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Clinical Trial Summary

The primary purpose of the study is to assess pharmacodynamic (PD) activity of E2082 as measured by suppression of epileptic photoparoxysmal response (PPR) in the participant's most sensitive eye condition in participants with photosensitive epilepsy, compared to placebo.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03686033
Study type Interventional
Source Eisai Inc.
Contact
Status Terminated
Phase Phase 2
Start date October 31, 2018
Completion date June 18, 2019

See also
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Terminated NCT03603639 - A Study to Evaluate the Pharmacodynamic Activity of E2730 in Adult Participants With Photosensitive Epilepsy Phase 2
Completed NCT00609245 - Effect of Valproic Acid Concentration on Photic Response N/A