Favipiravir: Pharmacokinetics and Concerns About Clinical Trials for 2019-nCoV Infection

被引:291
作者
Du Yin-Xiao [1 ,2 ,3 ]
Chen Xiao-Ping [1 ,2 ,3 ]
机构
[1] Cent South Univ, Xiangya Hosp, Dept Clin Pharmacol, Changsha, Hunan, Peoples R China
[2] Cent South Univ, Inst Clin Pharmacol, Hunan Key Lab Pharmacogenet, Changsha, Hunan, Peoples R China
[3] Cent South Univ, Xiangya Hosp, Natl Clin Res Ctr Geriatr Disorders, Changsha, Hunan, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
HUMAN LIVER; ALDEHYDE OXIDASE; IN-VITRO; INHIBITION; METABOLISM; ZALEPLON; T-705;
D O I
10.1002/cpt.1844
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
An outbreak of 2019-nCoV infection in China has spread across the world. No specific antiviral drugs have been approved for the treatment of COVID-2019. In addition to the recommended antiviral drugs, such as interferon-& x251;, lopinavir/ritonavir, ribavirin, and chloroquine phosphate, some clinical trials focusing on virus RNA-dependent RNA polymerase (RdRp) inhibitors have been registered and initiated. Favipiravir, a purine nucleic acid analog and potent RdRp inhibitor approved for use in influenza, is also considered in several clinical trials. Herein, we summarized the pharmacokinetic characteristics of favipiravir and possible drug-drug interactions from the view of drug metabolism. We hope this will be helpful for the design of clinical trials for favipiravir in COVID-2019, as data regarding in vitro virus inhibition and efficacy in preclinical animal studies are still not available.
引用
收藏
页码:242 / 247
页数:6
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