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Challenges and Opportunities in Developing Respiratory Syncytial Virus Therapeutics

Two meetings, one sponsored by the Wellcome Trust in 2012 and the other by the Global Virology Foundation in 2013, assembled academic, public health and pharmaceutical industry experts to assess the challenges and opportunities for developing antivirals for the treatment of respiratory syncytial vir...

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Autores principales: Simões, Eric A. F., DeVincenzo, John P., Boeckh, Michael, Bont, Louis, Crowe, James E., Griffiths, Paul, Hayden, Frederick G., Hodinka, Richard L., Smyth, Rosalind L., Spencer, Keith, Thirstrup, Steffen, Walsh, Edward E., Whitley, Richard J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4345819/
https://www.ncbi.nlm.nih.gov/pubmed/25713060
http://dx.doi.org/10.1093/infdis/jiu828
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author Simões, Eric A. F.
DeVincenzo, John P.
Boeckh, Michael
Bont, Louis
Crowe, James E.
Griffiths, Paul
Hayden, Frederick G.
Hodinka, Richard L.
Smyth, Rosalind L.
Spencer, Keith
Thirstrup, Steffen
Walsh, Edward E.
Whitley, Richard J.
author_facet Simões, Eric A. F.
DeVincenzo, John P.
Boeckh, Michael
Bont, Louis
Crowe, James E.
Griffiths, Paul
Hayden, Frederick G.
Hodinka, Richard L.
Smyth, Rosalind L.
Spencer, Keith
Thirstrup, Steffen
Walsh, Edward E.
Whitley, Richard J.
author_sort Simões, Eric A. F.
collection PubMed
description Two meetings, one sponsored by the Wellcome Trust in 2012 and the other by the Global Virology Foundation in 2013, assembled academic, public health and pharmaceutical industry experts to assess the challenges and opportunities for developing antivirals for the treatment of respiratory syncytial virus (RSV) infections. The practicalities of clinical trials and establishing reliable outcome measures in different target groups were discussed in the context of the regulatory pathways that could accelerate the translation of promising compounds into licensed agents. RSV drug development is hampered by the perceptions of a relatively small and fragmented market that may discourage major pharmaceutical company investment. Conversely, the public health need is far too large for RSV to be designated an orphan or neglected disease. Recent advances in understanding RSV epidemiology, improved point-of-care diagnostics, and identification of candidate antiviral drugs argue that the major obstacles to drug development can and will be overcome. Further progress will depend on studies of disease pathogenesis and knowledge provided from controlled clinical trials of these new therapeutic agents. The use of combinations of inhibitors that have different mechanisms of action may be necessary to increase antiviral potency and reduce the risk of resistance emergence.
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spelling pubmed-43458192015-03-17 Challenges and Opportunities in Developing Respiratory Syncytial Virus Therapeutics Simões, Eric A. F. DeVincenzo, John P. Boeckh, Michael Bont, Louis Crowe, James E. Griffiths, Paul Hayden, Frederick G. Hodinka, Richard L. Smyth, Rosalind L. Spencer, Keith Thirstrup, Steffen Walsh, Edward E. Whitley, Richard J. J Infect Dis Supplement Article Two meetings, one sponsored by the Wellcome Trust in 2012 and the other by the Global Virology Foundation in 2013, assembled academic, public health and pharmaceutical industry experts to assess the challenges and opportunities for developing antivirals for the treatment of respiratory syncytial virus (RSV) infections. The practicalities of clinical trials and establishing reliable outcome measures in different target groups were discussed in the context of the regulatory pathways that could accelerate the translation of promising compounds into licensed agents. RSV drug development is hampered by the perceptions of a relatively small and fragmented market that may discourage major pharmaceutical company investment. Conversely, the public health need is far too large for RSV to be designated an orphan or neglected disease. Recent advances in understanding RSV epidemiology, improved point-of-care diagnostics, and identification of candidate antiviral drugs argue that the major obstacles to drug development can and will be overcome. Further progress will depend on studies of disease pathogenesis and knowledge provided from controlled clinical trials of these new therapeutic agents. The use of combinations of inhibitors that have different mechanisms of action may be necessary to increase antiviral potency and reduce the risk of resistance emergence. Oxford University Press 2015-03-15 2015-02-23 /pmc/articles/PMC4345819/ /pubmed/25713060 http://dx.doi.org/10.1093/infdis/jiu828 Text en © The Author 2015. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Supplement Article
Simões, Eric A. F.
DeVincenzo, John P.
Boeckh, Michael
Bont, Louis
Crowe, James E.
Griffiths, Paul
Hayden, Frederick G.
Hodinka, Richard L.
Smyth, Rosalind L.
Spencer, Keith
Thirstrup, Steffen
Walsh, Edward E.
Whitley, Richard J.
Challenges and Opportunities in Developing Respiratory Syncytial Virus Therapeutics
title Challenges and Opportunities in Developing Respiratory Syncytial Virus Therapeutics
title_full Challenges and Opportunities in Developing Respiratory Syncytial Virus Therapeutics
title_fullStr Challenges and Opportunities in Developing Respiratory Syncytial Virus Therapeutics
title_full_unstemmed Challenges and Opportunities in Developing Respiratory Syncytial Virus Therapeutics
title_short Challenges and Opportunities in Developing Respiratory Syncytial Virus Therapeutics
title_sort challenges and opportunities in developing respiratory syncytial virus therapeutics
topic Supplement Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4345819/
https://www.ncbi.nlm.nih.gov/pubmed/25713060
http://dx.doi.org/10.1093/infdis/jiu828
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