Rapid Onset and Sustained Efficacy of Lasmiditan Among Japanese Patients with Migraine: Prespecified Analyses of a Randomized Controlled Trial.

Abstract

Rapid onset and sustained efficacy are important for acute migraine treatment. Global phase3 trials have demonstrated the early onset and sustained efficacy of the 5-HT1F receptor agonist lasmiditan. In this prespecified analysis of the MONONOFU study, we assessed the onset and sustained efficacy of lasmiditan in Japanese patients with migraine. MONONOFU was a multicenter, randomized, placebo-controlled, phase2 study conducted in Japan (May 2019-June 2020). Eligible adults with migraine (N = 846; modified intent-to-treat population, N = 682) were randomized 7:3:7:6 to placebo, lasmiditan 50mg, 100mg, or 200mg, taken orally within 4h of moderate-to-severe migraine onset. Patients recorded headache severity and symptoms predose and 0.5-48h postdose. Sustained and modified sustained pain freedom were defined as patients who were headache pain-free 2h postdose and had no pain (sustained pain freedom) or had mild or no pain (modified sustained pain freedom) at 24 or 48h without rescue/recurrence medications. Efficacy outcomes were analyzed by logistic regression. Patients also recorded the actual time of pain-free and of meaningful pain relief (Kaplan-Meier analysis). Compared with placebo, significantly more lasmiditan-treated (100 or 200mg) patients were headache pain-free, had pain relief, were free of their most bothersome symptom, or had total migraine freedom (no headache or migraine-associated symptoms) within 30-60min. Median time to pain-free was 9.26, 6.88, 2.75, and 2.30h in placebo, 50-mg, 100-mg, and 200-mg lasmiditan groups, respectively. Significantly greater proportions of patients treated with 100 (19.7-29.5%) or 200mg (21.1-35.7%) lasmiditan had sustained or modified sustained pain freedom at 24 or 48h compared with placebo (10.4-15.8%). This prespecified analysis of data from MONONOFU has confirmed that the efficacy of lasmiditan is rapid in onset and sustained in patients with moderate-to-severe migraine in Japan. ClinicalTrials.gov (NCT03962738).