Clinical Trials Directory

Trials / Completed

CompletedNCT01396590

Demonstrate Bioequivalence Between 6 ? 2-mg Tablets of Perampanel and a Single 12-mg Tablet of Perampanel in Healthy Subjects

A Randomized, Open-label, Crossover Study to Demonstrate Bioequivalence Between 6 ? 2-mg Tablets of Perampanel and a Single 12-mg Tablet of Perampanel in Healthy Subjects

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

Summary

The purpose of this study is to determine that six 2-mg tablets of perampanel are bioequivalent to one 12-mg tablet of perampanel.

Conditions

Interventions

TypeNameDescription
DRUGPerampanel6 x 2 mg perampanel once per day
DRUGPerampanel12 mg perampanel once per day

Timeline

Start date
2010-12-01
Primary completion
2011-03-01
Completion
2011-03-01
First posted
2011-07-19
Last updated
2012-05-04

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01396590. Inclusion in this directory is not an endorsement.

Demonstrate Bioequivalence Between 6 ? 2-mg Tablets of Perampanel and a Single 12-mg Tablet of Perampanel in Healthy Sub (NCT01396590) · Clinical Trials Directory