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Efficacy and safety of eptinezumab in patients with chronic migraine and medication-overuse headache: a randomized, double-blind, placebo-controlled study.
Yu, Shengyuan; Zhou, Jiying; Luo, Guogang; Xiao, Zheman; Ettrup, Anders; Jansson, Gary; Florea, Ioana; Ranc, Kristina; Pozo-Rosich, Patricia.
Afiliação
  • Yu S; Department of Neurology, Chinese PLA General Hospital, Beijing, China. yusy1963@126.com.
  • Zhou J; Department of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
  • Luo G; Neurology Department, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
  • Xiao Z; Department of Neurology, Renmin Hospital of Wuhan University, Wuhan, China.
  • Ettrup A; H. Lundbeck A/S, Copenhagen, Denmark.
  • Jansson G; H. Lundbeck A/S, Copenhagen, Denmark.
  • Florea I; H. Lundbeck A/S, Copenhagen, Denmark.
  • Ranc K; H. Lundbeck A/S, Copenhagen, Denmark.
  • Pozo-Rosich P; Neurology Department, Headache Unit, Vall d'Hebron University Hospital, Barcelona, Spain.
BMC Neurol ; 23(1): 441, 2023 Dec 15.
Article em En | MEDLINE | ID: mdl-38102535
ABSTRACT

BACKGROUND:

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 (11) 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).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos da Cefaleia Secundários / Transtornos de Enxaqueca Limite: Adolescent / Adult / Aged / Humans / Middle aged Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos da Cefaleia Secundários / Transtornos de Enxaqueca Limite: Adolescent / Adult / Aged / Humans / Middle aged Idioma: En Ano de publicação: 2023 Tipo de documento: Article