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A Study in Healthy Subjects to Determine the Effects When Alcohol is Administered With Perampanel

Central Nervous System Clinical Trial

Official title:
A Phase 1 Study in Healthy Subjects to Determine the Safety, Tolerability, Psychomotor Function and Cognitive Effects of Perampanel When Administered With Alcohol

Clinical Trial Summary

A Phase 1 study in healthy subjects to determine the safety, tolerability, psychomotor function, and cognitive effects of perampanel when administered alone and with alcohol.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Pharmacodynamics Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01531920
Study type Interventional
Source Eisai Inc.
Contact
Status Completed
Phase Phase 1
Start date May 2010
Completion date April 2011
View Details
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