced NSCLC and are not candidates for surgical resection or platinum-based chemoradiation, or metastatic NSCLC. Tevimbra in combination with carboplatin and either paclitaxel or nab-paclitaxel is indicated for the first-line treatment of adult patients with squamous NSCLC who have: locally advanced NSCLC and are not candidates for surgical resection or platinum-based chemoradiation, or metastatic NSCLC. Tevimbra as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic NSCLC after prior platinum-based therapy. Patients with EGFR mutant or ALK positive NSCLC should also have received targeted therapies before receiving tislelizumab. Small Cell Lung Cancer (SCLC)Tevimbra, in combination with etoposide and platinum chemotherapy, is indicated for the first-line treatment of adult patients with extensive-stage SCLC. Gastric or gastroesophageal junction (G/GEJ) adenocarcinomaTevimbra, in combination with platinum and fluoropyrimidine-based chemotherapy, is indicated for the first-line treatment of adult patients with HER-2-negative locally advanced unresectable or metastatic gastric or gastroesophageal junction (G/GEJ) adenocarcinoma whose tumours express PD L1 with a tumour area positivity (TAP) score ≥ 5% (see section 5.1).Oesophageal squamous cell carcinoma (OSCC)Tevimbra, in combination with platinum-based chemotherapy, is indicated for the first-line treatment of adult patients with unresectable, locally advanced or metastatic OSCC whose tumours express PD L1 with a TAP score ≥ 5% (see section 5.1).Tevimbra as monotherapy is indicated for the treatment of adult patients with unresectable, locally advanced or metastatic OSCC after prior platinum-based chemotherapy. Nasopharyngeal carcinoma (NPC)Tevimbra, in combination with gemcitabine and cisplatin, is indicated for the first-line treatment of adult patients with recurrent, not amenable to curative surgery or radiotherapy, or metastatic NPC.
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。
2026-09-18 · 欧委会决定
2023-09-15 · 获批上市许可
2023-07-20 · 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
- 打开官方文件 ↗
Tevimbra-PSUSA-00000136-202512 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation
scientific-conclusion · 2026-09-24 · EMADOC-1700519818-3467463
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Tevimbra : EPAR - Procedural steps taken and scientific information after authorisation
procedural-steps-after · 2026-09-24
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Tevimbra : EPAR - Risk management plan
rmp · 2026-09-24
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Tevimbra-PSUSA-00000136-202412 : Scientific conclusions and grounds for the variation to the terms of the marketing authorisation
scientific-conclusion · 2026-01-26 · EMADOC-1700519818-2853292
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Tevimbra : EPAR - Medicine overview
overview · 2025-11-12 · EMA/193656/2025
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Tevimbra-H-C-005919-II-0018 : EPAR - Assessment report - Variation
variation-report · 2025-09-16 · EMA/CHMP/212902/2025
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Tevimbra : EPAR - Procedural steps taken and scientific information after authorisation (archive)
procedural-steps-after · 2025-09-16
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Tevimbra-H-C-005919-II-0017 : EPAR - Assessment report - Variation
variation-report · 2025-07-31 · EMA/CHMP/194012/2025
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Tevimbra-H-C-005919-II-0016 : EPAR - Assessment report - Variation
variation-report · 2025-05-20 · EMA/CHMP/136727/2025
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Tevimbra-H-C-PSUSA-00000136-202406 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation
scientific-conclusion · 2025-04-23 · EMA/139530/2025
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Tevimbra-H-C-005919-II-0003 : EPAR - Assessment report - Variation
variation-report · 2024-12-19 · EMA/510875/2024
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Tevimbra-H-C-005919-II-0006 : EPAR - Assessment report - Variation
variation-report · 2024-12-19 · EMA/510873/2024
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Tevimbra-H-C-005919-II-0008 : EPAR - Assessment report - Variation
variation-report · 2024-07-25 · EMA/294229/2024
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Tevimbra : EPAR - Orphan maintenance assessment report
orphan-maintenance-report · 2023-10-10 · EMA/OD/0000129253
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Tevimbra : EPAR - Public assessment report
assessment-report · 2023-10-02 · EMA/CHMP/359838/2023
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。