Eli Lilly’s (NYSE: LLY) 25 years spent researching headache disorders looks a little closer to paying off after a couple of announcements.
Firstly, the US pharma major has announced the submission of a New Drug Application (NDA) to the US Food and Drug Administration (FDA) for lasmiditan for the acute treatment of migraine with or without aura in adults.
Lasmiditan is an investigational, oral, centrally-penetrant, selective serotonin 5-HT1F agonist that is structurally and mechanistically distinct from other approved migraine therapies and lacks vasoconstrictive activity.
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