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Elagolix: First Global Approval

Elagolix (ORILISSA™), an orally bioavailable, second-generation, non-peptide gonadotropin-releasing hormone (GnRH) receptor antagonist, is being developed AbbVie and Neurocrine Biosciences for the treatment of reproductive hormone-dependent disorders in women. In July 2018, the US FDA approved elago...

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Detalles Bibliográficos
Autor principal: Lamb, Yvette N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244606/
https://www.ncbi.nlm.nih.gov/pubmed/30194661
http://dx.doi.org/10.1007/s40265-018-0977-4
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author Lamb, Yvette N.
author_facet Lamb, Yvette N.
author_sort Lamb, Yvette N.
collection PubMed
description Elagolix (ORILISSA™), an orally bioavailable, second-generation, non-peptide gonadotropin-releasing hormone (GnRH) receptor antagonist, is being developed AbbVie and Neurocrine Biosciences for the treatment of reproductive hormone-dependent disorders in women. In July 2018, the US FDA approved elagolix tablets for the management of moderate to severe pain associated with endometriosis. This approval was based on positive results in two replicate phase III trials; additional phase III trials in the USA, Canada and Puerto Rico are currently evaluating elagolix as both monotherapy and in combination with low-dose hormone add-back therapy in the same indication. Elagolix with and without low-dose hormone add-back therapy is also undergoing phase III clinical development for heavy menstrual bleeding associated with uterine fibroids in the aforementioned locations. This article summarizes the milestones in the development of elagolix leading to its first approval for the management of moderate to severe pain associated with endometriosis.
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spelling pubmed-62446062018-12-04 Elagolix: First Global Approval Lamb, Yvette N. Drugs AdisInsight Report Elagolix (ORILISSA™), an orally bioavailable, second-generation, non-peptide gonadotropin-releasing hormone (GnRH) receptor antagonist, is being developed AbbVie and Neurocrine Biosciences for the treatment of reproductive hormone-dependent disorders in women. In July 2018, the US FDA approved elagolix tablets for the management of moderate to severe pain associated with endometriosis. This approval was based on positive results in two replicate phase III trials; additional phase III trials in the USA, Canada and Puerto Rico are currently evaluating elagolix as both monotherapy and in combination with low-dose hormone add-back therapy in the same indication. Elagolix with and without low-dose hormone add-back therapy is also undergoing phase III clinical development for heavy menstrual bleeding associated with uterine fibroids in the aforementioned locations. This article summarizes the milestones in the development of elagolix leading to its first approval for the management of moderate to severe pain associated with endometriosis. Springer International Publishing 2018-09-08 2018 /pmc/articles/PMC6244606/ /pubmed/30194661 http://dx.doi.org/10.1007/s40265-018-0977-4 Text en © Springer Nature 2018, corrected publication November/2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, duplication, 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 license and indicate if changes were made.
spellingShingle AdisInsight Report
Lamb, Yvette N.
Elagolix: First Global Approval
title Elagolix: First Global Approval
title_full Elagolix: First Global Approval
title_fullStr Elagolix: First Global Approval
title_full_unstemmed Elagolix: First Global Approval
title_short Elagolix: First Global Approval
title_sort elagolix: first global approval
topic AdisInsight Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244606/
https://www.ncbi.nlm.nih.gov/pubmed/30194661
http://dx.doi.org/10.1007/s40265-018-0977-4
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