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Almotriptan in the treatment of migraine
Almotriptan is an orally administered, highly selective serotonin 5-HT(1(B)/1(D)) receptor agonist that is effective in the acute treatment of moderate to severe migraine attacks. Since its introduction on to the market in 2001, several studies involving a large number of migraine patients have conf...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2656322/ https://www.ncbi.nlm.nih.gov/pubmed/19300615 |
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author | Sandrini, Giorgio Perrotta, Armando Arce Leal, Natalia L Buscone, Simona Nappi, Giuseppe |
author_facet | Sandrini, Giorgio Perrotta, Armando Arce Leal, Natalia L Buscone, Simona Nappi, Giuseppe |
author_sort | Sandrini, Giorgio |
collection | PubMed |
description | Almotriptan is an orally administered, highly selective serotonin 5-HT(1(B)/1(D)) receptor agonist that is effective in the acute treatment of moderate to severe migraine attacks. Since its introduction on to the market in 2001, several studies involving a large number of migraine patients have confirmed its efficacy and tolerability profile. Almotriptan, was found to be among the best-responding triptans in terms of pain relief and pain-free rate at 2 h. It has been reported that almotriptan has the best sustained pain-free (SPF) rate and the lowest adverse events (AEs) rate of all the triptans. When these clinical characteristics were combined to form the composite endpoint SPF and no AEs (SNAE), almotriptan emerged as the triptan with the best efficacy and tolerability profile. It also showed a good efficacy profile during the early treatment (within 1 h of onset) of migraine attacks characterized by moderate pain intensity. On the basis of these findings, almotriptan may be considered a therapeutic option for the acute treatment of migraine attacks. |
format | Text |
id | pubmed-2656322 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-26563222009-03-19 Almotriptan in the treatment of migraine Sandrini, Giorgio Perrotta, Armando Arce Leal, Natalia L Buscone, Simona Nappi, Giuseppe Neuropsychiatr Dis Treat Expert Opinion Almotriptan is an orally administered, highly selective serotonin 5-HT(1(B)/1(D)) receptor agonist that is effective in the acute treatment of moderate to severe migraine attacks. Since its introduction on to the market in 2001, several studies involving a large number of migraine patients have confirmed its efficacy and tolerability profile. Almotriptan, was found to be among the best-responding triptans in terms of pain relief and pain-free rate at 2 h. It has been reported that almotriptan has the best sustained pain-free (SPF) rate and the lowest adverse events (AEs) rate of all the triptans. When these clinical characteristics were combined to form the composite endpoint SPF and no AEs (SNAE), almotriptan emerged as the triptan with the best efficacy and tolerability profile. It also showed a good efficacy profile during the early treatment (within 1 h of onset) of migraine attacks characterized by moderate pain intensity. On the basis of these findings, almotriptan may be considered a therapeutic option for the acute treatment of migraine attacks. Dove Medical Press 2007-12 /pmc/articles/PMC2656322/ /pubmed/19300615 Text en © 2007 Dove Medical Press Limited. All rights reserved |
spellingShingle | Expert Opinion Sandrini, Giorgio Perrotta, Armando Arce Leal, Natalia L Buscone, Simona Nappi, Giuseppe Almotriptan in the treatment of migraine |
title | Almotriptan in the treatment of migraine |
title_full | Almotriptan in the treatment of migraine |
title_fullStr | Almotriptan in the treatment of migraine |
title_full_unstemmed | Almotriptan in the treatment of migraine |
title_short | Almotriptan in the treatment of migraine |
title_sort | almotriptan in the treatment of migraine |
topic | Expert Opinion |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2656322/ https://www.ncbi.nlm.nih.gov/pubmed/19300615 |
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