drugset / Trial / NCT01484977
eValuation of the Efficacy and toleRability of Vimpat When Added to lEvetiracetam
NaSingle-groupOpen-labelTreatment
Summary
The main purpose of this study is to evaluate the effectiveness of the study drug lacosamide (200-600 mg/day) when added to a stable dose of levetiracetam (1000-3000 mg/day) with withdrawal of the concomitant sodium channel blocking-antiepileptic drug (AEDs) in subjects not well controlled on their current regimen.
Timeline
- Start
- 2011-12
- Primary completion
- 2013-12
- Completion
- 2013-12
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Lacosamide | Other / unclassified | 200 mg | — |
| Subject | Lacosamide | Other / unclassified | 600 mg | — |