drugset / Trial / NCT02682225

Crossover Study to Evaluate the Abuse Potential of Intranasal Esketamine Compared to Racemic Intravenous Ketamine in Nondependent, Recreational Drug Users

NCT02682225

Phase 1 Completed 55 enrolled Janssen Research & Development, LLC
RandomizedCrossoverDouble-blindTreatment

Summary

The primary objective of this study is to evaluate the abuse potential of intranasal esketamine (112 milligram and 84 mg) compared to racemic intravenous ketamine (0.5 mg/kg) in nondependent, recreational polydrug users of perception-altering drugs.

Timeline

Start
2016-03-25
Primary completion
2017-01-09
Completion
2017-01-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Esketamine Other / unclassified 84 mg Intranasal
Subject Esketamine Other / unclassified 112 mg Intranasal
Subject KETAMINE Small molecule 0.5 mg/kg Intravenous

Indications