4.8 Article

Fremanezumab for the Preventive Treatment of Chronic Migraine

Journal

NEW ENGLAND JOURNAL OF MEDICINE
Volume 377, Issue 22, Pages 2113-2122

Publisher

MASSACHUSETTS MEDICAL SOC
DOI: 10.1056/NEJMoa1709038

Keywords

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Funding

  1. Teva Pharmaceuticals
  2. Alder BioPharmaceuticals
  3. Allergan
  4. Amgen
  5. Automatic Technologies
  6. Avanir Pharmaceuticals
  7. Curelator
  8. Depomed
  9. Dr. Reddy's Laboratories
  10. electroCore
  11. Eli Lilly
  12. eNeura
  13. Insys Therapeutics
  14. Supernus Pharmaceuticals
  15. Theranica Bio-Electronics
  16. Trigemina
  17. Acorda Therapeutics
  18. Biocentric
  19. Biohaven
  20. Boston Scientific
  21. Charleston Laboratories
  22. CoLucid Pharmaceuticals
  23. Ladenburg Thalmann
  24. Magellan
  25. Merck
  26. Neuro Assessment Systems
  27. Pfizer
  28. Promius Pharma
  29. Tonix Pharmaceuticals
  30. Xenon Pharmaceuticals
  31. Zosano Pharma
  32. Akita Biomedical
  33. Alder Bio-Pharmaceuticals
  34. Cipla
  35. Novartis
  36. Quest Diagnostics
  37. Scion Pharmaceuticals

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BACKGROUND Fremanezumab, a humanized monoclonal antibody targeting calcitonin gene-related peptide (CGRP), is being investigated as a preventive treatment for migraine. We compared two fremanezumab dose regimens with placebo for the prevention of chronic migraine. METHODS In this phase 3 trial, we randomly assigned patients with chronic migraine (defined as headache of any duration or severity on >= 15 days per month and migraine on >= 8 days per month) in a 1:1:1 ratio to receive fremanezumab quarterly (a single dose of 675 mg at baseline and placebo at weeks 4 and 8), fremanezumab monthly (675 mg at baseline and 225 mg at weeks 4 and 8), or matching placebo. Both fremanezumab and placebo were administered by means of subcutaneous injection. The primary end point was the mean change from baseline in the average number of headache days (defined as days in which headache pain lasted >= 4 consecutive hours and had a peak severity of at least a moderate level or days in which acute migraine-specific medication [triptans or ergots] was used to treat a headache of any severity or duration) per month during the 12 weeks after the first dose. RESULTS Of 1130 patients enrolled, 376 were randomly assigned to fremanezumab quarterly, 379 to fremanezumab monthly, and 375 to placebo. The mean number of baseline headache days (as defined above) per month was 13.2, 12.8, and 13.3, respectively. The least-squares mean (+/- SE) reduction in the average number of headache days per month was 4.3 +/- 0.3 with fremanezumab quarterly, 4.6 +/- 0.3 with fremanezumab monthly, and 2.5 +/- 0.3 with placebo (P<0.001 for both comparisons with placebo). The percentage of patients with a reduction of at least 50% in the average number of headache days per month was 38% in the fremanezumab-quarterly group, 41% in the fremanezu-mab-monthly group, and 18% in the placebo group (P<0.001 for both comparisons with placebo). Abnormalities of hepatic function occurred in 5 patients in each fremanezumab group (1%) and 3 patients in the placebo group (<1%). CONCLUSIONS Fremanezumab as a preventive treatment for chronic migraine resulted in a lower frequency of headache than placebo in this 12-week trial. Injection-site reactions to the drug were common. The long-term durability and safety of fremanezumab require further study.

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