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NCT02636842 · ClinicalTrials.gov registry record · Phase 1

A Study of Aripiprazole Lauroxil in Subjects With Schizophrenia or Schizoaffective Disorder

A Phase 1 study of Schizophrenia and Schizoaffective Disorder, sponsored by Alkermes.

Completed
Registry status
Phase 1
Development phase
47
Enrollment target
6
Study locations

NCT02636842 is a Phase 1 study of Schizophrenia and Schizoaffective Disorder that has completed, run by Alkermes. The registered enrollment target is 47 participants, below the 219-participant average among 315 other Schizophrenia trials with a reported enrollment target (79% lower). The trial reports 6 study locations across 4 states.

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The verdict

NCT02636842, a Phase 1 study of Schizophrenia and Schizoaffective Disorder, has completed, sponsored by Alkermes.

COMPLETED
Registry status
Phase 1
Development phase
47 participants
Enrollment target
6
Study locations

Study Summary

The study will determine the safety, tolerability, and pharmacokinetics of aripiprazole lauroxil in adults with schizophrenia or schizoaffective disorder.

Interventions

  • DRUG Aripiprazole Lauroxil

Study Locations (6)

California

  • Alkermes Investigational Site - Cerritos
  • Alkermes Investigational Site - Lemon Grove
  • Alkermes Investigational Site - Oakland

Illinois

  • Alkermes Investigational Site - Hoffman Estates

New Jersey

  • Alkermes Investigational Site - Marlton

Texas

  • Alkermes Investigative Site - Dallas

Trial Details

FieldValue
Enrollment Target 47 participants
Start Date 2015-12
Est. Completion 2016-06
Phase Phase 1

Sponsor

Alkermes

66 total trials

What the Registry Record Tells You About NCT02636842

The ClinicalTrials.gov registry entry for NCT02636842 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 47 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 219-participant average among 315 other Schizophrenia trials with a reported enrollment target (79% lower). The listed sponsor is Alkermes, which has 66 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Schizophrenia appearing as the primary indexed condition, and to 1 intervention - of which Aripiprazole Lauroxil is the first listed.

NCT02636842 reports 6 study locations spanning 4 distinct geographic areas - top geographies include California, Illinois, New Jersey.

Frequently Asked Questions

What is clinical trial NCT02636842 about?

NCT02636842 is a clinical study titled "A Study of Aripiprazole Lauroxil in Subjects With Schizophrenia or Schizoaffective Disorder". The study will determine the safety, tolerability, and pharmacokinetics of aripiprazole lauroxil in adults with schizophrenia or schizoaffective disorder.

What is the current status of trial NCT02636842?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 47 participants. The study started on 2015-12. Estimated completion is 2016-06.

What conditions does trial NCT02636842 study?

This clinical trial studies the following conditions: Schizophrenia, Schizoaffective Disorder.

What interventions are being tested in trial NCT02636842?

The interventions under investigation include: Aripiprazole Lauroxil (DRUG).

Who is sponsoring clinical trial NCT02636842?

This trial is sponsored by Alkermes, which has 66 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02636842 being conducted?

This trial has 6 study locations across California, Illinois, New Jersey, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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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.