NEUPRO (rotigotine) by UCB Pharma is dopamine agonists [moa]. Approved for nonergot dopamine agonist [epc]. First approved in 2007.
Drug data last refreshed 48m ago · AI intelligence enriched 1w ago
NEUPRO (rotigotine) is a nonergot dopamine agonist delivered via transdermal film for extended-release treatment of Parkinson's disease and restless legs syndrome. It works by stimulating dopamine receptors in the brain to restore motor control and reduce symptom burden. The transdermal delivery system provides continuous dopaminergic therapy with improved tolerability compared to oral formulations.
Peak-stage product with stable Medicare utilization (~79K claims annually) suggests mature brand team focused on retention and lifecycle management rather than aggressive expansion.
Dopamine Agonists
Nonergot Dopamine Agonist
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Bioequivalence and Adhesion of a Rotigotine Patch in Healthy Subjects
Clinical Trial to Investigate Patch Adhesion of Rotigotine Containing Patches in Patients With Parkinson's Disease
A Randomized, Open-Label, Crossover Study to Evaluate the Pharmacokinetic Profiles of Rotigotine After a Single Dose of LY03003 (28 mg) Versus After a Week of Daily NEUPRO® Transdermal Patch (4 mg Every 24 Hours) in Healthy Volunteers
A Follow-up Study of Rotigotine Patch in Adolescent Subjects With Restless Legs Syndrome
An Open, Randomised, Single Dose, 2-period, 2-sequence Crossover Adhesion Study of Two Different Transdermal Patches Containing Rotigotine.
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Upgrade to Pro — $25/moWorking on NEUPRO offers stable, mature-brand experience ideal for commercial professionals seeking deep expertise in chronic neurological disease management and transdermal delivery innovation. The near-term LOE horizon (5.5 years) requires strategic thinking on lifecycle extension and post-LOE transition, making this role suitable for mid-to-senior professionals planning portfolio diversification.