Study Condition(s): Migraine

A Study of Lasmiditan in Participants With Migraine

Study Alias: LAHC

Study Identifier(s): Tool Tip Icon {{ defaultRegistry.registryAnchorText }} NCT03247790 {{ currentLocaleObject.registryAnchorText }}

Recruiting Recruiting

Study Purpose

The purpose of this study is to measure how much of the drug gets into the blood stream and how long it takes the body to get rid of it during an acute migraine attack and also during the time between acute migraine attacks.

Key Participation Requirements Tool Tip Icon

All clinical trials have rules about who can participate. This section outlines some of those rules. Please contact a study center to discuss the full set of criteria

Gender

Male Female

Age

18+ years

Time Commitment

Your participation could last approximately 6 weeks and may include overnight stays
  • Participant must have a history of migraine with or without aura, for at least 1 year
  • Participant must not have participated in a clinical study involving an investigational product within the last 30 days
  • Participant must not have a history of or current irritable bowel syndrome
  • Participant must not have used or intend to use any migraine prevention treatments (including, but not limited to, propranolol or topiramate) within 30 days of the first dose of study drug and during the study

Where to Participate

3 locations are currently available of 72 planned
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