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Daridorexant: First Approval
Daridorexant (Quviviq™; Idorsia Pharmaceuticals Ltd.) is an orally administered dual orexin type 1 and type 2 (OX(1) and OX(2)) receptor antagonist (DORA) being developed for the treatment of insomnia. It was selected from a pool of drug candidates on the basis of an expected effect duration of ≈ 8...
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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/PMC9042981/ https://www.ncbi.nlm.nih.gov/pubmed/35298826 http://dx.doi.org/10.1007/s40265-022-01699-y |
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author | Markham, Anthony |
author_facet | Markham, Anthony |
author_sort | Markham, Anthony |
collection | PubMed |
description | Daridorexant (Quviviq™; Idorsia Pharmaceuticals Ltd.) is an orally administered dual orexin type 1 and type 2 (OX(1) and OX(2)) receptor antagonist (DORA) being developed for the treatment of insomnia. It was selected from a pool of drug candidates on the basis of an expected effect duration of ≈ 8 h at a dose of 25 mg, with a half-life intended to minimize residual effects that might impair daytime functioning. Based on the results of two pivotal phase III trials, daridorexant was recently approved in the USA for the treatment of adult patients with insomnia characterized by difficulties with sleep onset and/or sleep maintenance. This article summarizes the milestones in the development of daridorexant leading to this first approval. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40265-022-01699-y. |
format | Online Article Text |
id | pubmed-9042981 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-90429812022-05-07 Daridorexant: First Approval Markham, Anthony Drugs AdisInsight Report Daridorexant (Quviviq™; Idorsia Pharmaceuticals Ltd.) is an orally administered dual orexin type 1 and type 2 (OX(1) and OX(2)) receptor antagonist (DORA) being developed for the treatment of insomnia. It was selected from a pool of drug candidates on the basis of an expected effect duration of ≈ 8 h at a dose of 25 mg, with a half-life intended to minimize residual effects that might impair daytime functioning. Based on the results of two pivotal phase III trials, daridorexant was recently approved in the USA for the treatment of adult patients with insomnia characterized by difficulties with sleep onset and/or sleep maintenance. This article summarizes the milestones in the development of daridorexant leading to this first approval. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40265-022-01699-y. Springer International Publishing 2022-03-17 2022 /pmc/articles/PMC9042981/ /pubmed/35298826 http://dx.doi.org/10.1007/s40265-022-01699-y 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 | AdisInsight Report Markham, Anthony Daridorexant: First Approval |
title | Daridorexant: First Approval |
title_full | Daridorexant: First Approval |
title_fullStr | Daridorexant: First Approval |
title_full_unstemmed | Daridorexant: First Approval |
title_short | Daridorexant: First Approval |
title_sort | daridorexant: first approval |
topic | AdisInsight Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042981/ https://www.ncbi.nlm.nih.gov/pubmed/35298826 http://dx.doi.org/10.1007/s40265-022-01699-y |
work_keys_str_mv | AT markhamanthony daridorexantfirstapproval |