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

被引:292
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
国家重点研发计划; 中国国家自然科学基金;
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
相关论文
共 29 条
[1]   Clinical and Virological Characteristics of Ebola Virus Disease Patients Treated With Favipiravir (T-705)-Sierra Leone, 2014 [J].
Bai, Chang-Qing ;
Mu, Jin-Song ;
Kargbo, David ;
Song, Ya-Bin ;
Niu, Wen-Kai ;
Nie, Wei-Min ;
Kanu, Alex ;
Liu, Wei-Wei ;
Wang, Yao-Ping ;
Dafae, Foday ;
Yan, Tao ;
Hu, Yi ;
Deng, Yong-Qiang ;
Lu, Hui-Jun ;
Yang, Fan ;
Zhang, Xiao-Guang ;
Sun, Yang ;
Cao, Yu-Xi ;
Su, Hao-Xiang ;
Sun, Yu ;
Liu, Wen-Sen ;
Wang, Cheng-Yu ;
Qian, Jun ;
Liu, Liu ;
Wang, Hong ;
Tong, Yi-Gang ;
Liu, Ze-Yuan ;
Chen, Yun-Song ;
Wang, Hong-Quan ;
Kargbo, Brima ;
Gao, George F. ;
Jiang, Jia-Fu .
CLINICAL INFECTIOUS DISEASES, 2016, 63 (10) :1288-1294
[2]   Synthesis of [18F]Favipiravir and Biodistribution in C3H/HeN Mice as Assessed by Positron Emission Tomography [J].
Bocan, Thomas M. ;
Basuli, Falguni ;
Stafford, Robert G. ;
Brown, Jennifer L. ;
Zhang, Xiang ;
Duplantier, Allen J. ;
Swenson, Rolf E. .
SCIENTIFIC REPORTS, 2019, 9 (1)
[3]  
Cai Q., Engineering
[4]  
Chen C, 2020, FAVIPIRAVIR VERSUS A, DOI DOI 10.1101/2020.03.17.20037432
[5]  
CLARKE SE, 1995, DRUG METAB DISPOS, V23, P251
[6]   Aldehyde oxidase and its role as a drug metabolizing enzyme [J].
Dalvie, Deepak ;
Di, Li .
PHARMACOLOGY & THERAPEUTICS, 2019, 201 :137-180
[7]   Discovering drugs to treat coronavirus disease 2019 (COVID-19) [J].
Dong, Liying ;
Hu, Shasha ;
Gao, Jianjun .
DRUG DISCOVERIES AND THERAPEUTICS, 2020, 14 (01) :58-60
[8]   Mechanism of action of T-705 against influenza virus [J].
Furuta, Y ;
Takahashi, K ;
Kuno-Maekawa, M ;
Sangawa, H ;
Uehara, S ;
Kozaki, K ;
Nomura, N ;
Egawa, H ;
Shiraki, K .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (03) :981-986
[9]   Favipiravir (T-705), a broad spectrum inhibitor of viral RNA polymerase [J].
Furuta, Yousuke ;
Komeno, Takashi ;
Nakamura, Takaaki .
PROCEEDINGS OF THE JAPAN ACADEMY SERIES B-PHYSICAL AND BIOLOGICAL SCIENCES, 2017, 93 (07) :449-463
[10]   Metabolism of zaleplon by human liver: evidence for involvement of aldehyde oxidase [J].
Lake, BG ;
Ball, SE ;
Kao, J ;
Renwick, AB ;
Price, RJ ;
Scatina, JA .
XENOBIOTICA, 2002, 32 (10) :835-847