Literature DB >> 31020659

Calcitonin Gene-Related Peptide Modulators - The History and Renaissance of a New Migraine Drug Class.

Richard Hargreaves1, Jes Olesen2.   

Abstract

Several lines of evidence pointed to an important role for CGRP in migraine. These included the anatomic colocalization of CGRP and its receptor in sensory fibers innervating pain-producing meningeal blood vessels, its release by trigeminal stimulation, the observation of elevated CGRP in the cranial circulation during migraine with normalization concomitant with headache relief by sumatriptan, and translational studies with intravenous (IV) CGRP that evoked migraine only in migraineurs. The development of small molecule CGRP receptor antagonists (CGRP-RAs) that showed clinical antimigraine efficacy acutely and prophylactically in randomized placebo-controlled clinical trials subsequently gave definitive pharmacological proof of the importance of CGRP in migraine. More recently, CGRP target engagement imaging studies using a CGRP receptor PET ligand [11 C]MK-4232 demonstrated that there was no brain CGRP receptor occupancy at clinically effective antimigraine doses of telcagepant, a prototypic CGRP-RA. Taken together, these data indicated that (1) the therapeutic site of action of the CGRP-RAs was peripheral not central; (2) that IV CGRP had most likely evoked migraine through an action at sites outside the blood-brain barrier; and (3) that migraine pain was therefore, at least in part, peripheral in origin. The evolution of CGRP migraine science gave impetus to the development of peripherally acting drugs that could modulate CGRP chronically to prevent frequent episodic and chronic migraine. Large molecule biologic antibody (mAb) approaches that are given subcutaneously to neutralize circulating CGRP peptide (fremanezumab, galcanezumab) or block CGRP receptors (erenumab) have shown consistent efficacy and tolerability in multicenter migraine prevention trials and are now approved for clinical use. Eptinezumab, a CGRP neutralizing antibody given IV, shows promise in late stage clinical development. Recently, orally administered next-generation small molecule CGRP-RAs have been shown to have safety and efficacy in acute treatment (ubrogepant and rimegepant) and prevention (atogepant) of migraine, giving additional CGRP-based therapeutic options for migraine patients.
© 2019 American Headache Society.

Entities:  

Keywords:  CGRP neutralizing antibody; CGRP receptor antagonist; CGRP receptor antibody; calcitonin gene-related peptide; migraine prevention; migraine treatment

Mesh:

Substances:

Year:  2019        PMID: 31020659     DOI: 10.1111/head.13510

Source DB:  PubMed          Journal:  Headache        ISSN: 0017-8748            Impact factor:   5.887


  22 in total

Review 1.  A Comprehensive Review of Zavegepant as Abortive Treatment for Migraine.

Authors:  Nazir Noor; Alexis Angelette; Abby Lawson; Anjana Patel; Ivan Urits; Omar Viswanath; Cyrus Yazdi; Alan D Kaye
Journal:  Health Psychol Res       Date:  2022-06-28

Review 2.  Drug Safety in Episodic Migraine Management in Adults Part 1: Acute Treatments.

Authors:  Yulia Y Orlova; Sandhya Mehla; Abigail L Chua
Journal:  Curr Pain Headache Rep       Date:  2022-05-10

Review 3.  Recent advances in targeting calcitonin gene-related peptide for the treatment of menstrual migraine: A narrative review.

Authors:  Yan Jiang; Zhen-Lun Huang
Journal:  Medicine (Baltimore)       Date:  2022-06-17       Impact factor: 1.817

4.  Fluorescently-labeled fremanezumab is distributed to sensory and autonomic ganglia and the dura but not to the brain of rats with uncompromised blood brain barrier.

Authors:  Rodrigo Noseda; Aaron J Schain; Agustin Melo-Carrillo; Jason Tien; Jennifer Stratton; Fanny Mai; Andrew M Strassman; Rami Burstein
Journal:  Cephalalgia       Date:  2019-12-19       Impact factor: 6.292

5.  Efficacy and safety of fremanezumab in patients with episodic and chronic migraine with documented inadequate response to 2 to 4 classes of migraine preventive medications over 6 months of treatment in the phase 3b FOCUS study.

Authors:  Messoud Ashina; Joshua M Cohen; Maja Galic; Verena Ramirez Campos; Steve Barash; Xiaoping Ning; Yoel Kessler; Lindsay Janka; Hans-Christoph Diener
Journal:  J Headache Pain       Date:  2021-07-10       Impact factor: 7.277

6.  Atogepant Is Not Associated With Clinically Meaningful Alanine Aminotransferase Elevations in Healthy Adults.

Authors:  K Chris Min; Walter K Kraft; Phung Bondiskey; Francheska Colón-González; Wen Liu; Jialin Xu; Deborah Panebianco; Lori Mixson; Marissa F Dockendorf; Catherine Z Matthews; Ramesh Boinpally
Journal:  Clin Transl Sci       Date:  2020-11-24       Impact factor: 4.689

7.  Single-Dose Pharmacokinetics and Safety of Atogepant in Adults With Hepatic Impairment: Results From an Open-Label, Phase 1 Trial.

Authors:  Ramesh Boinpally; Abhijeet Jakate; Matthew Butler; Lisa Borbridge; Antonia Periclou
Journal:  Clin Pharmacol Drug Dev       Date:  2021-01-27

8.  High rates of (treated) hypothyroidism among chronic migraine patients consulting a specialized headache clinic: are we missing something?

Authors:  Marcelo Filipchuk; Jesica Gassmann; Tatiana Castro Zamparella; Maria Cecilia Tibaldo; Mariela Carpinella; Pablo Sesto Tagliavini; Pablo Scarnato; Maria Teresa Goicochea; Osvaldo Bruera; Diego Martin Conci Magris; Marco Lisicki
Journal:  Neurol Sci       Date:  2021-07-20       Impact factor: 3.830

9.  Ubrogepant Is Not Associated With Clinically Meaningful Elevations of Alanine Aminotransferase in Healthy Adult Males.

Authors:  Wendy Ankrom; Phung Bondiskey; Chi-Chung Li; John Palcza; Wen Liu; Marissa F Dockendorf; Catherine Matthews; Deborah Panebianco; Tom Reynders; John A Wagner; Abhijeet Jakate; Sofie Mesens; Walter K Kraft; Eugene E Marcantonio
Journal:  Clin Transl Sci       Date:  2020-01-03       Impact factor: 4.689

Review 10.  The Emerging Role of Mechanosensitive Piezo Channels in Migraine Pain.

Authors:  Adriana Della Pietra; Nikita Mikhailov; Rashid Giniatullin
Journal:  Int J Mol Sci       Date:  2020-01-21       Impact factor: 5.923

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.