Patients were randomised to receive subcutaneous placebo, erenumab 70 mg, or erenumab 140 mg, given every 4 weeks for 12 weeks.
In a related editorial, the authors comment that future studies of erenumab should investigate longer-term efficacy and safety and the optimum dose for clinical practice, considering that the 70 mg and 140 mg doses proved similar in the short-term protocol. Treatment costs versus reduction of costs linked to migraine improvement also deserve consideration.
Erenumab is the first monoclonal antibody currently under phase III investigation for migraine prophylaxis.