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CompletedNCT03424564

Pharmacokinetic Study of Perampanel in Chinese Healthy Subjects

A Single and Multiple Dose Pharmacokinetic Study of Perampanel in Chinese Healthy Subjects

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
44 (actual)
Sponsor
Eisai Co., Ltd. · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

This study will be conducted to evaluate the pharmacokinetics of perampanel following single and multiple oral doses in Chinese healthy male and female participants.

Conditions

Interventions

TypeNameDescription
DRUGPerampanelOral Tablet

Timeline

Start date
2018-03-20
Primary completion
2018-05-25
Completion
2018-05-25
First posted
2018-02-07
Last updated
2018-08-28

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03424564. Inclusion in this directory is not an endorsement.

Pharmacokinetic Study of Perampanel in Chinese Healthy Subjects (NCT03424564) · Clinical Trials Directory