Progression of Ebola Therapeutics During the 2014-2015 Outbreak

被引:52
作者
Mendoza, Emelissa J. [1 ,2 ]
Qiu, Xiangguo [1 ,3 ]
Kobinger, Gary P. [1 ,2 ,3 ,4 ]
机构
[1] Publ Hlth Agcy Canada, Natl Microbiol Lab, Special Pathogens Program, Winnipeg, MB, Canada
[2] Univ Manitoba, Dept Immunol, Winnipeg, MB, Canada
[3] Univ Manitoba, Dept Med Microbiol, Winnipeg, MB, Canada
[4] Univ Penn, Sch Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
基金
加拿大健康研究院;
关键词
VIRUS DISEASE; CONVALESCENT PLASMA; HEMORRHAGIC-FEVER; NONHUMAN-PRIMATES; PATIENT; FAVIPIRAVIR; AMIODARONE; GLYCOPROTEIN; INFECTION; FAILURE;
D O I
10.1016/j.molmed.2015.12.005
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 recent Ebola virus (EBOV) outbreak in West Africa was the deadliest EBOV epidemic in history, highlighting the need for a safe and efficacious treatment against EBOV disease (EVD). In the absence of an approved treatment, experimental drugs were utilized under compassionate grounds hoping to diminish EVD-associated morbidity and mortality. As more data were collected from safety studies, Phase II/III clinical trials were introduced in Guinea, Sierra Leone, and Liberia to test promising candidates, including small-molecule drugs, RNA based treatments, and antibody-based therapies. In this review, we summarize the use of, and preliminary observations from, current clinical trials with EVD therapeutics, shedding light on experimental drug selection, emergency clinical evaluation, and the impact these factors may have on future infectious disease outbreaks.
引用
收藏
页码:164 / 173
页数:10
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