Ubrogepant in the Acute Management of Migraine: A Narrative Review

Chia-Chun Chiang,1 Juliana H VanderPluym2 1Department of Neurology, Mayo Clinic, Rochester, MN, USA; 2Department of Neurology, Mayo Clinic, Scottsdale, AZ, USACorrespondence: Juliana H VanderPluym Email vanderpluym.juliana@mayo.eduAbstract: Ubrogepant is a small-molecule calcitonin gene-related pept...

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Main Authors: Chiang CC, VanderPluym JH
Format: Article
Language:English
Published: Dove Medical Press 2021-04-01
Series:Journal of Pain Research
Subjects:
Online Access:https://www.dovepress.com/ubrogepant-in-the-acute-management-of-migraine-a-narrative-review-peer-reviewed-fulltext-article-JPR
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spelling doaj-928078640f3a42c0b2cee0240bc1032d2021-04-27T20:04:10ZengDove Medical PressJournal of Pain Research1178-70902021-04-01Volume 141185119264246Ubrogepant in the Acute Management of Migraine: A Narrative ReviewChiang CCVanderPluym JHChia-Chun Chiang,1 Juliana H VanderPluym2 1Department of Neurology, Mayo Clinic, Rochester, MN, USA; 2Department of Neurology, Mayo Clinic, Scottsdale, AZ, USACorrespondence: Juliana H VanderPluym Email vanderpluym.juliana@mayo.eduAbstract: Ubrogepant is a small-molecule calcitonin gene-related peptide (CGRP) receptor antagonist that received Food and Drug Administration (FDA) approval for the acute treatment of migraine with and without aura in adults. The ACHIEVE I and ACHIEVE II Phase III clinical trials showed that ubrogepant was superior to placebo for pain freedom and freedom of the most bothersome migraine-associated symptom at 2 hours after medication intake. The 52-week open label extension of the Phase III trials demonstrated safety of ubrogepant. A real-world study conducted at a tertiary headache center also confirmed the efficacy and safety of ubrogepant. Adverse event rates were higher in the real-world population. Studies are needed to evaluate its long-term efficacy and safety, especially in the setting of co-administration with other CGRP modulating therapies such as the CGRP monoclonal antibodies.Keywords: ubrogepant, CGRP, migraine, Phase III trials, real-worldhttps://www.dovepress.com/ubrogepant-in-the-acute-management-of-migraine-a-narrative-review-peer-reviewed-fulltext-article-JPRubrogepantcgrpmigrainephase-3 trialsreal-world
collection DOAJ
language English
format Article
sources DOAJ
author Chiang CC
VanderPluym JH
spellingShingle Chiang CC
VanderPluym JH
Ubrogepant in the Acute Management of Migraine: A Narrative Review
Journal of Pain Research
ubrogepant
cgrp
migraine
phase-3 trials
real-world
author_facet Chiang CC
VanderPluym JH
author_sort Chiang CC
title Ubrogepant in the Acute Management of Migraine: A Narrative Review
title_short Ubrogepant in the Acute Management of Migraine: A Narrative Review
title_full Ubrogepant in the Acute Management of Migraine: A Narrative Review
title_fullStr Ubrogepant in the Acute Management of Migraine: A Narrative Review
title_full_unstemmed Ubrogepant in the Acute Management of Migraine: A Narrative Review
title_sort ubrogepant in the acute management of migraine: a narrative review
publisher Dove Medical Press
series Journal of Pain Research
issn 1178-7090
publishDate 2021-04-01
description Chia-Chun Chiang,1 Juliana H VanderPluym2 1Department of Neurology, Mayo Clinic, Rochester, MN, USA; 2Department of Neurology, Mayo Clinic, Scottsdale, AZ, USACorrespondence: Juliana H VanderPluym Email vanderpluym.juliana@mayo.eduAbstract: Ubrogepant is a small-molecule calcitonin gene-related peptide (CGRP) receptor antagonist that received Food and Drug Administration (FDA) approval for the acute treatment of migraine with and without aura in adults. The ACHIEVE I and ACHIEVE II Phase III clinical trials showed that ubrogepant was superior to placebo for pain freedom and freedom of the most bothersome migraine-associated symptom at 2 hours after medication intake. The 52-week open label extension of the Phase III trials demonstrated safety of ubrogepant. A real-world study conducted at a tertiary headache center also confirmed the efficacy and safety of ubrogepant. Adverse event rates were higher in the real-world population. Studies are needed to evaluate its long-term efficacy and safety, especially in the setting of co-administration with other CGRP modulating therapies such as the CGRP monoclonal antibodies.Keywords: ubrogepant, CGRP, migraine, Phase III trials, real-world
topic ubrogepant
cgrp
migraine
phase-3 trials
real-world
url https://www.dovepress.com/ubrogepant-in-the-acute-management-of-migraine-a-narrative-review-peer-reviewed-fulltext-article-JPR
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