Journal
CEPHALALGIA
Volume 42, Issue 2, Pages 108-118Publisher
SAGE PUBLICATIONS LTD
DOI: 10.1177/03331024211053571
Keywords
Erenumab; CGRP; migraine; topiramate; head-to-head study; prophylaxis
Categories
Funding
- Novartis
- Winicker Norimed GmbH
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In this study comparing erenumab to topiramate for migraine prophylaxis, erenumab demonstrated a more favorable tolerability and efficacy profile, with fewer patients discontinuing medication due to adverse events and significantly more patients achieving a >= 50% reduction in monthly migraine days.
Background: We compared the tolerability and efficacy of erenumab, a monoclonal antibody binding to the calcitonin gene-related peptide receptor, to topiramate for migraine prophylaxis in adults. Methods: HER-MES was a 24-week, randomised, double-blind, double-dummy, controlled trial conducted in 82 sites in Germany. Patients with >= 4 migraine days per month and naive to study drugs were randomly assigned (1:1) to either subcutaneous erenumab (70 or 140 mg/month) plus topiramate placebo (erenumab group) or oral topiramate at the individual dose with optimal efficacy (50-100 mg/day) plus erenumab placebo (topiramate group). The primary endpoint was medication discontinuation due to an adverse event during the double-blind phase. The proportion of patients that achieved >= 50% reduction from baseline in monthly migraine days during the last 3 months of the double-blind phase was a secondary endpoint. Results: Seven hundred and seventy-seven patients were randomised (from 22 February 2019 to 29 July, 2020) and 95.1% completed the study. In the erenumab group, 10.6% discontinued medication due to adverse events compared to 38.9% in the topiramate group (odds ratio, 0.19; 95% confidence interval 0.13-0.27; p < 0.001). Significantly more patients achieved a >= 50% reduction in monthly migraine days from baseline with erenumab (55.4% vs. 31.2%; odds ratio 2.76; 95% confidence interval 2.06-3.71; p < 0.001). No new safety signals occurred. Conclusions: Erenumab demonstrated a favourable tolerability and efficacy profile compared to topiramate.
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