A Long-term, Extended Treatment Study of Aripiprazole in Pediatric Patients With Schizophrenia

Exclusion Criteria

• •Patients who have a diagnosis of any other disease except schizophrenia, according to DSM-IV-TR
• •Patients who have been compulsorily admitted to hospital
• •Patients with mental retardation
• •Patients with thyroid disorder
• •Patients who fall under a contraindication listed in the ABILIFY package insert
• •Patients with a serious hepatic, renal, cardiac or hematopoietic disorder
• •Patients with a history or a complication of organic brain disorder or convulsive disorder such as epilepsy
• •Patients with a history or a complication of diabetes and patients who fall under any of the following: fasting blood glucose level ≧ 126 mg/dL, non-fasting blood glucose level ≧ 200 mg/dL, HbA1c ≧ 6.5%
• •Patients with a history or a complication of suicide attempt, suicidal thought or self-harm
• •Patients with a score of ≧2(mild) on PART1 evaluation of CGI-SS
• •Patients with a history or a complication of malignant syndrome, tardive dyskinesia or paralytic ileus
• •Patients in a state of physical exhaustion accompanied by such conditions as dehydration or malnutrition
• •Patients with a history or a complication of water intoxication
• •Patients with Parkinson's disease
• •Pregnant women, parturient women, nursing women, women of childbearing potential who wish to become pregnant during this trial. However, women of childbearing potential who are practicing an appropriate method of contraception (refer to 8.6) and have a negative pregnancy test result are eligible for inclusion in this study.
• •Study enrollment is otherwise judged to be inappropriate by the Investigator or Subinvestigator