Acorda's Inbrija receives FDA approval

24 December 2018

Acorda Therapeutics’ (Nasdaq: ACOR) Inbrija (levodopa inhalation powder) on Friday became the first Food and Drug Administration-approved inhaled levodopa for the intermittent treatment of OFF episodes in people with Parkinson’s disease.

The FDA approval was based on a clinical program that included approximately 900 people with Parkinson’s on a carbidopa/levodopa regimen experiencing OFF episodes.

Acorda plans to launch Inbrija in the first quarter of 2019.

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