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New dopamine agonist enters Parkinson disease care

  • By

  • Kathryn Wighton

  • September 29, 2026

  • 2 min

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  • 1

    The FDA approved tavapadon (Juvmo) for treating adults with Parkinson disease, as announced by AbbVie.

  • 2

    The approval was based on the phase 3 TEMPO clinical trial program evaluating tavapadon in early Parkinson disease.

  • 3

    In TEMPO-1, tavapadon improved daily living activities at week 26 compared to placebo, with significant score reductions.

  • 4

    TEMPO-3 showed that tavapadon increased daily 'on' time without troublesome dyskinesia compared to placebo.

  • 5

    Common mild to moderate adverse events included nausea, dizziness, and headache, with specific events varying by treatment.

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