drugset / Trial / NCT03424564

Pharmacokinetic Study of Perampanel in Chinese Healthy Subjects

NCT03424564

Phase 1 Completed 44 enrolled Eisai Inc.
Non-randomizedParallel-groupOpen-labelBasic science

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.

Timeline

Start
2018-03-20
Primary completion
2018-05-25
Completion
2018-05-25

Drugs

EvaluationDrugModalityDoseRoute
Subject Perampanel Small molecule 2 mg Oral
Subject Perampanel Small molecule 4 mg Oral
Subject Perampanel Small molecule 8 mg Oral

Indications

No indication recorded.