drugset / Trial / NCT02611505

A Study to Assess the Effects of Hepatic Impairment on the Pharmacokinetics, Safety, and Tolerability of Intranasally Administered Esketamine

NCT02611505

Phase 1 Completed 24 enrolled Janssen Research & Development, LLC
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the pharmacokinetics, safety, and tolerability of intranasally administered esketamine in both participants with varying stages of hepatic impairment and healthy participants.

Timeline

Start
2015-11-30
Primary completion
2017-02-27
Completion
2017-02-27

Drugs

EvaluationDrugModalityDoseRoute
Subject Esketamine Other / unclassified 28 mg Intranasal

Indications

No indication recorded.