Effectiveness and tolerability of eptinezumab in treating patients with migraine resistant to conventional preventive medications and CGRP (receptor) antibodies: a multicentre retrospective real-world analysis from Germany

Background Eptinezumab is a monoclonal antibody that targets calcitonin gene-related peptide (CGRP mAb) and is used for migraine prophylaxis. Efficacy data are mainly from clinical trials, real-world data are hardly available yet. Reimbursement policy in Germany leads to eptinezumab mainly being use...

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Veröffentlicht in:Journal of headache and pain 2024-05, Vol.25 (1), p.79-79, Article 79
Hauptverfasser: Scheffler, Armin, Wenzel, Pauline, Bendig, Merle, Gendolla, Astrid, Basten, Jale, Kleinschnitz, Christoph, Nsaka, Michael, Lindner, Diana, Naegel, Steffen, Burow, Philipp, Fleischmann, Robert, Holle, Dagny
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Sprache:eng
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Zusammenfassung:Background Eptinezumab is a monoclonal antibody that targets calcitonin gene-related peptide (CGRP mAb) and is used for migraine prophylaxis. Efficacy data are mainly from clinical trials, real-world data are hardly available yet. Reimbursement policy in Germany leads to eptinezumab mainly being used in patients having failed pre-treatment with other CGRP mAb. To date, it is unclear whether eptinezumab is efficacious and well tolerated in this population and how the treatment response differs from patients who are naive to CGRP mAbs. Methods We analysed clinical routine data of 79 patients (episodic migraine (EM): n  = 19; chronic migraine (CM): n  = 60) from four different centres in Germany. All patients were treated with eptinezumab (100mg). Differences in monthly headache (MHD), migraine (MMD) and acute medication days (AMD) after three months were analysed. The correlation of response with the number of CGRP mAb failures was evaluated. Significance level has been corrected (alpha = 0.017). Results After three months MHD, MMD and AMD were significantly reduced. In EM, the median reduction for MHD was 4.0 days (IQR: -6.5 to -1.0; p  = 0.001), for MMD 3.0 days (IQR: -5.5 to -1.5; p  
ISSN:1129-2377
1129-2369
1129-2377
DOI:10.1186/s10194-024-01788-1