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Tralokinumab: First Approval

Tralokinumab (Adtralza(®)) is a human IgG4 monoclonal antibody being developed by LEO Pharma for the treatment of atopic dermatitis. The T-helper cytokine IL-13 is thought to play a key role in the pathogenesis of atopic dermatitis. Tralokinumab specifically binds with high affinity to IL-13, inhibi...

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Detalles Bibliográficos
Autor principal: Duggan, Sean
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519819/
https://www.ncbi.nlm.nih.gov/pubmed/34406631
http://dx.doi.org/10.1007/s40265-021-01583-1
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author Duggan, Sean
author_facet Duggan, Sean
author_sort Duggan, Sean
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description Tralokinumab (Adtralza(®)) is a human IgG4 monoclonal antibody being developed by LEO Pharma for the treatment of atopic dermatitis. The T-helper cytokine IL-13 is thought to play a key role in the pathogenesis of atopic dermatitis. Tralokinumab specifically binds with high affinity to IL-13, inhibiting its interaction with the IL-13 receptor and thereby neutralising the biological activity of the cytokine. Based on results from the ECZTRA 1-3 trials, tralokinumab has recently been approved in the EU for the treatment of moderate-to-severe atopic dermatitis in adult patients who are candidates for systemic therapy. This article summarizes the milestones in the development of tralokinumab leading to this first approval for atopic dermatitis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40265-021-01583-1.
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spelling pubmed-85198192021-10-29 Tralokinumab: First Approval Duggan, Sean Drugs AdisInsight Report Tralokinumab (Adtralza(®)) is a human IgG4 monoclonal antibody being developed by LEO Pharma for the treatment of atopic dermatitis. The T-helper cytokine IL-13 is thought to play a key role in the pathogenesis of atopic dermatitis. Tralokinumab specifically binds with high affinity to IL-13, inhibiting its interaction with the IL-13 receptor and thereby neutralising the biological activity of the cytokine. Based on results from the ECZTRA 1-3 trials, tralokinumab has recently been approved in the EU for the treatment of moderate-to-severe atopic dermatitis in adult patients who are candidates for systemic therapy. This article summarizes the milestones in the development of tralokinumab leading to this first approval for atopic dermatitis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40265-021-01583-1. Springer International Publishing 2021-08-18 2021 /pmc/articles/PMC8519819/ /pubmed/34406631 http://dx.doi.org/10.1007/s40265-021-01583-1 Text en © Springer Nature 2021, corrected publication 2021 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 AdisInsight Report
Duggan, Sean
Tralokinumab: First Approval
title Tralokinumab: First Approval
title_full Tralokinumab: First Approval
title_fullStr Tralokinumab: First Approval
title_full_unstemmed Tralokinumab: First Approval
title_short Tralokinumab: First Approval
title_sort tralokinumab: first approval
topic AdisInsight Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519819/
https://www.ncbi.nlm.nih.gov/pubmed/34406631
http://dx.doi.org/10.1007/s40265-021-01583-1
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