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A Prospective Open-label Study of Aripiprazole in Fragile X Syndrome

Aripiprazole in Fragile X Syndrome

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00420459
Enrollment
12
Registered
2007-01-11
Start date
2007-04-30
Completion date
2010-03-31
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fragile X Syndrome

Brief summary

The purpose of this study is to determine the effectiveness and tolerability of aripiprazole in the treatment of children and adolescents with Fragile X Syndrome.

Detailed description

This 12-week prospective, open-label study design was chosen to gather pilot data for potential future lager scale, double-blind, placebo-controlled studies in Fragile X Syndrome. We hypothesize that aripiprazole will be effective in decreasing aggression, SIB, agitation, and interfering repetitive behavior commonly observed in individuals with Fragile X Syndrome. We also hypothesize that aripiprazole will be well tolerated.

Interventions

DRUGAripiprazole

All subjects will initially receive 2.5 mg/day of aripiprazole during the first week. The dosage may be increased to a maximum of 20 mg/day over 8 weeks.

Sponsors

Indiana University School of Medicine
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
5 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

1. Males and females between the ages of 5 and 35 years and 2. Body weight greater than or equal to 15 kg 3. Confirmed diagnosis of Fragile X Syndrome based upon genetic testing results. 4. Outpatients. 5. Psychotropic medication-free for at least 2 weeks prior to screening laboratory tests and electrocardiogram. (Except 5 weeks for fluoxetine and 4 weeks for all typical and atypical antipsychotics that have been administered for at least a 4 week period.) Exceptions to medication-free status will include drugs given at bedtime targeting insomnia. Such drugs may include melatonin, clonidine, chloral hydrate, diphenhydramine, ramelteon, benzodiazepines, or other sedative-hypnotics. 6. Clinical Global Impression Scale Severity score (CGI-S) of at greater than or equal to 4 (Moderately Ill) 7. A score of at greater than or equal to 18 on the Irritability subscale of the Aberrant Behavior Checklist (ABC) at screen and baseline. 8. Mental age of greater than or equal to 18 months as measured by the Wechsler, revised Leiter, or Mullen tests 9. Each subject must be in good physical health as determined by screening procedures which will include a detailed medical history, complete physical and neurological examination.

Exclusion criteria

1. DSM-IV diagnosis of schizophrenia, another psychotic disorder, bipolar disorder or alcohol or other substance abuse within the last 6 months. 2. A significant medical condition such as heart, liver, renal or pulmonary disease, or an actively treated seizure disorder, as determined by history, physical examination or laboratory testing. 3. Subjects with an unstable seizure disorder will be excluded. 4. Females with a positive urine pregnancy test. 5. Evidence of a prior adequate trial of aripiprazole (defined as a duration of greater than or equal to 2 weeks at a dose of at least 5 mg per day). When there is not evidence of a prior adequate trial of aripiprazole, subjects must be medication-free for at least 2 weeks prior to baseline. 6. Evidence of hypersensitivity to aripiprazole (defined as an allergic response \[e.g., skin rash\] or potentially serious adverse effect \[e.g., significant tachycardia\]). 7. History of neuroleptic malignant syndrome. 8. Subjects who, in the opinion of the investigator, are unsuitable in any other way to participate in this study including being unable to comply with the requirements of the study for any reason.

Design outcomes

Primary

MeasureTime frameDescription
Aberrant Behavior ChecklistObtained at Baseline and Week 12The Aberrant Behavior Checklist (ABC) is a 58-item measure of maladaptive behaviors and is used as a measure of drug effects. The ABC has 5 subscales: Social Withdrawal (16 items) ranging from 0 (not at all) to 48 (severe), Irritability (15 items) ranging from 0 (not at all) to 45 (severe), Inappropriate Speech (4 items) ranging from 0 (not at all) to 12 (severe), Hyperactivity (16 items) ranging from 0 (not at all) to 48 (severe), and Stereotypy (7 items) ranging from 0 (not at all) to 21 (severe). Items are rated from 0 (not at all) to 3 (severe).
Clinical Global Impressions- SeverityObtained at Baseline and Week 12The Clinical Global Impression - Severity scale (CGI-S) is a 7-point scale that requires the clinician to rate the severity of the patient's illness at the time of assessment, relative to the clinician's past experience with patients who have the same diagnosis. Considering total clinical experience, a patient is assessed on severity of mental illness at the time of rating 1, normal, not at all ill; 2, borderline mentally ill; 3, mildly ill; 4, moderately ill; 5, markedly ill; 6, severely ill; or 7, extremely ill.

