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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01227668
Other study ID # CN138-603
Secondary ID
Status Completed
Phase Phase 4
First received October 22, 2010
Last updated March 31, 2014
Start date March 2011
Est. completion date June 2012

Study information

Verified date March 2014
Source Bristol-Myers Squibb
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether pediatric participants with irritability associated with autistic disorder who have responded to aripiprazole treatment will experience a relapse significantly later when continuing therapy with aripiprazole than will participants who receive placebo


Description:

Phase 1: Single blind/ Phase 2: Double blind


Recruitment information / eligibility

Status Completed
Enrollment 215
Est. completion date June 2012
Est. primary completion date June 2012
Accepts healthy volunteers No
Gender Both
Age group 6 Years to 17 Years
Eligibility Key Inclusion Criteria:

- Male or female children or adolescents, 6 to 17 years of age, inclusive, at the time of the baseline visit

- Meets current diagnostic criteria of the Diagnostic and Statistical Manual-of Mental Disorders IV-Text Revised for autistic disorder and displays behaviors such as tantrums, aggression, self-injurious behavior, or a combination of these problems. Diagnosis of autistic disorder will be confirmed by the Autism Diagnostic Interview-Revised.

- Participant or designated guardian or caregiver is able to comprehend and satisfactorily comply with the protocol requirements, in the opinion of the investigator.

- Demonstrates behaviors such as tantrums, aggression, or self-injury or a combination of these problems

- An Aberrant Behavior Checklist Irritability subscale score =18 AND a Clinical Global Impressions Severity score =4 at the Screening and Baseline Visits.

- Mental age of at least 24 months

Key Exclusion Criteria:

- Treatment resistant to neuroleptic medication, based on lack of therapeutic response to 2 different neuroleptics after treatment for at least 3 weeks each.

- Previous treatment with aripiprazole for at least 3 weeks duration at an adequate daily dose, without demonstrating a clinically meaningful response.

- Lifetime diagnosis of bipolar disorder, psychosis, or schizophrenia, or a current diagnosis of major depressive disorder

- Diagnosis of Pervasive Developmental Disorder-Not Otherwise Specified, Asperger's Syndrome, Rett's Syndrome, childhood disintegrative disorder, or Fragile X Syndrome

- History of neuroleptic malignant syndrome

- At significant risk for suicide based on history or routine psychiatric status examination

- A seizure within the past year

- History of severe head trauma or stroke

- History or current evidence of any unstable medical conditions that would expose the patient to undue risk of a significant adverse event or interfere with assessments of safety or efficacy during the course of the trial

- Weight lower than 15 kg

- Known allergy or hypersensitivity to aripiprazole or other dihidrocarbostyrils

- History of a clinically significant low white blood cell count or a drug-induced leukopenia/neutropenia

- Any other medically significant abnormal laboratory test or vital sign result or electrocardiogram finding

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Aripiprazole
Tablets, Oral, 2-15 mg, once daily, 13-42 weeks
Placebo
Tablets, Oral, 0 mg, once daily, 16 weeks

Locations

Country Name City State
United States Neurobehavioral Medicine Group Bloomfield Hills Michigan
United States Unc Chapel Hill Chapel Hill North Carolina
United States Cleveland Clinic Cleveland Ohio
United States University Hospitals Case Medical Center Cleveland Ohio
United States Ericksen Research And Development Clinton Utah
United States Kootenai Behavioral Health Center Coeur D'Alene Idaho
United States The Ohio State University Nisonger Center Columbus Ohio
United States Clinical Innovations, Inc. Costa Mesa California
United States Insite Clinical Research Desoto Texas
United States Harmonex Neuroscience Research, Inc Dothan Alabama
United States Sarkis Clinical Trials Gainesville Florida
United States Clinical Research Center Of New Jersey Gibbsboro New Jersey
United States Behavioral Research Specialists, Llc Glendale California
United States Cyn3rgy Research Gresham Oregon
United States Palm Springs Research Institute Hialeah Florida
United States Holston Medical Group Kingsport Tennessee
United States Center For Psychiatry And Behavioral Medicine, Inc Las Vegas Nevada
United States Kosair Charities Pediatric Clinical Research Unit Louisville Kentucky
United States Florida Clinical Research Center, Llc Maitland Florida
United States Miami Children'S Hospital Miami Florida
United States Neurocare, Inc. Newton Massachusetts
United States Childrens Specialty Gr., Pllc Norfolk Virginia
United States Cutting Edge Research Group Oklahoma City Oklahoma
United States Ou Physician'S Child Study Center Oklahoma City Oklahoma
United States Abbey Neuropsychology Clinic Palo Alto California
United States Drexel University College Of Medicine Philadelphia Pennsylvania
United States Southwest Autism Research And Resource Center Phoenix Arizona
United States Western Psychiatric Institute And Clinic Pittsburgh Pennsylvania
United States Virginia Treatment Center For Children Richmond Virginia
United States Ucsf - Lppi San Francisco California
United States Lsu Health Sciences Center Shreveport Louisiana
United States Institute For Behavioral Medicine, Llc Smyrna Georgia
United States Stanford University School Of Medicine Stanford California
United States Stony Brook University School Of Medicine Stony Brook New York
United States University Of South Florida Tampa Florida
United States Children'S Specialized Hosp Toms River New Jersey
United States Tulsa Clinical Research, Llc Tulsa Oklahoma
United States Children'S National Medical Center Washington District of Columbia

