CREXONT (carbidopa and levodopa) by Viatris (2) is dopa decarboxylase inhibitors [moa]. Approved for parkinson disease. First approved in 2024.
Drug data last refreshed 3d ago · AI intelligence enriched 2w ago
CREXONT is an extended-release oral capsule combining carbidopa and levodopa, approved August 2024 by Viatris for Parkinson's disease treatment. It works by inhibiting DOPA decarboxylase, allowing levodopa to reach the brain and replenish dopamine levels in patients with motor dysfunction. This formulation represents a new delivery platform for a classic combination therapy.
Early-stage commercial launch with growth potential; entry product for brand teams to establish market presence against established carbidopa/levodopa competitors.
DOPA Decarboxylase Inhibitors
Aromatic Amino Acid
Effect of BIA 9-1067 at Steady-state on the Pharmacokinetics of Levodopa/Carbidopa and Levodopa/Benserazide
CREXONT offers early-career entry and mid-career advancement opportunities in a growth-stage neurology product within Viatris' established Parkinson's franchise. Professionals joining now will build the brand foundation in a competitive specialty care landscape with long patent protection and multiple therapeutic areas to leverage.
Worked on CREXONT at Viatris (2)? Share your interview experience or compensation data (+7 days Pro)
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
Upgrade to Pro to access patent cliff timelines and LOE dates and other premium pharma intelligence.
Upgrade to Pro — $25/moUpgrade to Pro to access CMS Part B ASP pricing data and other premium pharma intelligence.
Upgrade to Pro — $25/mo