Treating Refractory Childhood Schizophrenia

Information

  • Research Project
  • 6528576
  • ApplicationId
    6528576
  • Core Project Number
    R01MH060229
  • Full Project Number
    5R01MH060229-02
  • Serial Number
    60229
  • FOA Number
  • Sub Project Id
  • Project Start Date
    9/1/2001 - 24 years ago
  • Project End Date
    7/31/2003 - 22 years ago
  • Program Officer Name
    VITIELLO, BENEDETTO
  • Budget Start Date
    8/1/2002 - 23 years ago
  • Budget End Date
    7/31/2003 - 22 years ago
  • Fiscal Year
    2002
  • Support Year
    2
  • Suffix
  • Award Notice Date
    8/10/2002 - 23 years ago

Treating Refractory Childhood Schizophrenia

DESCRIPTION (provided by applicant): Schizophrenia is a devastating illness regardless of the age at which it presents. When this disorder occurs in childhood or adolescence (onset of psychotic symptoms by age 17) the consequences in terms of functional impairment, loss of developmental opportunities, family suffering and societal burden are particularly dramatic. If young patients are refractory to treatment, the long-term outcome is likely to be considerably worse. In recent years, there has been considerable concern that very few data are available on the use of psychotropic drugs in young persons. This is no more apparent than in the antipsychotic treatment arena. Because of the evidence supporting the improved efficacy and/or side effect profile of the second-generation, or atypical antipsychotic medications in adults, and in the case of clozapine, in treatment refractory adults, it is essential to examine whether the potential benefits of these agents can be extended to children and particularly to treatment refractory children. This trial has been specifically targeted for children and adolescents with schizophrenia who have failed separate trials of olanzapine and risperidone at standard doses. Based on existing pilot and other data clozapine and olanzapine are the drugs of choice for this comparison. Specifically, we propose a 12-week, random-assignment, double-blind comparison of clozapine and high-dose olanzapine in 80 children and adolescents (ages 12 to 17) with treatment refractory schizophrenia (onset of psychotic symptoms by age 17). These treatment options represent viable and novel clinical treatments for patients and their families so that all trial participants, regardless of which treatment they are assigned to, will be receiving a new treatment option. Primary outcome measures will include: 1) overall drug response; 2) positive and negative symptoms; 3) adverse effects profiles. This trial will provide a basis to inform clinical treatment decisions and address the critical question as to whether clozapine or high-dose olazapine is more effective in seriously ill children and adolescents who do not respond to other agents.

IC Name
NATIONAL INSTITUTE OF MENTAL HEALTH
  • Activity
    R01
  • Administering IC
    MH
  • Application Type
    5
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    493659
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    242
  • Ed Inst. Type
  • Funding ICs
    NIMH:493659\
  • Funding Mechanism
  • Study Section
    ZMH1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    LONG ISLAND JEWISH MEDICAL CENTER
  • Organization Department
  • Organization DUNS
  • Organization City
    NEW HYDE PARK
  • Organization State
    NY
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    11040
  • Organization District
    UNITED STATES