Avadel Pharmaceuticals PLC said Monday that its Lumryz narcolepsy treatment received final approval from the U.S. Food and Drug Administration to address excessive day-time sleepiness.
Shares rose 14% to $12.04 at 13:31 E.T.
The pharmaceutical company said Lumryz is a single dose at bedtime that treats narcolepsy in adults, a chronic neurological condition that effects about one in 2,000 people in the U.S.
No comments:
Post a Comment
Note: Only a member of this blog may post a comment.