Secondary

MeasureTime frameDescription
The Children's Yale-Brown Obsessive Compulsive ScaleObtained at Baseline and Week 12The CY-BOCS PDD has been utilized in a largescale clinical treatment study of repetitive behavior in idiopathic ASDs. CYBOCS-PDD scores range from 0 to 20 and measure repetitive/compulsive behavior and not obsessions. Higher score indicate worse outcome.
Social Responsiveness ScaleObtained at Baseline and Week 12The 65-item SRS is a standardized measure of the core symptoms of autism. Each item is scored on a 4-point Likert scale. The score of each individual item is summed to create a total raw score. A total scores results are as follows: 0-62: Within normal limits 63-79: Mild range of impairment 80-108: Moderate range of impairment 109-149: Severe range of impairment
The Vineland Adaptive Behavior ScalesScreen VisitVineland Adaptive Behavior Scales are a valid and reliable test to measure a person's adaptive level of functioning. Vineland-II forms aid in diagnosing and classifying intellectual and developmental disabilities and other disorders, such as autism spectrum disorders and developmental delays. The content and scales are organized within a 4 domain structure: Communication, Daily Living, Socialization and Motor Skills. The adaptive behavior composite standard score is computed from the sum of standard scores from the domains and converted into the adaptive behavior composite standard score. Higher scores indicate a higher adaptive level of functioning.
The Vineland Maladaptive Behavior SubscalesWeek 12The Vineland Adaptive Behavior Scales include an optional Maladaptive Behavior Index with 27 items. The Maladaptive Behavior Index is a composite of Internalizing, Externalizing, and other types of undesirable behavior that may interfere with the individual's adaptive functioning. The Maladaptive Behavior subscale yields raw scores (0-27).

Countries

United States

Participant flow

Participants by arm

ArmCount
Open-label Aripiprazole
Twelve subjects received open-label aripiprazole for 12 weeks. Mean dose, 9.8 mg/day
12
Total12

Baseline characteristics

CharacteristicOpen-label Aripiprazole
Aberrant Behavior Checklist
ABC Hyperactivity
31.8 units on a scale
STANDARD_DEVIATION 5.8
Aberrant Behavior Checklist
ABC Inappropriate Speech
6.8 units on a scale
STANDARD_DEVIATION 5.1
Aberrant Behavior Checklist
ABC Irritability S
25.3 units on a scale
STANDARD_DEVIATION 5.1
Aberrant Behavior Checklist
ABC Social Withdrawal
16.6 units on a scale
STANDARD_DEVIATION 11.8
Aberrant Behavior Checklist
ABC Stereotypy
12.7 units on a scale
STANDARD_DEVIATION 5.6
Age, Categorical
<=18 years
10 Participants
Age, Categorical
>=65 years
0 Participants
Age, Categorical
Between 18 and 65 years
2 Participants
Age, Continuous14.3 years
Children's Yale-Brown Obsessive Compulsive Scale Modified for PDD14.2 units on a scale
STANDARD_DEVIATION 4.6
Clinical Global Impressions - Severity4.5 units on a scale
STANDARD_DEVIATION 0.5
Region of Enrollment
United States
12 participants
Sex: Female, Male
Female
2 Participants
Sex: Female, Male
Male
10 Participants
Social Responsiveness Scale124.5 units on a scale
STANDARD_DEVIATION 26.7

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
— / —
other
Total, other adverse events
12 / 12
serious
Total, serious adverse events
0 / 12

Outcome results

Primary

Aberrant Behavior Checklist

The Aberrant Behavior Checklist (ABC) is a 58-item measure of maladaptive behaviors and is used as a measure of drug effects. The ABC has 5 subscales: Social Withdrawal (16 items) ranging from 0 (not at all) to 48 (severe), Irritability (15 items) ranging from 0 (not at all) to 45 (severe), Inappropriate Speech (4 items) ranging from 0 (not at all) to 12 (severe), Hyperactivity (16 items) ranging from 0 (not at all) to 48 (severe), and Stereotypy (7 items) ranging from 0 (not at all) to 21 (severe). Items are rated from 0 (not at all) to 3 (severe).

