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CGRP as the target of new migraine therapies — successful translation from bench to clinic

Edvinsson, Lars LU ; Haanes, Kristian Agmund ; Warfvinge, Karin LU orcid and Krause, Diana N. LU (2018) In Nature Reviews Neurology 14(6). p.338-350
Abstract

Treatment of migraine is on the cusp of a new era with the development of drugs that target the trigeminal sensory neuropeptide calcitonin gene-related peptide (CGRP) or its receptor. Several of these drugs are expected to receive approval for use in migraine headache in 2018 and 2019. CGRP-related therapies offer considerable improvements over existing drugs as they are the first to be designed specifically to act on the trigeminal pain system, they are more specific and they seem to have few or no adverse effects. CGRP receptor antagonists such as ubrogepant are effective for acute relief of migraine headache, whereas monoclonal antibodies against CGRP (eptinezumab, fremanezumab and galcanezumab) or the CGRP receptor (erenumab)... (More)

Treatment of migraine is on the cusp of a new era with the development of drugs that target the trigeminal sensory neuropeptide calcitonin gene-related peptide (CGRP) or its receptor. Several of these drugs are expected to receive approval for use in migraine headache in 2018 and 2019. CGRP-related therapies offer considerable improvements over existing drugs as they are the first to be designed specifically to act on the trigeminal pain system, they are more specific and they seem to have few or no adverse effects. CGRP receptor antagonists such as ubrogepant are effective for acute relief of migraine headache, whereas monoclonal antibodies against CGRP (eptinezumab, fremanezumab and galcanezumab) or the CGRP receptor (erenumab) effectively prevent migraine attacks. As these drugs come into clinical use, we provide an overview of knowledge that has led to successful development of these drugs. We describe the biology of CGRP signalling, summarize key clinical evidence for the role of CGRP in migraine headache, including the efficacy of CGRP-targeted treatment, and synthesize what is known about the role of CGRP in the trigeminovascular system. Finally, we consider how the latest findings provide new insight into the central role of the trigeminal ganglion in the pathophysiology of migraine.

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author
; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Nature Reviews Neurology
volume
14
issue
6
pages
338 - 350
publisher
Nature Publishing Group
external identifiers
  • scopus:85045911106
  • pmid:29691490
ISSN
1759-4758
DOI
10.1038/s41582-018-0003-1
language
English
LU publication?
yes
id
3304fbcc-2508-4d78-83b6-d8c9753313e1
date added to LUP
2018-05-04 08:38:53
date last changed
2024-06-25 16:20:07
@article{3304fbcc-2508-4d78-83b6-d8c9753313e1,
  abstract     = {{<p>Treatment of migraine is on the cusp of a new era with the development of drugs that target the trigeminal sensory neuropeptide calcitonin gene-related peptide (CGRP) or its receptor. Several of these drugs are expected to receive approval for use in migraine headache in 2018 and 2019. CGRP-related therapies offer considerable improvements over existing drugs as they are the first to be designed specifically to act on the trigeminal pain system, they are more specific and they seem to have few or no adverse effects. CGRP receptor antagonists such as ubrogepant are effective for acute relief of migraine headache, whereas monoclonal antibodies against CGRP (eptinezumab, fremanezumab and galcanezumab) or the CGRP receptor (erenumab) effectively prevent migraine attacks. As these drugs come into clinical use, we provide an overview of knowledge that has led to successful development of these drugs. We describe the biology of CGRP signalling, summarize key clinical evidence for the role of CGRP in migraine headache, including the efficacy of CGRP-targeted treatment, and synthesize what is known about the role of CGRP in the trigeminovascular system. Finally, we consider how the latest findings provide new insight into the central role of the trigeminal ganglion in the pathophysiology of migraine.</p>}},
  author       = {{Edvinsson, Lars and Haanes, Kristian Agmund and Warfvinge, Karin and Krause, Diana N.}},
  issn         = {{1759-4758}},
  language     = {{eng}},
  number       = {{6}},
  pages        = {{338--350}},
  publisher    = {{Nature Publishing Group}},
  series       = {{Nature Reviews Neurology}},
  title        = {{CGRP as the target of new migraine therapies — successful translation from bench to clinic}},
  url          = {{http://dx.doi.org/10.1038/s41582-018-0003-1}},
  doi          = {{10.1038/s41582-018-0003-1}},
  volume       = {{14}},
  year         = {{2018}},
}