2019年冠状病毒病(COVID-19)
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
效力
病毒学
体内
爆发
大流行
药理学
冠状病毒
临床试验
体外
蛋白酶抑制剂(药理学)
生物
医学
病毒
化学
病毒载量
传染病(医学专业)
内科学
疾病
生物技术
抗逆转录病毒疗法
生物化学
作者
Dafydd R. Owen,Charlotte Allerton,Annaliesa S. Anderson,Lisa Aschenbrenner,Melissa Avery,Simon Berritt,Britton Boras,Rhonda D. Cardin,Anthony Carlo,Karen J. Coffman,Alyssa Dantonio,Li Di,Heather Eng,Rose Ann Ferre,K.S. Gajiwala,Scott Gibson,S.E. Greasley,Brett L. Hurst,Eugene P. Kadar,Amit S. Kalgutkar
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2021-11-02
卷期号:374 (6575): 1586-1593
被引量:1537
标识
DOI:10.1126/science.abl4784
摘要
The worldwide outbreak of COVID-19 caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has become a global pandemic. Alongside vaccines, antiviral therapeutics are an important part of the healthcare response to countering the ongoing threat presented by COVID-19. Here, we report the discovery and characterization of PF-07321332, an orally bioavailable SARS-CoV-2 main protease inhibitor with in vitro pan-human coronavirus antiviral activity and excellent off-target selectivity and in vivo safety profiles. PF-07321332 has demonstrated oral activity in a mouse-adapted SARS-CoV-2 model and has achieved oral plasma concentrations exceeding the in vitro antiviral cell potency in a phase 1 clinical trial in healthy human participants.
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