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Clinical Trial Summary

This will be a randomized, single dose, double-blind, placebo-controlled, Latin-square design with 5-period (full) crossover study with participants randomized to treatment sequences. Participants will complete all 5 Periods.

During each Period, participants will come to the clinical research unit (CRU) and remain overnight before being dosed with a single dose of either lasmiditan, alprazolam, or placebo in the morning. Cognitive testing and driving simulation will be conducted post dosing. Participants will have a washout of at least 5 days between each Period.

This study is designed to test non-inferiority of lasmiditan doses relative to placebo, with an alprazolam test versus placebo to confirm the sensitivity of the simulator to detect treatment effects.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03012334
Study type Interventional
Source Eli Lilly and Company
Contact
Status Completed
Phase Phase 1
Start date January 16, 2017
Completion date June 8, 2017

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