Drug data last refreshed 18h ago · AI intelligence enriched 2w ago
VIMPAT (lacosamide) is a small-molecule antiepileptic drug approved in 2008 that selectively enhances slow inactivation of voltage-gated sodium channels to stabilize neuronal membranes and inhibit repetitive firing. It is indicated for partial-onset seizures in epilepsy patients and is administered orally with high bioavailability (~100%) and a 13-hour half-life. The drug shows dose-proportional pharmacokinetics with low inter-subject variability, supporting consistent dosing from 100-800 mg daily.
As LOE approaches in April 2026, commercial teams face declining revenue and potential downsizing, making this a transition period for brand role stability.
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/moWorking on VIMPAT offers experience in mature-market management and competitive defense, but limited growth upside as the product approaches loss of exclusivity in 2026. Roles on this brand emphasize tactical execution, market-share retention, and stakeholder management in a declining-revenue environment rather than launch momentum or expansion.