Abstract

BackgroundLasmiditan (LTN) is a selective 5-HT1F receptor agonist for the acute treatment of migraine in adults. We present detailed safety findings from the placebo-controlled, double-blind Phase 3 study, of LTN treatment across 4 attacks (CENTURION).MethodsPatients were randomized 1:1:1 to LTN 200 mg (LTN200), LTN100, or a control group that received placebo for 3 attacks and LTN50 for either the 3rd or 4th attack (1:1). Safety analyses were conducted for patients who took ≥1 dose of study drug and, in some cases, those who took all 4 doses.ResultsOverall, 1471 patients treated 4494 attacks. The incidences of treatment-emergent serious adverse events (SAEs) were - placebo, n=2 (0.4 %); LTN100, n=1 (0.2 %); LTN200, n=2 (0.4 %); no specific treatment-emergent SAE was reported in more than one patient. The most common treatment emergent adverse events (TEAEs) with lasmiditan were dizziness, paresthesia, fatigue, nausea, vertigo, and somnolence; the vast majority were mild or moderate in severity. The incidences of these TEAEs were highest during the first attack and decreased during subsequent attacks. For patients who experienced a common TEAE with the first attack, less than 45 % experienced the same event in subsequent attacks. Patients who did not experience an event in the 1st attack infrequently experienced the same event in subsequent attacks.The time of onset of the common TEAE ranged from ~40 min to 1 h (dependent upon TEAE) and, for individual TEAE, the onset was similar across attacks. Duration was dependent upon TEAE and attack. It was shortest for paresthesia (< 2 h for all attacks); it ranged from 1.8 to 5.5 h for other common TEAEs and was generally similar across attacks.Serotonin syndrome was reported for 2 patients post LTN dosing; there were no meaningful differences across treatment groups in suicidality; there was no evidence of an increase in motor vehicle accidents.ConclusionIn this blinded, controlled, multiple-attack study, LTN was associated with generally mild or moderate CNS-related TEAEs of short duration. TEAEs tended to decrease in frequency across the 4 attacks.Trial registrationNCT03670810

Highlights

  • The value of an acute treatment for migraine depends on its ability to rapidly and consistently relieve symptoms, and on acceptable drug safety and tolerability.Lasmiditan is a selective serotonin (5-HT1F) receptor agonist, approved in the US [1] and the United Arab Emirates for the acute treatment of migraine with or without aura in adults and being investigated in other geographies

  • Results of the 1613 patients randomized in CENTURION, 1471 (91 %) treated 1 or more migraine attacks with study drug and were considered the safety population; approximately half of those randomized (49 %) treated all 4 migraine attacks

  • For other common treatment emergent adverse events (TEAEs), time of onset ranged from ~40 min to 1 h; for each specific TEAE, the onset was similar across attacks (Table S2)

Read more

Summary

Introduction

Lasmiditan is a selective serotonin (5-HT1F) receptor agonist (ditan), approved in the US [1] and the United Arab Emirates for the acute treatment of migraine with or without aura in adults and being investigated in other geographies. In Phase 3 studies, lasmiditan was effective in the treatment of a migraine attack, as measured by pain freedom, pain relief, most bothersome symptom (MBS) freedom at 2 h, [2–4] and demonstrated a consistent response across attacks [4]. We report the detailed safety findings from the CENTURION study, a large Phase 3 placebo-controlled study designed to assess the efficacy, consistency, and safety of lasmiditan in acute treatment of 4 migraine attacks with or without aura. Lasmiditan (LTN) is a selective 5-HT1F receptor agonist for the acute treatment of migraine in adults. We present detailed safety findings from the placebo-controlled, double-blind Phase 3 study, of LTN treatment across 4 attacks (CENTURION)

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call