Eli Lilly & Co. has its second US approval in migraine in a little over one year, as the US Food and Drug Administration okayed Reyvow (lasmiditan) for the acute treatment of migraine on 11 October.
Lilly Expands Migraine Franchise With Reyvow Approval
Reyvow gives Lilly a second MOA in migraine, following the anti-CGRP biologic Emgality, and adds an acute therapy to the preventive agent approved in 2018.
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Pipeline Watch is a weekly snapshot of selected late-stage clinical trial events and approvals announced by pharmaceutical and biotech companies at medical and industry conferences, in financial and company presentations, and in company releases and statements.
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