Cargando…

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

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 a...

Descripción completa

Detalles Bibliográficos
Autores principales: Taki, Elahe, Ghanavati, Roya, Navidifar, Tahereh, Dashtbin, Shirin, Heidary, Mohsen, Moghadamnia, Marjan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032372/
https://www.ncbi.nlm.nih.gov/pubmed/36969842
http://dx.doi.org/10.3389/fphar.2023.1083429
_version_ 1784910785208647680
author Taki, Elahe
Ghanavati, Roya
Navidifar, Tahereh
Dashtbin, Shirin
Heidary, Mohsen
Moghadamnia, Marjan
author_facet Taki, Elahe
Ghanavati, Roya
Navidifar, Tahereh
Dashtbin, Shirin
Heidary, Mohsen
Moghadamnia, Marjan
author_sort Taki, Elahe
collection PubMed
description 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.
format Online
Article
Text
id pubmed-10032372
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-100323722023-03-23 Ebanga™: The most recent FDA-approved drug for treating Ebola Taki, Elahe Ghanavati, Roya Navidifar, Tahereh Dashtbin, Shirin Heidary, Mohsen Moghadamnia, Marjan Front Pharmacol Pharmacology 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. Frontiers Media S.A. 2023-03-08 /pmc/articles/PMC10032372/ /pubmed/36969842 http://dx.doi.org/10.3389/fphar.2023.1083429 Text en Copyright © 2023 Taki, Ghanavati, Navidifar, Dashtbin, Heidary and Moghadamnia. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Taki, Elahe
Ghanavati, Roya
Navidifar, Tahereh
Dashtbin, Shirin
Heidary, Mohsen
Moghadamnia, Marjan
Ebanga™: The most recent FDA-approved drug for treating Ebola
title Ebanga™: The most recent FDA-approved drug for treating Ebola
title_full Ebanga™: The most recent FDA-approved drug for treating Ebola
title_fullStr Ebanga™: The most recent FDA-approved drug for treating Ebola
title_full_unstemmed Ebanga™: The most recent FDA-approved drug for treating Ebola
title_short Ebanga™: The most recent FDA-approved drug for treating Ebola
title_sort ebanga™: the most recent fda-approved drug for treating ebola
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032372/
https://www.ncbi.nlm.nih.gov/pubmed/36969842
http://dx.doi.org/10.3389/fphar.2023.1083429
work_keys_str_mv AT takielahe ebangathemostrecentfdaapproveddrugfortreatingebola
AT ghanavatiroya ebangathemostrecentfdaapproveddrugfortreatingebola
AT navidifartahereh ebangathemostrecentfdaapproveddrugfortreatingebola
AT dashtbinshirin ebangathemostrecentfdaapproveddrugfortreatingebola
AT heidarymohsen ebangathemostrecentfdaapproveddrugfortreatingebola
AT moghadamniamarjan ebangathemostrecentfdaapproveddrugfortreatingebola