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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00515320
Other study ID # NPL-2008-4-AUTUS-004
Secondary ID
Status Completed
Phase Phase 3
First received August 10, 2007
Last updated April 26, 2012
Start date August 2007
Est. completion date January 2009

Study information

Verified date April 2012
Source Neuropharm
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to assess the effect of fluoxetine orally dissolving tablets (ODT) on the repetitive behaviors core domain in children and adolescents with Autistic Disorder. The study will also investigate the effect of fluoxetine on the improvement of symptoms and the effects on daily living of the patient's family.


Recruitment information / eligibility

Status Completed
Enrollment 158
Est. completion date January 2009
Est. primary completion date January 2009
Accepts healthy volunteers No
Gender All
Age group 5 Years to 17 Years
Eligibility Inclusion Criteria:

- Meets DSM-IV criteria for autistic disorder, .

- CYBOCS-PDD score of at least 10 at screening.

Exclusion Criteria:

- Diagnosis of Asperger Syndrome or Pervasive Developmental Disorder Not Otherwise Specified, Rett Syndrome, Childhood Disintegrative Disorder.

- Patients planning to commence cognitive behaviour therapy during the period of the study or those who have begun cognitive behaviour therapy within 8 weeks prior to enrolment.

- Patients who are currently taking fluoxetine or who have previously taken it are not eligible for the study.

Other protocol-defined Inclusion/Exclusion criteria may apply.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Fluoxetine
Once daily oral dispersible tablet 2mg 9mg or 18mg
Placebo
Oral dispersible tablet placebo

Locations

Country Name City State
United States Long Island Jewish Hospital Bethpage New York
United States University of North Carolina Chapel Hill North Carolina
United States University of Illinois Chicago Illinois
United States Ohio State University Columbus Ohio
United States Children's Hospital of Michigan Detroit Michigan
United States University of Florida, Department of Psychiatry Gainesville Florida
United States Red Oak Psychiatry Associates Houston Texas
United States Center for Psychiatry and Behavioral Medicine Las Vegas Nevada
United States Harvard Medical School Medford Massachusetts
United States AMR-Baber Research Inc. Naperville Illinois
United States Mount Sinai School of Medicine New York New York
United States Southwest Autism Research and Resource Centre Phoenix Arizona
United States Western Psychiatric Institute and Clinic/ Merck Child Outpatient Clinic Pittsburgh Pennsylvania
United States University of California Davis Sacramento California
United States Seattle Children's Hosptial University of Washington Seattle Washington
United States Institute for Behavioral Medicine Smyrna Georgia
United States CRCNJ Voorhees New Jersey

Sponsors (2)

Lead Sponsor Collaborator
Neuropharm Autism Speaks

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary The percentage change from baseline to the endpoint visit for the CYBOCS-PDD score. Throughout the study
Secondary The time and dose related course of therapeutic effects Throughout the study
Secondary The inter-relationship between these effects in the context of global clinical changes. Throughout the study
Secondary The indirect effects on patient caregivers of the dose regime in these subjects compared to placebo during treatment. Throughout the study
Secondary Safety measures will be physical examination, vital signs, EKG/ECG & clinical laboratory tests. Throughout the study
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