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Advances in CGRP Monoclonal Antibodies as Migraine Therapy: A Narrative Review

dc.Page.Noنوفمبر-18
dc.contributor.authorAditya, Suruchi
dc.contributor.authorRattan, Aditya
dc.date.accessioned2024-02-05T11:57:01Z
dc.date.available2024-02-05T11:57:01Z
dc.date.issued2023
dc.description.abstractMigraine is a potentially disabling disorder, yet it remains underdiagnosed and undertreated. The release of the neuropeptide calcitonin gene-related peptide (CGRP) in the trigemino-cerebrovascular system plays a vital role in the evolution of migraine. It enhances peripheral sensitization by mediating neurogenic inflammation and also influences central sensitization. The majority of the drug classes available for migraine prophylaxis are nonspecific and associated with numerous side effects and drug interactions. Anti-CGRP monoclonal antibodies (mAb) are an innovative therapeutic class that fulfills the need for more efficacious and tolerable preventive therapy. While erenumab is a mAb to the CGRP receptor, eptinezumab, fremanezumab, and galcanezumab bind to the CGRP molecule. They decrease the number of headache days and improve disability. Upper respiratory tract infection, nausea, constipation, pain at the site of injection, and fatigue are the associated side effects. CGRP mAbs are an excellent advancement in translational research and are a promising addition in migraine therapy. This article discusses the recent advances in the development of the CGRP mAbs.
dc.identifier.issn1658-631X
dc.identifier.urihttps://journals.lww.com/sjmm/fulltext/2023/11010/advances_in_cgrp_monoclonal_antibodies_as_migraine.2.aspx
dc.identifier.urihttps://repository.iau.edu.sa/handle/123456789/1087
dc.subjectAnti-CGRP antibody
dc.subjectCGRP
dc.subjectcalcitonin gene-related peptide receptors
dc.subjecteptinezumab
dc.subjecterenumab
dc.subjectfremanezumab
dc.subjectgalcanezumab
dc.subjectheadache
dc.subjectmigraine
dc.subjectmonoclonal antibodies
dc.titleAdvances in CGRP Monoclonal Antibodies as Migraine Therapy: A Narrative Review
dc.typeArticle

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