Drug data last refreshed 20h ago · AI intelligence enriched 3w ago
REYVOW (lasmiditan) is an oral small-molecule tablet approved by the FDA in October 2019 for the acute treatment of migraine. As a 5-HT1F receptor agonist, lasmiditan represents a novel mechanism distinct from traditional triptans, offering an alternative for patients who cannot tolerate or do not respond to existing migraine therapies. The product is currently in its peak lifecycle stage, marketed by Eli Lilly and Company.
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
A Study to Compare Two Different Formulations of Lasmiditan in Healthy Participants
A Study of Lasmiditan in Healthy Volunteers
A 12-Month Study of Lasmiditan (LY573144) Treatment in Children Aged 6 to 17 With Migraine
A Study of Lasmiditan (LY573144) Treatment in Children Aged 6 to 17 With Migraine
Lasmiditan Compared to Placebo in the Acute Treatment of Migraine in Korean
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
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Upgrade to Pro — $25/moREYVOW supports roles in brand management, medical science liaisons (MSLs), and field sales targeting neurology and primary care specialists who manage migraine patients. Success in this competitive space requires expertise in migraine pathophysiology, familiarity with CGRP mechanism differentiation, and ability to position against both established and newer competitors. Currently, zero open positions are linked to this product in the dataset, suggesting stable staffing or limited active hiring.