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Early onset of efficacy with erenumab in patients with episodic and chronic migraine.
Schwedt, Todd; Reuter, Uwe; Tepper, Stewart; Ashina, Messoud; Kudrow, David; Broessner, Gregor; Boudreau, Guy P; McAllister, Peter; Vu, Thuy; Zhang, Feng; Cheng, Sunfa; Picard, Hernan; Wen, Shihua; Kahn, Joseph; Klatt, Jan; Mikol, Daniel.
Affiliation
  • Schwedt T; Department of Neurology, Mayo Clinic, 5777 E Mayo Blvd, Phoenix, AZ, 85054, USA. Schwedt.Todd@mayo.edu.
  • Reuter U; Department of Neurology, Charité Universitätsmedizin Berlin, Berlin, Germany.
  • Tepper S; Geisel School of Medicine at Dartmouth, Hanover, NH, USA.
  • Ashina M; Danish Headache Center and Department of Neurology, Rigshospitalet Glostrup, Faculty of Medical and Health Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Kudrow D; California Medical Clinic for Headache, Santa Monica, CA, USA.
  • Broessner G; Department of Neurology, Headache Outpatient Clinic, Medical University of Innsbruck, Innsbruck, Austria.
  • Boudreau GP; Clinique de la Migraine et Céphalées, Département de Neurologie, Centre Hospitalier de L'Université de Montréal, Hôpital Notre-Dame, Montréal, QC, Canada.
  • McAllister P; New England Institute for Neurology & Headache, Stamford, CT, USA.
  • Vu T; Amgen Inc., Thousand Oaks, CA, USA.
  • Zhang F; Amgen Inc., Thousand Oaks, CA, USA.
  • Cheng S; Amgen Inc., Thousand Oaks, CA, USA.
  • Picard H; Amgen Inc., Thousand Oaks, CA, USA.
  • Wen S; Novartis Pharmaceuticals Corp., East Hanover, NJ, USA.
  • Kahn J; Novartis Pharmaceuticals Corp., East Hanover, NJ, USA.
  • Klatt J; Novartis Pharma AG, Basel, Switzerland.
  • Mikol D; Amgen Inc., Thousand Oaks, CA, USA.
J Headache Pain ; 19(1): 92, 2018 Oct 01.
Article in En | MEDLINE | ID: mdl-30276500
ABSTRACT

BACKGROUND:

Subcutaneous erenumab reduced monthly migraine days and increased the likelihood of achieving a ≥ 50% reduction at all monthly assessment points tested in 2 pivotal trials in episodic migraine (EM) and chronic migraine (CM). Early efficacy of migraine preventive medications is an important treatment characteristic to patients. Delays in achievement of efficacy can result in failed adherence. The objective of these post-hoc analyses were to evaluate efficacy in the first 4 weeks after initial subcutaneous administration of erenumab 70 mg, erenumab 140 mg, or placebo.

METHODS:

There is no generally accepted methodology to measure onset of action for migraine preventive medications. We used a comprehensive approach with data from both studies to evaluate change from baseline in weekly migraine days (WMD), achievement of ≥ 50% reduction in WMD, and proportion of patients experiencing migraine measured on a daily basis. The 7-day moving averages were overlaid with observed data.

RESULTS:

In both studies (EM N = 955; CM N = 667), there was evidence of onset of efficacy of erenumab vs. placebo during the first week of treatment, which in some cases reached nominal significance. For EM the changes in WMD were (least squares mean [LSM] [95% CI]) placebo, - 0.1 (- 0.3, 0.0); erenumab 70 mg, - 0.3 (- 0.5, - 0.2) p = 0.130; erenumab 140 mg, - 0.6 (- 0.7, - 0.4) p < 0.001. For CM the changes were placebo, - 0.5 (- 0.8, - 0.3); erenumab 70 mg, - 0.9 (- 1.2, - 0.7) p = 0.047; erenumab 140 mg, - 0.8 (- 1.1, - 0.5) p = 0.18. Achievement of ≥ 50% reduction in WMD was observed as early as Week 1 (adjusted OR [95% CI] erenumab vs placebo) in EM erenumab 70 mg, 1.3 (1.0, 1.9) p = 0.097; erenumab 140 mg, 2.0 (1.4, 2.7) p < 0.001. A similar outcome was observed for CM erenumab 70 mg, 1.8 (1.1, 2.8) p = 0.011; erenumab 140 mg, 1.9 (1.2, 2.9) p = 0.009. Seven-day moving averages of observed data showed each treatment arm differed from placebo by Week 1 (OR [95% CI]) in EM Day 3 for erenumab 140 mg, 0.7 (0.5, 1.0) p = 0.031 and at Day 7 for 70 mg, 0.6 (0.4, 0.8) p = 0.002; in CM Day 6 for erenumab 70 mg, 0.6 (0.4, 0.9) p = 0.022 and at Day 7 for 140 mg, 0.7 (0.4, 1.0); p = 0.038.

CONCLUSION:

Erenumab showed early onset of efficacy with separation from placebo within the first week of treatment in both chronic and episodic migraine patients.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Internationality / Migraine Disorders / Antibodies, Monoclonal Type of study: Clinical_trials Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: J Headache Pain Journal subject: MEDICINA INTERNA / NEUROLOGIA / PSICOFISIOLOGIA Year: 2018 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Internationality / Migraine Disorders / Antibodies, Monoclonal Type of study: Clinical_trials Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: J Headache Pain Journal subject: MEDICINA INTERNA / NEUROLOGIA / PSICOFISIOLOGIA Year: 2018 Type: Article Affiliation country: United States