Suppr超能文献

帕替沙那:全球首次获批。

Patisiran: First Global Approval.

机构信息

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

出版信息

Drugs. 2018 Oct;78(15):1625-1631. doi: 10.1007/s40265-018-0983-6.

Abstract

Patisiran (ONPATTRO™) is a double-stranded small interfering RNA encapsulated in a lipid nanoparticle for delivery to hepatocytes. By specifically binding to a genetically conserved sequence in the 3' untranslated region of mutant and wild-type transthyretin (TTR) messenger RNA, patisiran causes its degradation (via RNA interference) and subsequently a reduction in serum TTR protein levels and tissue TTR protein deposits. Patisiran has been developed by Alnylam Pharmaceuticals; it was recently approved in the USA for the treatment of the polyneuropathy of hereditary TTR-mediated amyloidosis (hATTR) in adults and subsequently approved in the EU for the treatment of hATTR in adults with stage 1 or 2 polyneuropathy. The recommended dosage, administered as a single intravenous infusion over approximately 80 min, is 0.3 mg/kg once every 3 weeks for patients weighing < 100 kg and 30 mg once every 3 weeks for patients weighing ≥ 100 kg. This article summarizes the milestones in the development of patisiran leading to these approvals.

摘要

帕替沙那(ONPATTRO™)是一种双链小干扰 RNA,封装在脂质纳米颗粒中,用于递送至肝细胞。通过与突变型和野生型转甲状腺素蛋白 (TTR) 信使 RNA 的 3'非翻译区中具有遗传保守性的序列特异性结合,帕替沙那导致其降解(通过 RNA 干扰),随后血清 TTR 蛋白水平和组织 TTR 蛋白沉积减少。帕替沙那由 Alnylam 制药公司开发;它最近在美国获得批准,用于治疗成人遗传性 TTR 介导的淀粉样变性(hATTR)的多发性神经病,随后在欧盟获得批准,用于治疗成人 1 期或 2 期多发性神经病的 hATTR。推荐剂量为 30mg,每 3 周一次,用于体重≥100kg 的患者;对于体重<100kg 的患者,剂量为 0.3mg/kg,每 3 周一次。本文总结了导致这些批准的帕替沙那开发过程中的重要里程碑。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验