Overview

Efficacy of YKP3089 in Patients With Photosensitive Epilepsy

Status:
Completed
Trial end date:
2010-01-01
Target enrollment:
Participant gender:
Summary
The aim of this study is to evaluate the ability of a single oral dose of YKP3089 to abolish or clearly reduce the IPS-induced photo-paroxysmal EEG response in photosensitive epilepsy patients, and to measure the onset and duration of the effect. Several cohorts will be used, to sequentially investigate different doses.
Phase:
Phase 2
Details
Lead Sponsor:
SK Life Science
SK Life Science, Inc.
Collaborator:
The Epilepsy Study Consortium
Treatments:
Cenobamate