Study to Determine the Effectiveness of Risperidone in Bipolar Disorder in Children and Adolescents

Bipolar Disorder Clinical Trial

Official title:

Research on the Effectiveness of Risperidone in Bipolar Disorder in Adolescents and Children (REACH): A Double-Blind, Randomized, Placebo-Controlled Study of the Efficacy and Safety of Risperidone for the Treatment of Acute Mania in Bipolar I Disorder

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00076115
• Other study ID #: CR003631
• Status: Completed
• Phase: Phase 3
• First received: January 14, 2004
• Last updated: June 6, 2011
• Start date: December 2003
• Est. completion date: December 2005

Study information

• Verified date: April 2010
• Source: Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

A clinical study to determine the safety and effectiveness of risperidone compared with placebo in the treatment of bipolar disorder (manic or mixed type) in children and adolescents aged 10 to 17 years.

Description:

Subjects will be aged 10 to 17 years with a diagnosis of Bipolar I disorder and suffering from a current mixed or manic episode. On enrollment, subjects will be assigned to receive 1 of 3 treatments (oral placebo tablets, oral risperidone tablets 0.5 to 2.5 mg, or oral risperidone tablets 3 to 6 mg), which will be administered daily for 3 weeks. Study medication will be increased to the target dosage during the first 7 days, then further increased within the target dosage range reached until maximum tolerated dose is reached by day 10. The maximum tolerated dose will be given for the last 12 days of the study. Risperidone (0.5 to 2.5 mg or 3 to 6 mg doses) or placebo given orally as 0.25, 0.5, 1, 2, 3, or 4 mg tablets (or matching placebo) each day for 3 weeks.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 13
• Est. completion date: December 2005
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 10 Years to 17 Years

Eligibility

Inclusion Criteria:

• Current primary diagnosis of bipolar I disorder, mania or mixed type

• Aged between 10 and 17 years

• Young Mania Rating Scale score greater than or equal to 20 at screening and baseline

Exclusion Criteria:

• Known or suspected history of substance dependence

• Significant risk for suicidal or violent behavior

• Received electroconvulsive treatment within 4 weeks of baseline

• Received a depot antipsychotic within 2 treatment cycle before baseline

• Is unable to swallow medication taken in the form of tablets

• Has a positive result for a urine drug screen done at baseline

• Known or suspected seizure disorder

• Hypothyroidism or hyperthyroidism, unless stabilized on appropriate medication for at least 3 months before screening

• Known or suspected history of hypersensitivity or intolerance to risperidone

• History of a poor antimanic response to risperidone when used in adequate doses for an adequate period as the sole antimanic agent

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Bipolar Disorder

Intervention

Drug:
• Risperidone

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The change in the total YMRS score from baseline at the 3-week endpoint
Secondary	Effects on secondary efficacy variables (YMRS response and onset of maintained response, Clinical Global Impression Scale - Bipolar Disorder [CGI-BP]), safety, tolerability, and pharmacokinetics.

External Links

•   Study to Determine the Effectivness of Risperidone in Bipolar Disorder in Children and Adolescents