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NCT00111189 · ClinicalTrials.gov registry record · Phase 3

A Study of the Efficacy (Effectiveness) of Paliperidone Palmitate in the Prevention of Recurrence of the Symptoms of Schizophrenia.

A Phase 3 study, sponsored by Johnson & Johnson Pharmaceutical Research & Development, L.L.C..

Completed
Registry status
Phase 3
Development phase
414
Enrollment target

NCT00111189 is a Phase 3 study that has completed, run by Johnson & Johnson Pharmaceutical Research & Development, L.L.C.. The registered enrollment target is 414 participants.

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The verdict

NCT00111189, a Phase 3 study, has completed, sponsored by Johnson & Johnson Pharmaceutical Research & Development, L.L.C..

COMPLETED
Registry status
Phase 3
Development phase
414 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the efficacy of paliperidone palmitate compared with placebo in the prevention of recurrence of the symptoms of schizophrenia and to assess the safety and tolerability of paliperidone palmitate in patients with stable and symptomatic schizophrenia. The placebo used in this study was a nutritional substance known as 20% Intralipid emulsion given to patients requiring intravenous feedings.

Interventions

  • DRUG Placebo
  • DRUG Paliperidone Palmitate

Trial Details

FieldValue
Enrollment Target 414 participants
Start Date 2005-02
Est. Completion 2008-02
Phase Phase 3

What the Registry Record Tells You About NCT00111189

The ClinicalTrials.gov registry entry for NCT00111189 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 414 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Johnson & Johnson Pharmaceutical Research & Development, L.L.C., which has 102 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT00111189 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00111189 about?

NCT00111189 is a clinical study titled "A Study of the Efficacy (Effectiveness) of Paliperidone Palmitate in the Prevention of Recurrence of the Symptoms of Schizophrenia.". The purpose of this study is to evaluate the efficacy of paliperidone palmitate compared with placebo in the prevention of recurrence of the symptoms of schizophrenia and to assess the safety and tolerability of paliperidone palmitate in patients with stable and symptomatic schizophrenia. The placeb...

What is the current status of trial NCT00111189?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 414 participants. The study started on 2005-02. Estimated completion is 2008-02.

What interventions are being tested in trial NCT00111189?

The interventions under investigation include: Placebo (DRUG), Paliperidone Palmitate (DRUG).

Who is sponsoring clinical trial NCT00111189?

This trial is sponsored by Johnson & Johnson Pharmaceutical Research & Development, L.L.C., which has 102 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.