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10亿美元收购RNA干扰疗法ARO-AAT,治疗遗传性肝病

2020-10-11 MedSci原创 MedSci原创

ARO-AAT作为一种RNA干扰(RNAi)疗法,通过抑制突变型α-1抗胰蛋白酶(致病因子)的表达发挥作用。

Arrowhead与武田达成了一项十亿美元的重大协议,武田将支付3亿美元的预付款和高达7.4亿美元的里程碑付款,以共同开发ARO-AAT治疗α-1抗胰蛋白酶缺乏性肝病(AATLD)。AATLD是儿童最常见的遗传性肝病。

News - Alpha-1 Foundation

ARO-AAT作为一种RNA干扰(RNAi)疗法,通过降低突变型α-1抗胰蛋白酶(AAT,AATLD的致病因子)的含量发挥作用,目前处于2期临床开发阶段。

图片来源:https://ir.arrowheadpharma.com/static-files/1958847b-495f-4acd-bc27-2f457e33d1ba

武田胃肠病学负责人Asit Parikh博士表示:“AATLD是一种破坏性疾病,目前尚无批准的疗法。ARO-AAT具有从根本上解决AATLD的潜力,可以帮助患者避免肝移植手术及相关合并症的发生。”

武田将获得ARO-AAT在美国以外的独家销售权,而Arrowhead则可在其净销售额中获得20%至25%的分级特许权使用费。

原始出处:

https://www.europeanpharmaceuticalreview.com/news/129967/trial-testing-anti-coronavirus-hivig-plus-remdesivir-in-covid-19-patients/

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    2020-10-11 opzoro

    知识就是财富

    0

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