Clinical Trials Directory

Trials / Completed

CompletedNCT01531920

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

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

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
59 (actual)
Sponsor
Eisai Limited · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGalcohol + placeboPart A alcohol + placebo
DRUGalcohol + perampanelPart A: alcohol + perampanel
DRUGperampanel + alcoholPart B: perampanel + alcohol
DRUGplacebo + alcoholPart B: placebo + alcohol

Timeline

Start date
2010-05-01
Primary completion
2011-04-01
Completion
2011-04-01
First posted
2012-02-13
Last updated
2012-02-13

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT01531920. Inclusion in this directory is not an endorsement.

A Study in Healthy Subjects to Determine the Effects When Alcohol is Administered With Perampanel (NCT01531920) · Clinical Trials Directory