drugset / Trial / NCT01529515

A Study of Paliperidone Palmitate 3 Month Formulation for the Treatment of Patients With Schizophrenia

NCT01529515 ↗

Phase 3 Completed 509 enrolled Janssen Research & Development, LLC
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy of paliperidone palmitate 3 month formulation (PP3M) compared with placebo in delay of the time to first occurrence of relapse of the symptoms of schizophrenia.

Timeline

Start
2012-05
Primary completion
2014-04
Completion
2014-04

Outcome

Met primary endpoint

paper In the interim analysis, time to first relapse was significantly different in favor of the paliperidone palmitate group vs the placebo group PMID 25820612 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject paliperidone palmitate Unknown 175 mg Intramuscular
Subject paliperidone palmitate Unknown 263 mg Intramuscular
Subject paliperidone palmitate Unknown 350 mg Intramuscular
Subject paliperidone palmitate Unknown 525 mg Intramuscular

Indications