An Update on SARS-CoV-2 Clinical Trial Results-What We Can Learn for the Next Pandemic

被引:5
|
作者
Arman, Benediktus Yohan [1 ,2 ]
Brun, Juliane [1 ,2 ]
Hill, Michelle L. [3 ]
Zitzmann, Nicole [1 ,2 ]
von Delft, Annette [2 ,4 ]
Gavriilaki, Eleni
机构
[1] Univ Oxford, Oxford Glycobiol Inst, Dept Biochem, Antiviral Drug Discovery Unit, Oxford OX1 3QU, England
[2] Univ Oxford, Kavli Inst Nanosci Discovery, Oxford OX1 3QU, England
[3] Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 3RE, England
[4] Univ Oxford, Ctr Med Discovery, Nuffield Dept Med, Oxford OX3 7BN, England
关键词
COVID-19; SARS-CoV-2; coronavirus; therapeutics; clinical trial; drug discovery; RANDOMIZED CONTROLLED-TRIAL; TO-MODERATE COVID-19; OPEN-LABEL; DOUBLE-BLIND; HOSPITALIZED-PATIENTS; RNA-POLYMERASE; LOPINAVIR-RITONAVIR; INTERFERON BETA-1B; DRUG DISCOVERY; EFFICACY;
D O I
10.3390/ijms25010354
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The coronavirus disease 2019 (COVID-19) pandemic has claimed over 7 million lives worldwide, providing a stark reminder of the importance of pandemic preparedness. Due to the lack of approved antiviral drugs effective against coronaviruses at the start of the pandemic, the world largely relied on repurposed efforts. Here, we summarise results from randomised controlled trials to date, as well as selected in vitro data of directly acting antivirals, host-targeting antivirals, and immunomodulatory drugs. Overall, repurposing efforts evaluating directly acting antivirals targeting other viral families were largely unsuccessful, whereas several immunomodulatory drugs led to clinical improvement in hospitalised patients with severe disease. In addition, accelerated drug discovery efforts during the pandemic progressed to multiple novel directly acting antivirals with clinical efficacy, including small molecule inhibitors and monoclonal antibodies. We argue that large-scale investment is required to prepare for future pandemics; both to develop an arsenal of broad-spectrum antivirals beyond coronaviruses and build worldwide clinical trial networks that can be rapidly utilised.
引用
收藏
页数:42
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