BACKGROUND: Efficacy and safety of erenumab have been evaluated in a comprehensive clinical development program resulting in approval for migraine prevention in over 40 countries to date. METHODS: This integrated safety analysis included four double-blind randomized trials and their extensions (up to three-plus years). Safety endpoints included exposure-adjusted patient incidences of adverse events, serious adverse events, and anti-erenumab antibodies. RESULTS: In all, 2375 of the patients randomized across the four studies received at least one dose of erenumab (70 mg or 140 mg), with cumulative exposure of 2641.2 patient-years. Exposure-adjusted adverse event rates during the double-blind treatment phase were similar to placebo, with the exception of injection-site reactions (17.1 vs. 10.8 per 100 patient-years), constipation (7.0 vs. 3.8 per 100 patient-years), and muscle spasm (2.3 vs. 1.2 per 100 patient-years). During the long-term extensions, adverse events reported were similar to those observed during the double-blind treatment phase, and rates of injection site reactions, constipation, and muscle spasm were reported at lower rates than in the double-blind treatment phase. There were two deaths reported, both confounded by pre-existing conditions. CONCLUSIONS: This pooled safety analysis revealed a favorable and stable adverse event profile over time for erenumab with more than three years of exposure. TRIAL REGISTRATION: ClinicalTrials.gov NCT01952574, NCT02483585, NCT02456740, NCT02066415, and NCT02174861.

Amgen Inc South San Francisco CA USA

Amgen Inc Thousand Oaks CA USA

California Medical Clinic for Headache Santa Monica CA USA

Dado Medical sro Prague Headache Center Prague Czech Republic

Danish Headache Center and Department of Neurology Rigshospitalet Glostrup Faculty of Health and Medical Sciences University of Copenhagen Glostrup Denmark

Department of Neurology Charité Universitätsmedizin Berlin Berlin Germany

Geisel School of Medicine at Dartmouth Hanover NH USA

Jefferson Headache Center Thomas Jefferson University Hospital Philadelphia PA USA

Novartis Pharma AG Basel Switzerland

Citace poskytuje Crossref.org

Zobrazit více v PubMed

ClinicalTrials.gov
NCT01952574, NCT02066415, NCT02483585, NCT02456740, NCT02174861