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那度鲁胺:首次批准

Nadofaragene Firadenovec: First Approval.

机构信息

Springer Nature, Mairangi Bay, Private Bag 65901, Auckland, 0754, New Zealand.

出版信息

Drugs. 2023 Mar;83(4):353-357. doi: 10.1007/s40265-023-01846-z.

Abstract

Nadofaragene firadenovec (nadofaragene firadenovec-vncg; Adstiladrin) is a non-replicating adenoviral vector-based gene therapy developed by Ferring Pharmaceuticals for the treatment of high-risk Bacillus Calmette-Guérin (BCG)-unresponsive non-muscle invasive bladder cancer (NMIBC). Nadofaragene firadenovec constitutes vector DNA that encodes for interferon (IFN)-α2b and is the first approved gene therapy in bladder cancer. The production of IFN-α2b by transfected urothelial cells is associated with anticancer activity, including immunostimulatory, antiangiogenic and apoptotic effects. In December 2022, nadofaragene firadenovec received its first global approval in the USA for the treatment of high-risk BCG-unresponsive NMIBC with carcinoma in situ (CIS) with or without papillary tumours in adults. This article summarizes the milestones in the development of nadofaragene firadenovec leading to this first approval for this indication.

摘要

纳武拉基因 firadenovec(纳武拉基因 firadenovec-vncg;Adstiladrin)是费森尤斯卡比公司开发的一种非复制型腺病毒载体基因治疗药物,用于治疗高危卡介苗(BCG)无应答性非肌肉浸润性膀胱癌(NMIBC)。纳武拉基因 firadenovec 由编码干扰素(IFN)-α2b 的载体 DNA 组成,是首个获批用于膀胱癌的基因治疗药物。转染的尿路上皮细胞产生 IFN-α2b 与抗癌活性相关,包括免疫刺激、抗血管生成和凋亡作用。2022 年 12 月,纳武拉基因 firadenovec 在美国获得首次全球批准,用于治疗高危卡介苗无应答性非肌肉浸润性膀胱癌伴原位癌(CIS)伴或不伴乳头状肿瘤的成人患者。本文总结了纳武拉基因 firadenovec 研发过程中的重要里程碑事件,这些事件促成了该药在该适应证的首次批准。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ed5/10239371/5db0f0d98594/40265_2023_1846_Figa_HTML.jpg

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