Effect of a rescue or recurrence dose of lasmiditan on efficacy and safety in the acute treatment of migraine: findings from the phase 3 trials (SAMURAI and SPARTAN)

被引:23
|
作者
Loo, Li Shen [1 ]
Plato, Brian M. [2 ]
Turner, Ira M. [3 ]
Case, Michael G. [1 ]
Raskin, Joel [1 ]
Dowsett, Sherie A. [1 ]
Krege, John H. [1 ]
机构
[1] Eli Lilly & Co, Corp Ctr, Indianapolis, IN 46285 USA
[2] Norton Neurosci Inst, 3991 Dutchmans Ln 4610, Louisville, KY 40207 USA
[3] Isl Neurol Associates PC, Ctr Headache Care & Res, Affiliate ProHealthcare, 824 Old Country Rd, Plainview, NY 11803 USA
关键词
Lasmiditan; Rescue; Recurrence; Second dose; Phase; 3; ORAL SUMATRIPTAN; TRIPTANS;
D O I
10.1186/s12883-019-1420-5
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background We studied the efficacy and safety of a second dose of lasmiditan for acute treatment of migraine. Methods SAMURAI and SPARTAN were double-blind, placebo-controlled Phase 3 studies in which individuals with migraine were randomized to oral lasmiditan 50 mg (SPARTAN only), 100 mg, 200 mg, or placebo. Study drug was to be taken within 4 h (h) of onset of a migraine attack (moderate or severe pain). A second dose of study drug was provided for rescue (patient not pain-free at 2 h and took a second dose 2-24 h post-first dose) or recurrence (patient pain-free at 2 h, but experienced recurrence of mild, moderate, or severe migraine pain and took a second dose 2-24 h after first dose). Randomization to second dose occurred at baseline; patients originally assigned lasmiditan were randomized to the same lasmiditan dose or placebo (2:1 ratio), and those originally assigned placebo received placebo. Data from SAMURAI and SPARTAN were pooled for efficacy and safety assessment of a second dose of lasmiditan. Results The proportion of patients taking a second dose was lower with lasmiditan versus placebo, and decreased with increasing lasmiditan dose; the majority who took a second dose did so for rescue. In patients taking lasmiditan as first dose, outcomes (pain free, most bothersome symptom [MBS] free) at 2 h after a second dose for rescue were similar whether the second dose was lasmiditan or placebo (p > 0.05 in all cases). In patients taking lasmiditan for first dose, outcomes at 2 h after a second dose for recurrence were as follows: lasmiditan pooled versus placebo - pain free, 50% vs 32% (p > 0.05); MBS free, 71% vs 41% (p = 0.02); pain relief, 77% vs 52% (p = 0.03). In patients whose first dose was lasmiditan, the incidence of treatment emergent adverse events (TEAEs) reported after the second dose was similar whether second dose was lasmiditan or placebo. Conclusions A second dose of lasmiditan showed some evidence of efficacy when taken for headache recurrence. There was no clear benefit of a second dose of lasmiditan for rescue treatment. The incidences of TEAEs were similar whether the second dose was lasmiditan or placebo.
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页数:8
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