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NCT00821600 · ClinicalTrials.gov registry record · Phase 1

Characterization of Intramuscular Injections of Risperidone 4 Week Long-acting Injectable (LAI) Formulation in the Buttock of Patients With Schizophrenia

A Phase 1 study, sponsored by Johnson & Johnson Pharmaceutical Research & Development, L.L.C..

Completed
Registry status
Phase 1
Development phase
24
Enrollment target

NCT00821600 is a Phase 1 study that has completed, run by Johnson & Johnson Pharmaceutical Research & Development, L.L.C.. The registered enrollment target is 24 participants.

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The verdict

NCT00821600, a Phase 1 study, has completed, sponsored by Johnson & Johnson Pharmaceutical Research & Development, L.L.C..

COMPLETED
Registry status
Phase 1
Development phase
24 participants
Enrollment target

Study Summary

The purpose of this study is to explore the pharmacokinetics, safety and tolerability of a 4-week long-acting injectable (LAI) formulation of risperidone after single intramuscular (i.m.) injection of 75 mg risperidone LAI in the gluteal muscle.

Interventions

  • DRUG risperidone IR and LAI formulation

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2008-12
Est. Completion 2009-06
Phase Phase 1

What the Registry Record Tells You About NCT00821600

The ClinicalTrials.gov registry entry for NCT00821600 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 24 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 1 intervention - of which risperidone IR and LAI formulation is the first listed.

NCT00821600 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00821600 about?

NCT00821600 is a clinical study titled "Characterization of Intramuscular Injections of Risperidone 4 Week Long-acting Injectable (LAI) Formulation in the Buttock of Patients With Schizophrenia". The purpose of this study is to explore the pharmacokinetics, safety and tolerability of a 4-week long-acting injectable (LAI) formulation of risperidone after single intramuscular (i.m.) injection of 75 mg risperidone LAI in the gluteal muscle.

What is the current status of trial NCT00821600?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 24 participants. The study started on 2008-12. Estimated completion is 2009-06.

What interventions are being tested in trial NCT00821600?

The interventions under investigation include: risperidone IR and LAI formulation (DRUG).

Who is sponsoring clinical trial NCT00821600?

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.