drugset / Trial / NCT01515423

Study of Paliperidone Palmitate 3 Month and 1 Month Formulations for the Treatment of Patients With Schizophrenia

NCT01515423 ↗

Phase 3 Completed 1429 enrolled Janssen Research & Development, LLC
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to demonstrate that a paliperidone palmitate 3 month formulation (PP3M) is as effective as the paliperidone palmitate 1 month formulation (PP1M) in the treatment of patients with schizophrenia who have been stabilized on PP1M.

Timeline

Start
2012-05
Primary completion
2015-02
Completion
2015-03

Outcome

Met primary endpoint

paper Phase III results confirmed the hypothesis that efficacy of PP3M was noninferior to that of PP1M. PMID 27333588 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject paliperidone palmitate Unknown 50 mg Intramuscular
Subject paliperidone palmitate Unknown 75 mg Intramuscular
Subject paliperidone palmitate Unknown 100 mg Intramuscular
Subject paliperidone palmitate Unknown 150 mg Intramuscular
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