A Study of the Effectiveness and Safety of Two Doses of Risperidone in the Treatment of Children and Adolescents With Autistic Disorder

Completed · Phase 4 · Has a placebo group

Conditions studied: Autistic Disorder, Autism

In brief

The purpose of this study is to evaluate the effectiveness (change in level of irritability and related behaviors) and safety and tolerability of the administration of 2 different fixed dose levels of risperidone (an atypical antipsychotic drug) compared with placebo in children or adolescents who have autism, and to evaluate the safety and tolerability of the drug for additional 26 weeks after the initial 6-week study period.

Key facts

Study ID

NCT00576732

Run by

Johnson & Johnson Pharmaceutical Research & Development, L.L.C.

People needed

96

Starts

2007-12-01

Expected to finish

2010-03-01

Last updated by the study team

2014-05-09

Who can join

Age: 5 and older, up to 17. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• DSM-IV diagnosis of Autistic Disorder (299.00)
• ABC-I Subscale score of greater than or equal to 18
• CGI-S of greater than or equal to 4
• mental age >18 months, body weight of at least 20 kg, seizure-free for at least 6 consecutive months and if on anticonvulsants must be on a dosage that has been stable for at least 4 weeks
• Medication free for 1 week before the start of the study for all psychotropic drugs, except 4 weeks for fluoxetine and at least 8 weeks for injectable medications
• Female patients must be premenarchal or sexually abstinent or, if heterosexually active, must practice an effective method of birth control.

You may not qualify if…

• History of prior or current DSM-IV psychotic disorder (e.g., schizophrenia, bipolar disorder, other psychosis), Pervasive Developmental Disorder not otherwise specified (PDD NOS), Asperger's, or Rett's
• Any history of hypersensitivity to risperidone, or its excipients in formulation, or other known drug allergy
• Patients who received risperidone within 3 months before screening (except p.r.n. use)
• Patients who did not demonstrate sufficient clinical response to an adequate trial of risperidone treatment in the past (an adequate trial is defined as a period of at least 4 weeks at an adequate dose)
• Neurologic disorder (e.g., Neuroleptic Malignant Syndrome, seizure disorders that are unstable, seizure activity within the past 6 months)
• History of alcohol or substance dependence within 3 months of screening
• Female subject who is pregnant (positive beta-HCG) or breast feeding
• Patients with existing moderate or severe EPS or history of tardive dyskinesia
• Patients who have received an experimental drug or used an experimental medical device within 3 months before the planned start of treatment.

Where it is running

• Study site — Dothan, Alabama, United States
• Study site — Phoenix, Arizona, United States
• Study site — Sacramento, California, United States
• Study site — Santa Ana, California, United States
• Study site — Boca Raton, Florida, United States
• Study site — Miami, Florida, United States
• Study site — Smyrna, Georgia, United States
• Study site — Hoffman Estates, Illinois, United States
• Study site — Naperville, Illinois, United States
• Study site — Lake Charles, Louisiana, United States
• Study site — Manhasset, New York, United States
• Study site — New York, New York, United States
• Study site — Staten Island, New York, United States
• Study site — The Bronx, New York, United States
• Study site — Columbus, Ohio, United States
• Study site — Oklahoma City, Oklahoma, United States
• Study site — Philadelphia, Pennsylvania, United States
• Study site — Houston, Texas, United States
• Study site — Fairfax, Virginia, United States
• Study site — Portsmouth, Virginia, United States

Full record on ClinicalTrials.gov

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