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Home » After delays, Abbvie wins FDA approval for Parkinson’s treatment
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After delays, Abbvie wins FDA approval for Parkinson’s treatment

Oct. 17, 2024
By Lee Landenberger
With two complete response letters in the rearview mirror, Abbvie Inc.’s Vyalev (foscarbidopa/foslevodopa) has been approved by the U.S. FDA for treating Parkinson’s disease. The drug is the first subcutaneous 24-hour infusion of levodopa-based therapy for treating motor fluctuations in adults with advanced disease.
BioWorld Clinical Regulatory Neurology/psychiatric Small molecule U.S. FDA

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