Sponsors (1)

Lead Sponsor Collaborator
Bristol-Myers Squibb

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Number of Participants With Death as Outcome, Serious Adverse Events (SAEs), Adverse Events (AEs) Leading to Discontinuation, and Treatment-related AEs During Phase 2 AE=any new unfavorable symptom, sign, or disease or worsening of a preexisting condition that may not have a causal relationship with treatment. SAE=a medical event that at any dose results in death, persistent or significant disability/incapacity, or drug dependency/abuse; is life-threatening, an important medical event, or a congenital anomaly/birth defect; or requires or prolongs hospitalization. Treatment-related=having certain, probable, possible, or missing relationship to study drug. Weekly from Weeks 1 through 16 (end of treatment) of Phase 2 Yes
Primary Percentage of Patients Relapsing by Week 16 Time of relapse=date when patient meets relapse criteria. There are 4 definitions for relapse: 1. Patient meets the following criteria for 2 consecutive visits: (a) Aberrant Behavior Checklist Irritability score =25% than score at end of Phase 1 AND (b) Clinical Global Impression Improvement scale rating of 'Much Worse' or 'Very Much Worse' relative to rating at end of Phase 1. If relapse criteria met at 1 visit, 2nd visit should occur in about 1 week to reevaluate whether relapse criteria are still met. 2. Patient discontinues for "Lost to Follow-up" after a visit in which he or she met Definition 1 criteria (a&b). 3. Patient begins a prohibited drug (whether a study investigator or outside source prescribed) to treat worsening symptoms of irritability of autistic disorder after a visit where patient met Definition 1 criteria (a&b). 4. Patient discontinues due to hospitalization for worsening symptoms of irritability or due to lack of efficacy based on investigator's assessment. From end of Phase 1 (Date of randomization) to Week 16 of Phase 2 and end of treatment No
Secondary Adjusted Mean Change From Baseline to Week 16 on the Aberrant Behavior Checklist Irritability (ABC-I) Subscale Score (Last Observation Carried Forward [LOCF]) ABC is an informant-based checklist used to assess and classify problem behaviors of children and adolescents with mental retardation. The 58 items are rated on a 4-point scale (0=not at all a problem to 3=the problem is severe in degree), and resolve into 5 subscales: 1) irritability, agitation; 2) lethargy, social withdrawal; 3) stereotypic behavior; 4) hyperactivity, noncompliance; and 5) inappropriate speech. The ABC can be completed by parents, special educators, psychologists, direct caregivers, nurses, and others knowing the participant. Psychometric assessment of the ABC indicates that its subscales have high internal consistency, adequate reliability, and established validity. The ABC-I Subscale Score ranges from 0 to 45, with a negative change in score signifying improvement. LOCF data set includes data recorded at a given visit or, if no observation was recorded at that visit, data carried forward from the prior visit. chg=change; BL=baseline; APR=aripiprazole; vs=versus. From Baseline (end of Phase 1) to Week 16 of Phase 2 No
Secondary Change From Baseline in Mean Clinical Global Impression Improvement (CGI-I) Scale Score at Week 16 (Last Observation Carried Forward [LOCF]) CG-I rating scale permits global evaluation of patient's improvement over time. At baseline (BL), CGI Severity of Illness assessment is performed, in which the clinician rates severity of patient's condition on a 7-point scale ranging from 1=no symptoms to 7=very severe symptoms. Higher total score=worse symptoms. At subsequent visits, clinician assesses patient's improvement relative to symptoms at baseline on CGI-I 7-point scale ranging from 1=very much improved to 7=very much worse. Since the drug targets irritability symptoms, the CGI focuses on severity of irritability secondary to autistic disorder. Lower score=more improved symptoms. LOCF data set includes data recorded at a given visit or, if nothing recorded, data areccarried forward from the prior visit. For secondary endpoints (endpt), hierarchical testing was used to keep overall experiment-wise type I error rate to <=0.05. diff=difference; IS=irritability scale; PA=primary analysis; signif=significance/significantly. From Baseline (end of Phase 1) to Week 16 of Phase 2 No
Secondary Number of Participants With Death as Outcome, Serious Adverse Events (SAEs), and Adverse Events (AEs) Leading to Discontinuation During Phase 1 AE=any new unfavorable symptom, sign, or disease or worsening of a preexisting condition that may not have a causal relationship with treatment. SAE=a medical event that at any dose results in death, persistent or significant disability/incapacity, or drug dependency/abuse; is life-threatening, an important medical event, or a congenital anomaly/birth defect; or requires or prolongs hospitalization. Weekly from Week 1 to Week 26 and continuously to end of treatment Yes