Long-term safety and efficacy of erenumab in patients with chronic migraine: Results from a 52-week, open-label extension study
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články, multicentrická studie, randomizované kontrolované studie
PubMed
32216456
DOI
10.1177/0333102420912726
Knihovny.cz E-zdroje
- Klíčová slova
- Chronic migraine, efficacy, erenumab, long-term, open-label extension, preventive treatment, safety,
- MeSH
- antagonisté CGRP receptorů terapeutické užití MeSH
- dospělí MeSH
- humanizované monoklonální protilátky terapeutické užití MeSH
- lidé středního věku MeSH
- lidé MeSH
- migréna farmakoterapie MeSH
- senioři MeSH
- výsledek terapie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- randomizované kontrolované studie MeSH
- Názvy látek
- antagonisté CGRP receptorů MeSH
- erenumab MeSH Prohlížeč
- humanizované monoklonální protilátky MeSH
BACKGROUND: This study reports the long-term safety and efficacy of erenumab in chronic migraine patients. METHODS: This was a 52-week open-label extension study of a 12-week double-blind treatment phase study. During the double-blind treatment phase, patients received placebo or once-monthly erenumab 70 mg or 140 mg. During the open-label treatment phase, the initial monthly dose was erenumab 70 mg. Following protocol amendment, patients continued to receive erenumab 70 mg if they had already completed their Week 28 visit, otherwise, patients switched from 70 mg to 140 mg; if enrolled after the amendment, patients received 140 mg monthly throughout. RESULTS: In all, 451/609 (74.1%) enrolled patients completed the study. The exposure-adjusted patient incidence rate for any adverse event was 126.3/100 patient-years for the overall erenumab group. Overall, the adverse event profile was similar to that observed in the double-blind treatment phase. Adverse event incidence rates did not increase with long-term erenumab treatment compared with the double-blind treatment phase, and no new serious or treatment-emergent events were seen. Efficacy was sustained throughout the 52 weeks. Clinically significant reductions from double-blind treatment phase baseline (about half) were observed for monthly migraine days and migraine-specific medication days. Achievement of ≥50%, ≥75% and 100% reductions from the double-blind treatment phase baseline in monthly migraine days at Week 52 were reported by 59.0%, 33.2% and 8.9% of patients, respectively, for the combined dose group. A numerically greater benefit was observed with 140 mg compared with 70 mg at Weeks 40 and 52. CONCLUSIONS: Sustained efficacy of long-term erenumab treatment in patients with chronic migraine is demonstrated, with safety results consistent with the known safety profile of erenumab and adverse event rates comparable to placebo adverse event rates in the double-blind treatment phase. TRIAL REGISTRATION: This study is registered at ClinicalTrials.gov (NCT02174861).
Department of Neurology Charité Universitätsmedizin Berlin Berlin Germany
Geisel School of Medicine at Dartmouth Hanover NH USA
Global Biostatistical Science Amgen Inc Thousand Oaks CA USA
Global Development Amgen Inc Thousand Oaks CA USA
Jefferson Headache Center Thomas Jefferson University Philadelphia PA USA
Nashville Neuroscience Group and Vanderbilt University Department of Neurology Nashville TN USA
Prague Headache Center DADO MEDICAL sro Prague Czech Republic
Premiere Research Institute Nova Southeastern University West Palm Beach FL USA
Citace poskytuje Crossref.org
ClinicalTrials.gov
NCT02174861