A Study to Demonstrate Bioequivalence Between 6 x 2 mg Tablets of Perampanel and a Single 12 mg Tablet of Perampanel in Healthy Subjects

• Status: Completed
• Trial end date: 2010-09-01
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this study is to investigate the bioequivalence between 6 x 2 mg tablets and one 12 mg tablet of perampanel in healthy subjects.

• Phase: Phase 1
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Eisai Inc.

Criteria

Inclusion Criteria:

• Healthy male or female subjects aged between 18-55 years.

• BMI of 18-32 kg/m ^2.

• Willing and able to provide written informed consent.

Exclusion criteria:

• Subjects taking prescribed or over the counter (OTC) medications in 2 weeks prior to screening.

• Subjects on special diets or dietary aids known to modulate drug metabolizing enzymes.

• Subjects who have taken inhibitor of CYP450 within 2 weeks of first dose.

• Subjects who have received any experimental drug in the 12 weeks prior to study drug treatment.

• Subjects with a history of alcohol abuse or who drink more than the recommended number of alcohol units per week.

• Subjects who consume more than five caffeinated beverages per day.

• Subjects who smoke more than 5 cigarettes per day.

• Subjects with a history of drug abuse or who have a positive urine drug screening test.

• Women who do not agree to use two methods of contraception.