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REGN-EB3: First Approval
REGN-EB3 (INMAZEB(®), Regeneron Pharmaceuticals) is a combination of three fully-human monoclonal antibodies—atoltivimab (REGN3470), maftivimab (REGN3479), and odesivimab (REGN3471) —that target Ebola virus glycoprotein. Based on the results of the PALM study conducted during an Ebola outbreak in th...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer International Publishing
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7799152/ https://www.ncbi.nlm.nih.gov/pubmed/33432551 http://dx.doi.org/10.1007/s40265-020-01452-3 |
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author | Markham, Anthony |
author_facet | Markham, Anthony |
author_sort | Markham, Anthony |
collection | PubMed |
description | REGN-EB3 (INMAZEB(®), Regeneron Pharmaceuticals) is a combination of three fully-human monoclonal antibodies—atoltivimab (REGN3470), maftivimab (REGN3479), and odesivimab (REGN3471) —that target Ebola virus glycoprotein. Based on the results of the PALM study conducted during an Ebola outbreak in the Democratic Republic of Congo, REGN-EB3 was recently approved by the US FDA as a treatment for Ebola virus infection. This article summarizes the milestones in the development of REGN-EB3 leading to this first approval for the treatment of infection caused by Zaire ebolavirus (Ebola virus) in adult and paediatric patients. |
format | Online Article Text |
id | pubmed-7799152 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-77991522021-01-12 REGN-EB3: First Approval Markham, Anthony Drugs AdisInsight Report REGN-EB3 (INMAZEB(®), Regeneron Pharmaceuticals) is a combination of three fully-human monoclonal antibodies—atoltivimab (REGN3470), maftivimab (REGN3479), and odesivimab (REGN3471) —that target Ebola virus glycoprotein. Based on the results of the PALM study conducted during an Ebola outbreak in the Democratic Republic of Congo, REGN-EB3 was recently approved by the US FDA as a treatment for Ebola virus infection. This article summarizes the milestones in the development of REGN-EB3 leading to this first approval for the treatment of infection caused by Zaire ebolavirus (Ebola virus) in adult and paediatric patients. Springer International Publishing 2021-01-11 2021 /pmc/articles/PMC7799152/ /pubmed/33432551 http://dx.doi.org/10.1007/s40265-020-01452-3 Text en © Springer Nature Switzerland AG 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | AdisInsight Report Markham, Anthony REGN-EB3: First Approval |
title | REGN-EB3: First Approval |
title_full | REGN-EB3: First Approval |
title_fullStr | REGN-EB3: First Approval |
title_full_unstemmed | REGN-EB3: First Approval |
title_short | REGN-EB3: First Approval |
title_sort | regn-eb3: first approval |
topic | AdisInsight Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7799152/ https://www.ncbi.nlm.nih.gov/pubmed/33432551 http://dx.doi.org/10.1007/s40265-020-01452-3 |
work_keys_str_mv | AT markhamanthony regneb3firstapproval |