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Recent highlights in the development of new antiviral drugs

Twenty antiviral drugs, that is about half of those that are currently approved, are formally licensed for clinical use in the treatment of human immunodeficiency virus infections (acquired immune deficiency syndrome). The others are used in the treatment of herpesvirus (e.g. herpes simplex virus, v...

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Autor principal: De Clercq, Erik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7108330/
https://www.ncbi.nlm.nih.gov/pubmed/16125443
http://dx.doi.org/10.1016/j.mib.2005.08.010
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author De Clercq, Erik
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description Twenty antiviral drugs, that is about half of those that are currently approved, are formally licensed for clinical use in the treatment of human immunodeficiency virus infections (acquired immune deficiency syndrome). The others are used in the treatment of herpesvirus (e.g. herpes simplex virus, varicella zoster virus and cytomegalo virus), hepatitis B virus, hepatitis C virus or influenza virus infections. Recent endeavours have focussed on the development of improved antiviral therapies for virus infections that have already proved amenable to antiviral drug treatment, as well as for virus infections for which, at present, no antiviral drugs have been formally approved (i.e. human papilloma viruses, adenoviruses, human herpesvirus type 6, poxviruses, severe acute respiratory syndrome coronavirus and hemorrhagic fever viruses).
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spelling pubmed-71083302020-03-31 Recent highlights in the development of new antiviral drugs De Clercq, Erik Curr Opin Microbiol Article Twenty antiviral drugs, that is about half of those that are currently approved, are formally licensed for clinical use in the treatment of human immunodeficiency virus infections (acquired immune deficiency syndrome). The others are used in the treatment of herpesvirus (e.g. herpes simplex virus, varicella zoster virus and cytomegalo virus), hepatitis B virus, hepatitis C virus or influenza virus infections. Recent endeavours have focussed on the development of improved antiviral therapies for virus infections that have already proved amenable to antiviral drug treatment, as well as for virus infections for which, at present, no antiviral drugs have been formally approved (i.e. human papilloma viruses, adenoviruses, human herpesvirus type 6, poxviruses, severe acute respiratory syndrome coronavirus and hemorrhagic fever viruses). Elsevier Ltd. 2005-10 2005-08-24 /pmc/articles/PMC7108330/ /pubmed/16125443 http://dx.doi.org/10.1016/j.mib.2005.08.010 Text en Copyright © 2005 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
De Clercq, Erik
Recent highlights in the development of new antiviral drugs
title Recent highlights in the development of new antiviral drugs
title_full Recent highlights in the development of new antiviral drugs
title_fullStr Recent highlights in the development of new antiviral drugs
title_full_unstemmed Recent highlights in the development of new antiviral drugs
title_short Recent highlights in the development of new antiviral drugs
title_sort recent highlights in the development of new antiviral drugs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7108330/
https://www.ncbi.nlm.nih.gov/pubmed/16125443
http://dx.doi.org/10.1016/j.mib.2005.08.010
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