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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.author Yu, Shengyuan
dc.contributor.authorZhou, Jiying
dc.contributor.authorLuo, Guogang
dc.contributor.authorXiao, Zheman
dc.contributor.authorEttrup, Anders
dc.contributor.authorJansson, Gary
dc.contributor.authorPozo-Rosich, Patricia
dc.date.accessioned2024-01-08T10:45:31Z
dc.date.available2024-01-08T10:45:31Z
dc.date.issued2023-12-15
dc.identifier.citationYu S, Zhou J, Luo G, Xiao Z, Ettrup A, Jansson G, et al. Efficacy and safety of eptinezumab in patients with chronic migraine and medication-overuse headache: a randomized, double-blind, placebo-controlled study. BMC Neurol. 2023 Dec 15;23:441.
dc.identifier.issn1471-2377
dc.identifier.urihttps://hdl.handle.net/11351/10776
dc.descriptionChronic migraine; Eptinezumab; Preventive migraine treatment
dc.description.abstractBackground For some people with migraine, despite taking greater amounts of acute headache medication (AHM), they develop an increase in monthly headache days. This cycle of increasing headache days, and in turn AHM use, can lead to a secondary headache disorder called medication-overuse headache (MOH). Preventive medications can prevent migraine from occurring and reduce reliance on AHMs, thereby preventing the cycle of MOH. This study was performed to evaluate the efficacy and safety of eptinezumab to prevent migraine/headache in a mainly Asian patient population with a dual diagnosis of chronic migraine and MOH. Methods SUNLIGHT was a phase 3, multicenter, double-blind, parallel-group, placebo-controlled trial. Patients aged 18−75 years with ≥ 8 migraine days/month and a diagnosis of MOH were randomly allocated (1:1) to one of two treatment groups: eptinezumab 100 mg or placebo. Monthly migraine days (MMDs) were captured using a daily electronic diary; the change from baseline in the number of MMDs over Weeks 1−12 was the primary efficacy endpoint. Results Patients were randomized to eptinezumab 100 mg (n = 93) or placebo (n = 100). Over Weeks 1−12, eptinezumab reduced mean MMDs more than placebo (difference between treatments was -1.2; p = 0.1484). Differences between treatment groups with p-values below 0.05 favoring eptinezumab were observed in 3 out of the 6 key secondary endpoints. Conclusion All endpoints numerically favored eptinezumab treatment when compared to placebo; however, this study did not meet its primary endpoint and is therefore negative. No new safety signals were identified in this study, like previous reports that confirmed the safety and tolerability of eptinezumab treatment. Trial registration ClinicalTrials.gov identifier: NCT04772742 (26/02/2021).
dc.language.isoeng
dc.publisherBMC
dc.relation.ispartofseriesBMC Neurology;23
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScientia
dc.subjectAvaluació de resultats (Assistència sanitària)
dc.subjectAnticossos monoclonals - Ús terapèutic
dc.subjectMigranya - Tractament
dc.subject.meshAntibodies, Monoclonal
dc.subject.meshTreatment Outcome
dc.subject.meshMigraine Disorders
dc.titleEfficacy and safety of eptinezumab in patients with chronic migraine and medication-overuse headache: a randomized, double-blind, placebo-controlled study
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1186/s12883-023-03477-z
dc.subject.decsanticuerpos monoclonales
dc.subject.decsresultado del tratamiento
dc.subject.decstrastornos migrañosos
dc.relation.publishversionhttps://doi.org/10.1186/s12883-023-03477-z
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Yu S] Department of Neurology, Chinese PLA General Hospital, Beijing, China. [Zhou J] Department of Neurology, The First Afliated Hospital of Chongqing Medical University, Chongqing, China. [Luo G] Neurology Department, The First Afliated Hospital of Xi’an Jiaotong University, Xi’an, China. [Xiao Z] Department of Neurology, Renmin Hospital of Wuhan University, Wuhan, China. [Ettrup A, Jansson G] H. Lundbeck A/S, Copenhagen, Denmark. [Pozo Rosich P] Servei de Neurologia, Unitat de Cefalea, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Grup de Recerca de Cefalea i Dolor Neurològic, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Departament de Medicina, Universitat Autònoma de Barcelona, Bellaterra, Spain
dc.identifier.pmid38102535
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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