drugset / Trial / NCT01559272

A Study to Assess the Pharmacokinetics, Safety, and Tolerability of Paliperidone Palmitate in Patients With Schizophrenia

NCT01559272

Phase 1 Completed 328 enrolled Janssen Research & Development, LLC
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the pharmacokinetics, safety, and tolerability of a paliperidone palmitate 3-month formulation in patients with schizophrenia.

Timeline

Start
2008-02-21
Primary completion
2014-04-09
Completion
2014-05-24

Drugs

EvaluationDrugModalityDoseRoute
Subject Paliperidone Unknown 1 mg Intramuscular
Subject Paliperidone Unknown 75 mg Intramuscular
Subject Paliperidone Unknown 150 mg Intramuscular
Subject Paliperidone Unknown 175 mg Intramuscular
Subject Paliperidone Unknown 300 mg Intramuscular
Subject Paliperidone Unknown 350 mg Intramuscular
Subject Paliperidone Unknown 450 mg Intramuscular
Subject Paliperidone Unknown 525 mg Intramuscular

Indications