托珠单抗
药物重新定位
大流行
医学
重新调整用途
2019年冠状病毒病(COVID-19)
冠状病毒
临床试验
利托那韦
药物开发
药品
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
药物发现
病毒学
药理学
重症监护医学
传染病(医学专业)
疾病
病毒
生物信息学
病毒载量
生物
内科学
生态学
抗逆转录病毒疗法
作者
Guangdi Li,Rolf Hilgenfeld,Richard J. Whitley,Erik De Clercq
标识
DOI:10.1038/s41573-023-00672-y
摘要
The coronavirus disease 2019 (COVID-19) pandemic has stimulated tremendous efforts to develop therapeutic strategies that target severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and/or human proteins to control viral infection, encompassing hundreds of potential drugs and thousands of patients in clinical trials. So far, a few small-molecule antiviral drugs (nirmatrelvir-ritonavir, remdesivir and molnupiravir) and 11 monoclonal antibodies have been marketed for the treatment of COVID-19, mostly requiring administration within 10 days of symptom onset. In addition, hospitalized patients with severe or critical COVID-19 may benefit from treatment with previously approved immunomodulatory drugs, including glucocorticoids such as dexamethasone, cytokine antagonists such as tocilizumab and Janus kinase inhibitors such as baricitinib. Here, we summarize progress with COVID-19 drug discovery, based on accumulated findings since the pandemic began and a comprehensive list of clinical and preclinical inhibitors with anti-coronavirus activities. We also discuss the lessons learned from COVID-19 and other infectious diseases with regard to drug repurposing strategies, pan-coronavirus drug targets, in vitro assays and animal models, and platform trial design for the development of therapeutics to tackle COVID-19, long COVID and pathogenic coronaviruses in future outbreaks.
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