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Clinical potential of brodalumab in the management of psoriasis: the evidence to date

Brodalumab is an anti-IL-17 receptor monoclonal antibody currently in development for the treatment of moderate-to-severe plaque psoriasis. With many systemic psoriasis therapies to choose from, and several newer agents in development, physicians need up to date evidence for the use of these drugs....

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Autores principales: Sandoval, Laura F, Williams, Brooke, Feldman, Steven R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5683110/
https://www.ncbi.nlm.nih.gov/pubmed/29387580
http://dx.doi.org/10.2147/PTT.S49996
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author Sandoval, Laura F
Williams, Brooke
Feldman, Steven R
author_facet Sandoval, Laura F
Williams, Brooke
Feldman, Steven R
author_sort Sandoval, Laura F
collection PubMed
description Brodalumab is an anti-IL-17 receptor monoclonal antibody currently in development for the treatment of moderate-to-severe plaque psoriasis. With many systemic psoriasis therapies to choose from, and several newer agents in development, physicians need up to date evidence for the use of these drugs. A PubMed search was conducted through August 1, 2014 to identify randomized controlled trials and systematic reviews of brodalumab for the treatment of psoriasis. Results of Phase I and II trials, as well as a few smaller studies, have provided promising data on efficacy, safety, health-related quality of life, pharmacokinetics, and changes in lesional skin. Early Phase III data continue to support the use of brodalumab as a potentially valuable option for the treatment of psoriasis.
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spelling pubmed-56831102018-01-31 Clinical potential of brodalumab in the management of psoriasis: the evidence to date Sandoval, Laura F Williams, Brooke Feldman, Steven R Psoriasis (Auckl) Review Brodalumab is an anti-IL-17 receptor monoclonal antibody currently in development for the treatment of moderate-to-severe plaque psoriasis. With many systemic psoriasis therapies to choose from, and several newer agents in development, physicians need up to date evidence for the use of these drugs. A PubMed search was conducted through August 1, 2014 to identify randomized controlled trials and systematic reviews of brodalumab for the treatment of psoriasis. Results of Phase I and II trials, as well as a few smaller studies, have provided promising data on efficacy, safety, health-related quality of life, pharmacokinetics, and changes in lesional skin. Early Phase III data continue to support the use of brodalumab as a potentially valuable option for the treatment of psoriasis. Dove Medical Press 2015-03-11 /pmc/articles/PMC5683110/ /pubmed/29387580 http://dx.doi.org/10.2147/PTT.S49996 Text en © 2015 Sandoval et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Sandoval, Laura F
Williams, Brooke
Feldman, Steven R
Clinical potential of brodalumab in the management of psoriasis: the evidence to date
title Clinical potential of brodalumab in the management of psoriasis: the evidence to date
title_full Clinical potential of brodalumab in the management of psoriasis: the evidence to date
title_fullStr Clinical potential of brodalumab in the management of psoriasis: the evidence to date
title_full_unstemmed Clinical potential of brodalumab in the management of psoriasis: the evidence to date
title_short Clinical potential of brodalumab in the management of psoriasis: the evidence to date
title_sort clinical potential of brodalumab in the management of psoriasis: the evidence to date
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5683110/
https://www.ncbi.nlm.nih.gov/pubmed/29387580
http://dx.doi.org/10.2147/PTT.S49996
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