The regulatory clearance allows the once daily therapy to be prescribed and sold in the US market for the treatment of the neurodegenerative condition.
Wednesday, October 21, 2026
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Business25 days ago
AbbVie has received US regulatory authorization for a new Parkinson's disease treatment targeting adult patients. The US Food and Drug Administration approved the drug, marketed as Juvmo and known as tavapadon, to be administered as a once daily pill.

The regulatory clearance allows the once daily therapy to be prescribed and sold in the US market for the treatment of the neurodegenerative condition.
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