Aripiprazole Open-Label, Safety and Tolerability Study (APEX 241)

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Otsuka Pharmaceutical Development & Commercialization, Inc.
ClinicalTrials.gov Identifier:
NCT00102518
First received: January 29, 2005
Last updated: July 31, 2012
Last verified: July 2012
  Purpose

The purpose of this study is to test the long-term safety and tolerability of aripiprazole in adolescent patients with schizophrenia, and child and adolescent patients with bipolar I disorder, manic or mixed episode.


Condition Intervention Phase
Schizophrenia
Bipolar Disorder
Drug: Aripiprazole
Phase 3

Study Type: Interventional
Study Design: Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: A Multi-Center, Open-Label, Safety and Tolerability Study of Flexible-Dose Oral Aripiprazole (2 Mg-30 mg) in the Treatment of Adolescent Patients With Schizophrenia and Child and Adolescent Patients With Bipolar I Disorder, Manic or Mixed Episode With or Without Psychotic Features

Resource links provided by NLM:


Further study details as provided by Otsuka Pharmaceutical Development & Commercialization, Inc.:

Primary Outcome Measures:
  • Percentage of Subjects Experiencing SAEs [ Time Frame: Baseline and Week 23 ] [ Designated as safety issue: Yes ]
    Percentage of Subjects Experiencing SAEs. The incidences of SAEs are summarized by system organ class in CT-8.5.1; by system organ class and MedDRA preferred term and by system organ class, MedDRA preferred term, and severity.


Secondary Outcome Measures:
  • Change in Change in Positive and Negative Syndrome Scale (PANSS) Total Score [ Time Frame: Baseline and Week 26 ] [ Designated as safety issue: No ]

    Change from baseline to the last scheduled post-baseline evaluation in PANSS total score, using observed cases (assessments performed at baseline and weeks 4, 12, and 26).

    This scale consists of symptom constructs (7 positive, 7 negative, 16 general psychopathology), each to be rated on a 7-point scale of severity with 1 being absent to 7 being extreme. Minimum score is 30 which is best outcome; maximum score is 210 for worse outcome.


  • Change in Young Mania Rating Scale (Y-MRS) Total Score [ Time Frame: Baseline and Week 26 ] [ Designated as safety issue: No ]

    Change from baseline to last scheduled post-baseline evaluation in YMRS total score, using observed cases (assessments performed at baseline and weeks 4, 12, and 26).

    The Y-MRS consists of 11 items assessing the core symptoms of mania. Each item has 5 grades of severity. Minimum score on the scale is 0 (absent or normal). Maximum score on the scale is 60 (worse outcome or more severe symptoms).



Enrollment: 325
Study Start Date: September 2004
Study Completion Date: February 2007
Primary Completion Date: February 2007 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: NCT00102063 and NCT00110461 Subjects
All subjects had either completed or had withdrawn from the double-blind extension phase of study NCT00110461 (OPDC 31-03-240) and study NCT00102063 (OPDC 31-03-239).
Drug: Aripiprazole
2 to 30 mg/day orally (2, 5, 10, 15, 20, 25, or 30 mg/day); tablets in strengths of 2, 5, 10, and 15 mg were used to achieve desired doses
Other Name: OPC-14597

  Eligibility

Ages Eligible for Study:   10 Years to 17 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Adolescent patients with schizophrenia, or child and adolescent patients with bipolar I disorder, manic or mixed episode

Exclusion Criteria:

  • Patients with a co-morbid serious, uncontrolled systemic illness
  • Patients with a significant risk of committing suicide
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00102518

  Hide Study Locations
Locations
United States, Alabama
Local Institution
Birmingham, Alabama, United States
United States, Arkansas
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Little Rock, Arkansas, United States
United States, California
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Costa Mesa, California, United States
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Fresno, California, United States
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Orange, California, United States
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Riverside, California, United States
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Rosemead, California, United States
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Sacramento, California, United States
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Temecula, California, United States
United States, District of Columbia
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Washington, District of Columbia, United States
United States, Florida
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Altamonte Springs, Florida, United States
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Ft. Lauderdale, Florida, United States
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Hialeah, Florida, United States
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Jacksonville, Florida, United States
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Miami, Florida, United States
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Orange City, Florida, United States
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Tampa, Florida, United States
United States, Georgia
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Atlanta, Georgia, United States
United States, Hawaii
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Honolulu, Hawaii, United States
United States, Illinois
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Chicago, Illinois, United States
United States, Kansas
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Kansas City, Kansas, United States
United States, Kentucky
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Lexington, Kentucky, United States
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Louisville, Kentucky, United States
United States, Louisiana
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Lake Charles, Louisiana, United States
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Metairie, Louisiana, United States
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New Orleans, Louisiana, United States
United States, Massachusetts
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Somerville, Massachusetts, United States
United States, Michigan
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Clinton, Michigan, United States
United States, Missouri
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Kansas City, Missouri, United States
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St. Charles, Missouri, United States
United States, New York
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Elmsford, New York, United States
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New York, New York, United States
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Olean, New York, United States
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Rochester, New York, United States
United States, North Carolina
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Chapel Hill, North Carolina, United States
United States, Ohio
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Cleveland, Ohio, United States
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Lyndhurst, Ohio, United States
United States, Oklahoma
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Oklahoma City, Oklahoma, United States
United States, Pennsylvania
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Bala Cynwyd, Pennsylvania, United States
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Philadelphia, Pennsylvania, United States
United States, Tennessee
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Memphis, Tennessee, United States
United States, Texas
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Bellaire, Texas, United States
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DeSoto, Texas, United States
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Houston, Texas, United States
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San Antonio, Texas, United States
United States, Utah
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Salt Lake City, Utah, United States
United States, Washington
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Kirkland, Washington, United States
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Seattle, Washington, United States
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Spokane, Washington, United States
United States, Wisconsin
Local Institution
Wauwatosa, Wisconsin, United States
Sponsors and Collaborators
Otsuka Pharmaceutical Development & Commercialization, Inc.
  More Information

No publications provided

Responsible Party: Otsuka Pharmaceutical Development & Commercialization, Inc.
ClinicalTrials.gov Identifier: NCT00102518     History of Changes
Other Study ID Numbers: 31-03-241
Study First Received: January 29, 2005
Results First Received: May 16, 2012
Last Updated: July 31, 2012
Health Authority: United States: Food and Drug Administration

Keywords provided by Otsuka Pharmaceutical Development & Commercialization, Inc.:
Open Label
Aripiprazole
Bipolar I Disorder, Manic or Mixed Episode

Additional relevant MeSH terms:
Bipolar Disorder
Schizophrenia
Affective Disorders, Psychotic
Mood Disorders
Mental Disorders
Schizophrenia and Disorders with Psychotic Features
Aripiprazole
Antipsychotic Agents
Tranquilizing Agents
Central Nervous System Depressants
Physiological Effects of Drugs
Pharmacologic Actions
Central Nervous System Agents
Therapeutic Uses
Psychotropic Drugs

ClinicalTrials.gov processed this record on July 23, 2014