Drug data last refreshed 9h ago · AI intelligence enriched 1w ago
REYVOW (lasmiditan) is an oral small-molecule acute migraine treatment approved by the FDA in October 2019. It is a selective serotonin 5-HT1F receptor agonist designed to treat migraine with or without aura in adults. The mechanism targets migraine pathophysiology through a distinct serotonin receptor subtype.
Product is in peak commercial phase with modest Part D penetration (~11,500 claims in 2023), suggesting stable revenue but limited team expansion opportunities.
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 careers are concentrated in commercial and medical affairs functions typical of established small-molecule drugs in peak-cycle maturity. This product offers stable, long-term roles in brand management and field execution but limited upside in R&D or clinical expansion.