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欧盟委员会批准Tevimbra联合疗法用于鼻咽癌治疗

European Commission Approves Tevimbra Combination Therapy for Nasopharyngeal Carcinoma Treatment

GeneOnline 等信源发布 2025-07-14 18:05

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by Mark Chiang

马克·蒋

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The European Commission has granted approval for Tevimbra (tislelizumab), developed by BeOne Medicines, to be used in combination with gemcitabine and cisplatin for the treatment of nasopharyngeal carcinoma (NPC). This decision allows the use of Tevimbra as part of a therapeutic regimen targeting adult patients diagnosed with this specific type of cancer..

欧盟委员会已批准百济神州开发的Tevimbra(替雷利珠单抗)与吉西他滨和顺铂联合使用,用于治疗鼻咽癌(NPC)。这一决定允许将Tevimbra作为针对成年患者的特定类型癌症治疗方案的一部分。

Nasopharyngeal carcinoma is a rare form of cancer that originates in the nasopharynx, located behind the nose and above the back of the throat. The approved combination therapy includes Tevimbra, an anti-PD-1 monoclonal antibody, alongside gemcitabine and cisplatin, which are established chemotherapy agents.

鼻咽癌是一种罕见的癌症,起源于位于鼻子后方和喉咙后上方的鼻咽。获批的联合疗法包括抗PD-1单克隆抗体Tevimbra,以及已确立的化疗药物吉西他滨和顺铂。

The approval follows a review process by regulatory authorities assessing its safety and efficacy in treating NPC..

该批准是在监管机构对其治疗鼻咽癌的安全性和有效性进行审查程序后作出的。

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Source: GO-AI-ne1

来源:GO-AI-ne1

Date: July 11, 2025

日期:2025年7月11日

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Mark Chiang

马克·江

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