Drug data last refreshed 2d ago · AI intelligence enriched 5d ago
VIMPAT (lacosamide) is a small-molecule antiepileptic drug approved in 2010 for adjunctive treatment of partial-onset seizures. It works through a novel mechanism involving sodium channel modulation and enhancement of slow inactivation. The oral solution formulation enables flexible dosing for patients with epilepsy.
Moderate competitive pressure (30%) indicates a consolidating epilepsy market with declining team expansion opportunities as LOE approaches in 2026.
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Lacosamide in Neonates With Repeated Electroencephalographic Neonatal Seizures
A Study to Test the Long-term Use of Oral Lacosamide in Pediatric Study Participants Who Completed NCT01964560 (EP0034) or NCT00938912 (SP848) and Received Lacosamide Treatment
Evaluation of the Efficacy and Safety of Lacosamide in Pediatric Patients With Epilepsy
A Study to Investigate the Bioequivalence of Lacosamide 200mg Administered as Intravenous Solution and Oral Tablet in Healthy Chinese Male Subjects
Study to Investigate Safety and Tolerability of Intravenous Lacosamide in Children.
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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.
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Upgrade to Pro — $25/moCareer opportunities on VIMPAT are shrinking as the product approaches loss of exclusivity in April 2026. This is a defensive assignment focused on margin protection and generic transition planning rather than growth opportunity.