drugset / Trial / NCT03376997

Study to Evaluate Bioavailability of a Single 12 mg Dose of Perampanel for Three Intravenous Infusion Durations Relative to a Single 12 mg Perampanel Oral Tablet in Healthy Subjects

NCT03376997

Phase 1 Completed 48 enrolled Eisai Inc.
RandomizedCrossoverOpen-labelBasic science

Summary

This study will be conducted to evaluate the bioavailability of a single 12 milligram (mg) dose of perampanel intravenous infusions of different durations relative to a single 12 mg dose of perampanel oral tablet in healthy participants.

Timeline

Start
2017-11-08
Primary completion
2018-02-16
Completion
2018-02-16

Drugs

EvaluationDrugModalityDoseRoute
Subject Perampanel Small molecule 12 mg Intravenous

Indications

No indication recorded.