Time frame: Obtained at Baseline and Week 12

ArmMeasureGroupValue (MEAN)Dispersion
Open-label AripiprazoleAberrant Behavior ChecklistABC Hyperactivity15.6 units on a scaleStandard Deviation 8.1
Open-label AripiprazoleAberrant Behavior ChecklistABC Social Withdrawall9.6 units on a scaleStandard Deviation 10.7
Open-label AripiprazoleAberrant Behavior ChecklistABC Stereotypy7.6 units on a scaleStandard Deviation 5.6
Open-label AripiprazoleAberrant Behavior ChecklistABC Irritablity7.1 units on a scaleStandard Deviation 4.4
Open-label AripiprazoleAberrant Behavior ChecklistABC Inappropriate Speech4.0 units on a scaleStandard Deviation 3.2
Primary

Clinical Global Impressions- Severity

The Clinical Global Impression - Severity scale (CGI-S) is a 7-point scale that requires the clinician to rate the severity of the patient's illness at the time of assessment, relative to the clinician's past experience with patients who have the same diagnosis. Considering total clinical experience, a patient is assessed on severity of mental illness at the time of rating 1, normal, not at all ill; 2, borderline mentally ill; 3, mildly ill; 4, moderately ill; 5, markedly ill; 6, severely ill; or 7, extremely ill.

Time frame: Obtained at Baseline and Week 12

ArmMeasureValue (MEAN)Dispersion
Open-label AripiprazoleClinical Global Impressions- Severity3.5 units on a scaleStandard Deviation 0.5
Secondary

Social Responsiveness Scale

The 65-item SRS is a standardized measure of the core symptoms of autism. Each item is scored on a 4-point Likert scale. The score of each individual item is summed to create a total raw score. A total scores results are as follows: 0-62: Within normal limits 63-79: Mild range of impairment 80-108: Moderate range of impairment 109-149: Severe range of impairment

Time frame: Obtained at Baseline and Week 12

ArmMeasureValue (MEAN)Dispersion
Open-label AripiprazoleSocial Responsiveness Scale90.1 units on a scaleStandard Deviation 31.6
Secondary

The Children's Yale-Brown Obsessive Compulsive Scale

The CY-BOCS PDD has been utilized in a largescale clinical treatment study of repetitive behavior in idiopathic ASDs. CYBOCS-PDD scores range from 0 to 20 and measure repetitive/compulsive behavior and not obsessions. Higher score indicate worse outcome.

Time frame: Obtained at Baseline and Week 12

ArmMeasureValue (MEAN)Dispersion
Open-label AripiprazoleThe Children's Yale-Brown Obsessive Compulsive Scale10.6 units on a scaleStandard Deviation 5.7
Secondary

The Vineland Adaptive Behavior Scales

Vineland Adaptive Behavior Scales are a valid and reliable test to measure a person's adaptive level of functioning. Vineland-II forms aid in diagnosing and classifying intellectual and developmental disabilities and other disorders, such as autism spectrum disorders and developmental delays. The content and scales are organized within a 4 domain structure: Communication, Daily Living, Socialization and Motor Skills. The adaptive behavior composite standard score is computed from the sum of standard scores from the domains and converted into the adaptive behavior composite standard score. Higher scores indicate a higher adaptive level of functioning.

Time frame: Screen Visit

Population: Data for this outcome measure are unavailable because the data file was lost during a server migration.

Secondary

The Vineland Maladaptive Behavior Subscales

The Vineland Adaptive Behavior Scales include an optional Maladaptive Behavior Index with 27 items. The Maladaptive Behavior Index is a composite of Internalizing, Externalizing, and other types of undesirable behavior that may interfere with the individual's adaptive functioning. The Maladaptive Behavior subscale yields raw scores (0-27).

Time frame: Week 12

Population: Data for this outcome measure are unavailable because the data file was lost during a server migration.

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026