AbbVie submits tavapadon NDA in Parkinson’s
Chicago-based drugmaker AbbVie (NYSE: ABBV) has submitted a New Drug Application (NDA) to the US Food and Drug Administration (FDA) for tavapadon, a novel selective dopamine D1/D5 receptor partial agonist that was studied as a once daily oral treatment for Parkinson's disease.
The filing is based on results from the TEMPO clinical development program that evaluated the efficacy, safety and tolerability of tavapadon across a broad Parkinson's disease population.
Today's oral standard of care isn't effective enough to manage symptoms
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