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New Generation Gepants: Migraine Acute and Preventive Medications
Migraine is a debilitating disease whose clinical and social impact is out of debate. Tolerability issues, interactions, contraindications, and inefficacy of the available medications make new options necessary. The calcitonin-gene-related peptide (CGRP) pathway has shown its importance in migraine...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8953732/ https://www.ncbi.nlm.nih.gov/pubmed/35329982 http://dx.doi.org/10.3390/jcm11061656 |
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author | Moreno-Ajona, David Villar-Martínez, María Dolores Goadsby, Peter J. |
author_facet | Moreno-Ajona, David Villar-Martínez, María Dolores Goadsby, Peter J. |
author_sort | Moreno-Ajona, David |
collection | PubMed |
description | Migraine is a debilitating disease whose clinical and social impact is out of debate. Tolerability issues, interactions, contraindications, and inefficacy of the available medications make new options necessary. The calcitonin-gene-related peptide (CGRP) pathway has shown its importance in migraine pathophysiology and specific medications targeting this have become available. The first-generation CGRP receptor antagonists or gepants, have undergone clinical trials but their development was stopped because of hepatotoxicity. The new generation of gepants, however, are efficacious, safe, and well tolerated as per recent clinical trials. This led to the FDA-approval of rimegepant, ubrogepant, and atogepant. The clinical trials of the available gepants and some of the newer CGRP-antagonists are reviewed in this article. |
format | Online Article Text |
id | pubmed-8953732 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-89537322022-03-26 New Generation Gepants: Migraine Acute and Preventive Medications Moreno-Ajona, David Villar-Martínez, María Dolores Goadsby, Peter J. J Clin Med Review Migraine is a debilitating disease whose clinical and social impact is out of debate. Tolerability issues, interactions, contraindications, and inefficacy of the available medications make new options necessary. The calcitonin-gene-related peptide (CGRP) pathway has shown its importance in migraine pathophysiology and specific medications targeting this have become available. The first-generation CGRP receptor antagonists or gepants, have undergone clinical trials but their development was stopped because of hepatotoxicity. The new generation of gepants, however, are efficacious, safe, and well tolerated as per recent clinical trials. This led to the FDA-approval of rimegepant, ubrogepant, and atogepant. The clinical trials of the available gepants and some of the newer CGRP-antagonists are reviewed in this article. MDPI 2022-03-16 /pmc/articles/PMC8953732/ /pubmed/35329982 http://dx.doi.org/10.3390/jcm11061656 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Moreno-Ajona, David Villar-Martínez, María Dolores Goadsby, Peter J. New Generation Gepants: Migraine Acute and Preventive Medications |
title | New Generation Gepants: Migraine Acute and Preventive Medications |
title_full | New Generation Gepants: Migraine Acute and Preventive Medications |
title_fullStr | New Generation Gepants: Migraine Acute and Preventive Medications |
title_full_unstemmed | New Generation Gepants: Migraine Acute and Preventive Medications |
title_short | New Generation Gepants: Migraine Acute and Preventive Medications |
title_sort | new generation gepants: migraine acute and preventive medications |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8953732/ https://www.ncbi.nlm.nih.gov/pubmed/35329982 http://dx.doi.org/10.3390/jcm11061656 |
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