Lasmiditan is an effective acute treatment for migraine: A phase 3 randomized study

To assess the efficacy and safety of lasmiditan in the acute treatment of migraine. Adult patients with migraine were randomized (1:1:1) to a double-blind dose of oral lasmiditan 200 mg, lasmiditan 100 mg, or placebo and were asked to treat their next migraine attack within 4 hours of onset. Over 48...

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Published inNeurology Vol. 91; no. 24; p. e2222
Main Authors Kuca, Bernice, Silberstein, Stephen D, Wietecha, Linda, Berg, Paul H, Dozier, Gregory, Lipton, Richard B
Format Journal Article
LanguageEnglish
Published United States 11.12.2018
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Abstract To assess the efficacy and safety of lasmiditan in the acute treatment of migraine. Adult patients with migraine were randomized (1:1:1) to a double-blind dose of oral lasmiditan 200 mg, lasmiditan 100 mg, or placebo and were asked to treat their next migraine attack within 4 hours of onset. Over 48 hours after dosing, patients used an electronic diary to record headache pain and the presence of nausea, phonophobia, and photophobia, one of which was designated their most bothersome symptom (MBS). Of the 1,856 patients who treated an attack, 77.9% had ≥1 cardiovascular risk factors in addition to migraine. Compared with placebo, more patients dosed with lasmiditan 200 mg were free of headache pain at 2 hours after dosing (32.2% vs 15.3%; odds ratio [OR] 2.6, 95% confidence interval [CI] 2.0-3.6, < 0.001), similar to those dosed with lasmiditan 100 mg (28.2%; OR 2.2, 95% CI 1.6-3.0, < 0.001). Furthermore, compared with those dosed with placebo, more patients dosed with lasmiditan 200 mg (40.7% vs 29.5%; OR 1.6, 95% CI 1.3-2.1, < 0.001) and lasmiditan 100 mg (40.9%; OR 1.7, 95% CI, 1.3-2.2, < 0.001) were free of their MBS at 2 hours after dosing. Adverse events were mostly mild or moderate in intensity. Lasmiditan dosed at 200 and 100 mg was efficacious and well tolerated in the treatment of acute migraine among patients with a high level of cardiovascular risk factors. NCT02439320. This study provides Class I evidence that for adult patients with migraine, lasmiditan increases the proportion of subjects who are headache pain free at 2 hours after treating a migraine attack.
AbstractList To assess the efficacy and safety of lasmiditan in the acute treatment of migraine. Adult patients with migraine were randomized (1:1:1) to a double-blind dose of oral lasmiditan 200 mg, lasmiditan 100 mg, or placebo and were asked to treat their next migraine attack within 4 hours of onset. Over 48 hours after dosing, patients used an electronic diary to record headache pain and the presence of nausea, phonophobia, and photophobia, one of which was designated their most bothersome symptom (MBS). Of the 1,856 patients who treated an attack, 77.9% had ≥1 cardiovascular risk factors in addition to migraine. Compared with placebo, more patients dosed with lasmiditan 200 mg were free of headache pain at 2 hours after dosing (32.2% vs 15.3%; odds ratio [OR] 2.6, 95% confidence interval [CI] 2.0-3.6, < 0.001), similar to those dosed with lasmiditan 100 mg (28.2%; OR 2.2, 95% CI 1.6-3.0, < 0.001). Furthermore, compared with those dosed with placebo, more patients dosed with lasmiditan 200 mg (40.7% vs 29.5%; OR 1.6, 95% CI 1.3-2.1, < 0.001) and lasmiditan 100 mg (40.9%; OR 1.7, 95% CI, 1.3-2.2, < 0.001) were free of their MBS at 2 hours after dosing. Adverse events were mostly mild or moderate in intensity. Lasmiditan dosed at 200 and 100 mg was efficacious and well tolerated in the treatment of acute migraine among patients with a high level of cardiovascular risk factors. NCT02439320. This study provides Class I evidence that for adult patients with migraine, lasmiditan increases the proportion of subjects who are headache pain free at 2 hours after treating a migraine attack.
Author Lipton, Richard B
Dozier, Gregory
Berg, Paul H
Wietecha, Linda
Silberstein, Stephen D
Kuca, Bernice
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  organization: From CoLucid Pharmaceuticals (B.K.), Inc, Cambridge, MA; Thomas Jefferson University (S.D.S.), Philadelphia, PA; Eli Lilly and Company (L.W., P.H.B.), Indianapolis, IN; IQVIA (G.D.), Durham, NC; and Montefiore Headache Center (R.B.L.), Bronx, NY
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  email: wietecha_linda_a@lilly.com
  organization: From CoLucid Pharmaceuticals (B.K.), Inc, Cambridge, MA; Thomas Jefferson University (S.D.S.), Philadelphia, PA; Eli Lilly and Company (L.W., P.H.B.), Indianapolis, IN; IQVIA (G.D.), Durham, NC; and Montefiore Headache Center (R.B.L.), Bronx, NY. wietecha_linda_a@lilly.com
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  organization: From CoLucid Pharmaceuticals (B.K.), Inc, Cambridge, MA; Thomas Jefferson University (S.D.S.), Philadelphia, PA; Eli Lilly and Company (L.W., P.H.B.), Indianapolis, IN; IQVIA (G.D.), Durham, NC; and Montefiore Headache Center (R.B.L.), Bronx, NY
– sequence: 5
  givenname: Gregory
  surname: Dozier
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  organization: From CoLucid Pharmaceuticals (B.K.), Inc, Cambridge, MA; Thomas Jefferson University (S.D.S.), Philadelphia, PA; Eli Lilly and Company (L.W., P.H.B.), Indianapolis, IN; IQVIA (G.D.), Durham, NC; and Montefiore Headache Center (R.B.L.), Bronx, NY
– sequence: 6
  givenname: Richard B
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  organization: From CoLucid Pharmaceuticals (B.K.), Inc, Cambridge, MA; Thomas Jefferson University (S.D.S.), Philadelphia, PA; Eli Lilly and Company (L.W., P.H.B.), Indianapolis, IN; IQVIA (G.D.), Durham, NC; and Montefiore Headache Center (R.B.L.), Bronx, NY
BackLink https://www.ncbi.nlm.nih.gov/pubmed/30446595$$D View this record in MEDLINE/PubMed
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Snippet To assess the efficacy and safety of lasmiditan in the acute treatment of migraine. Adult patients with migraine were randomized (1:1:1) to a double-blind dose...
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SubjectTerms Acute Disease
Administration, Oral
Adult
Benzamides - therapeutic use
Dose-Response Relationship, Drug
Double-Blind Method
Female
Humans
Male
Middle Aged
Migraine Disorders - drug therapy
Piperidines - therapeutic use
Pyridines - therapeutic use
Treatment Outcome
Title Lasmiditan is an effective acute treatment for migraine: A phase 3 randomized study
URI https://www.ncbi.nlm.nih.gov/pubmed/30446595
Volume 91
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