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Baricitinib: A Review in Moderate to Severe Atopic Dermatitis
Baricitinib (Olumiant(®)) is an oral small molecule inhibitor of Janus kinase (JAK)1 and JAK2, which have been implicated in the pathogenesis of atopic dermatitis (AD). In phase III studies in adults with moderate to severe AD who were inadequately controlled with topical corticosteroids (TCS) or sy...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer International Publishing
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9061224/ https://www.ncbi.nlm.nih.gov/pubmed/35503162 http://dx.doi.org/10.1007/s40257-022-00684-1 |
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author | Hoy, Sheridan M. |
author_facet | Hoy, Sheridan M. |
author_sort | Hoy, Sheridan M. |
collection | PubMed |
description | Baricitinib (Olumiant(®)) is an oral small molecule inhibitor of Janus kinase (JAK)1 and JAK2, which have been implicated in the pathogenesis of atopic dermatitis (AD). In phase III studies in adults with moderate to severe AD who were inadequately controlled with topical corticosteroids (TCS) or systemic treatments (e.g. ciclosporin), or for whom these therapies were not advisable, baricitinib, alone or in combination with TCS, achieved significant and/or clinically relevant improvements in multiple measures of disease severity, pruritus, skin pain, sleep disturbance and health-related quality of life (HR-QOL) over 16 weeks. Benefit onset was rapid, with efficacy generally sustained over the longer term (treatment duration ≤ 68 weeks). In this patient population, the safety profile of baricitinib was consistent with that established in the moderate to severe rheumatoid arthritis (RA) population. Although further longer-term data would be beneficial, current evidence indicates that baricitinib, alone or in combination with TCS, provides an oral alternative to subcutaneous biologics for the treatment of moderate to severe AD in adults who are candidates for systemic therapy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40257-022-00684-1. |
format | Online Article Text |
id | pubmed-9061224 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-90612242022-05-03 Baricitinib: A Review in Moderate to Severe Atopic Dermatitis Hoy, Sheridan M. Am J Clin Dermatol Adis Drug Evaluation Baricitinib (Olumiant(®)) is an oral small molecule inhibitor of Janus kinase (JAK)1 and JAK2, which have been implicated in the pathogenesis of atopic dermatitis (AD). In phase III studies in adults with moderate to severe AD who were inadequately controlled with topical corticosteroids (TCS) or systemic treatments (e.g. ciclosporin), or for whom these therapies were not advisable, baricitinib, alone or in combination with TCS, achieved significant and/or clinically relevant improvements in multiple measures of disease severity, pruritus, skin pain, sleep disturbance and health-related quality of life (HR-QOL) over 16 weeks. Benefit onset was rapid, with efficacy generally sustained over the longer term (treatment duration ≤ 68 weeks). In this patient population, the safety profile of baricitinib was consistent with that established in the moderate to severe rheumatoid arthritis (RA) population. Although further longer-term data would be beneficial, current evidence indicates that baricitinib, alone or in combination with TCS, provides an oral alternative to subcutaneous biologics for the treatment of moderate to severe AD in adults who are candidates for systemic therapy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40257-022-00684-1. Springer International Publishing 2022-05-03 2022 /pmc/articles/PMC9061224/ /pubmed/35503162 http://dx.doi.org/10.1007/s40257-022-00684-1 Text en © Springer Nature 2022, corrected publication 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 | Adis Drug Evaluation Hoy, Sheridan M. Baricitinib: A Review in Moderate to Severe Atopic Dermatitis |
title | Baricitinib: A Review in Moderate to Severe Atopic Dermatitis |
title_full | Baricitinib: A Review in Moderate to Severe Atopic Dermatitis |
title_fullStr | Baricitinib: A Review in Moderate to Severe Atopic Dermatitis |
title_full_unstemmed | Baricitinib: A Review in Moderate to Severe Atopic Dermatitis |
title_short | Baricitinib: A Review in Moderate to Severe Atopic Dermatitis |
title_sort | baricitinib: a review in moderate to severe atopic dermatitis |
topic | Adis Drug Evaluation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9061224/ https://www.ncbi.nlm.nih.gov/pubmed/35503162 http://dx.doi.org/10.1007/s40257-022-00684-1 |
work_keys_str_mv | AT hoysheridanm baricitinibareviewinmoderatetosevereatopicdermatitis |