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What’s New in Topicals for Atopic Dermatitis?
Atopic dermatitis (AD) is a chronic inflammatory skin condition that can have tremendous impact on quality of life for affected children and adults. First-line therapy for acute management of AD includes topical therapies such as corticosteroids, calcineurin inhibitors, and, more recently, the phosp...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9464760/ https://www.ncbi.nlm.nih.gov/pubmed/36048410 http://dx.doi.org/10.1007/s40257-022-00712-0 |
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author | Kleinman, Elana Laborada, Jennifer Metterle, Lauren Eichenfield, Lawrence F. |
author_facet | Kleinman, Elana Laborada, Jennifer Metterle, Lauren Eichenfield, Lawrence F. |
author_sort | Kleinman, Elana |
collection | PubMed |
description | Atopic dermatitis (AD) is a chronic inflammatory skin condition that can have tremendous impact on quality of life for affected children and adults. First-line therapy for acute management of AD includes topical therapies such as corticosteroids, calcineurin inhibitors, and, more recently, the phosphodiesterase inhibitor crisaborole. Topical agents have remained the mainstay therapy for decades; however, there has been a longstanding need for topical therapies with high efficacy and low risk of adverse effects with long-term use. Given the ongoing advances in understanding the pathogenesis of AD, there are novel targets for pharmacological intervention. We are now in an unprecedented time with more than 40 topical treatments in the pipeline for AD in addition to many developments and treatments on the horizon. This review summarizes selected therapeutic topical agents in later phases of development that target various aspects in the pathogenesis of AD such as Janus kinase inhibition (ruxolitinib and delgocitinib), phosphodiesterase-4 inhibition (roflumilast and difamilast), aryl hydrocarbon modulation (tapinarof), and modulation of the microbiome. We also review novel targeted therapies that are in early phase clinical trials, including AMTX-100, BEN-2293, and PRN473. Preliminary findings on efficacy and tolerability of most of these agents are promising, but further studies are warranted to evaluate the long-term safety and efficacy of these novel agents against the current standard of care. |
format | Online Article Text |
id | pubmed-9464760 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-94647602022-09-13 What’s New in Topicals for Atopic Dermatitis? Kleinman, Elana Laborada, Jennifer Metterle, Lauren Eichenfield, Lawrence F. Am J Clin Dermatol Leading Article Atopic dermatitis (AD) is a chronic inflammatory skin condition that can have tremendous impact on quality of life for affected children and adults. First-line therapy for acute management of AD includes topical therapies such as corticosteroids, calcineurin inhibitors, and, more recently, the phosphodiesterase inhibitor crisaborole. Topical agents have remained the mainstay therapy for decades; however, there has been a longstanding need for topical therapies with high efficacy and low risk of adverse effects with long-term use. Given the ongoing advances in understanding the pathogenesis of AD, there are novel targets for pharmacological intervention. We are now in an unprecedented time with more than 40 topical treatments in the pipeline for AD in addition to many developments and treatments on the horizon. This review summarizes selected therapeutic topical agents in later phases of development that target various aspects in the pathogenesis of AD such as Janus kinase inhibition (ruxolitinib and delgocitinib), phosphodiesterase-4 inhibition (roflumilast and difamilast), aryl hydrocarbon modulation (tapinarof), and modulation of the microbiome. We also review novel targeted therapies that are in early phase clinical trials, including AMTX-100, BEN-2293, and PRN473. Preliminary findings on efficacy and tolerability of most of these agents are promising, but further studies are warranted to evaluate the long-term safety and efficacy of these novel agents against the current standard of care. Springer International Publishing 2022-09-01 2022 /pmc/articles/PMC9464760/ /pubmed/36048410 http://dx.doi.org/10.1007/s40257-022-00712-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Leading Article Kleinman, Elana Laborada, Jennifer Metterle, Lauren Eichenfield, Lawrence F. What’s New in Topicals for Atopic Dermatitis? |
title | What’s New in Topicals for Atopic Dermatitis? |
title_full | What’s New in Topicals for Atopic Dermatitis? |
title_fullStr | What’s New in Topicals for Atopic Dermatitis? |
title_full_unstemmed | What’s New in Topicals for Atopic Dermatitis? |
title_short | What’s New in Topicals for Atopic Dermatitis? |
title_sort | what’s new in topicals for atopic dermatitis? |
topic | Leading Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9464760/ https://www.ncbi.nlm.nih.gov/pubmed/36048410 http://dx.doi.org/10.1007/s40257-022-00712-0 |
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