drugset / Trial / NCT02914314

Pharmacokinetic Study With an Oral Suspension of Perampanel as Adjunctive Therapy in Pediatric Subjects With Epilepsy

NCT02914314

Phase 2 Completed 26 enrolled Eisai Inc.
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the pharmacokinetics (PK) of perampanel during the Maintenance Period of the Core Study following oral suspension administration given as an adjunctive therapy in pediatric participants from 1 month to less than 4 years of age with epilepsy.

Timeline

Start
2017-02-20
Primary completion
2022-08-23
Completion
2023-04-25

Drugs

EvaluationDrugModalityDoseRoute
Subject Perampanel Small molecule 12 mg Oral
Subject Perampanel Small molecule 16 mg Oral

Indications