AbbVie Receives FDA's Approval For JUVMO To Treat Adults with Parkinson's Disease
AbbVie (NYSE: ABBV) today announced that the U.S. Food and Drug Administration (FDA) has approved JUVMO™ (tavapadon) tablets as the first and only selective D1/D5 receptor agonist for the treatment of adults with
AbbVie got permission to sell a new Parkinson's medicine called JUVMO. This shows the company is creating treatments people need, which could help its future business.
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