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Ebanga™: The most recent FDA-approved drug for treating Ebola

Affiliation
Department of Microbiology ,School of Medicine ,Tehran University of Medical Sciences ,Tehran ,Iran
Taki, Elahe;
Affiliation
Behbahan Faculty of Medical Sciences ,Behbahan ,Iran
Ghanavati, Roya;
Affiliation
Department of Basic Sciences ,Shoushtar Faculty of Medical Sciences ,Shoushtar ,Iran
Navidifar, Tahereh;
Affiliation
Department of Microbiology ,School of Medicine ,Iran University of Medical Sciences ,Tehran ,Iran
Dashtbin, Shirin;
Affiliation
Department of Laboratory Sciences ,School of Paramedical Sciences ,Sabzevar University of Medical Sciences ,Sabzevar ,Iran
Heidary, Mohsen;
Affiliation
Department of Clinical Pharmacy ,School of Pharmacy ,Tehran University of Medical Sciences ,Tehran ,Iran
Moghadamnia, Marjan

Ebolavirus (EBOV) is a virulent pathogen that causes Ebola virus disease (EVD), which is a life-threatening human condition with a fatality rate of up to 90%. Since the first outbreak in Africa in 1976, several outbreaks and epidemics of EBOV have occurred across the globe. While EVD is recognized as a serious threat to human health and outbreaks occur almost every year, the treatment options for the disease are limited. In designing therapeutic strategies against EBOV infection, viral structural proteins, such as glycoprotein (GP), could be an excellent target for neutralizing the virus. According to the latest research, GP-specific antibodies are the most efficient post-exposure treatments for EVD. Ansuvimab-zykl, i.e., mAb114 (Ebanga™), is a recent FDA-approved human immunoglobulin monoclonal antibody targeting EBOV GP. This review provides a brief overview of the pharmacological effects and safety profile of ansuvimab in clinical trials and provides insights into the precise mechanism of this new drug for treating EVD.

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License Holder: Copyright © 2023 Taki, Ghanavati, Navidifar, Dashtbin, Heidary and Moghadamnia.

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