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CompletedNCT03292848Updated Jun 12, 2018

Trial to Assess the Pharmacokinetics, Safety, Tolerability of Oral Brexpiprazole in Children (6 to <13 Years Old) With Central Nervous System Disorders

A Phase 1 interventional study of Brexpiprazole in ADHD, Autism and Bipolar I Disorder, sponsored by Otsuka Pharmaceutical Development & Commercialization, Inc.. Completed at 9 sites in United States. Open to participants aged 6 Years to 12 Years. Per ClinicalTrials.gov, last updated 2018-06-12.

Sponsored by Otsuka Pharmaceutical Development & Commercialization, Inc. · Phase 1, Interventional, and Treatment

Phase
Phase 1
Study type
Interventional
Enrollment
24
Allocation
Non-randomized
Ages
6 Years to 12 Years
Sex
All
01

Study summary

A study to assess pharmacokinetics, safety and tolerability of brexpiprazole in children ages 6 to \<13 years with CNS disorders.

Read the detailed description

A US based nonrandomized, sequential cohort, crossover trial to assess pharmacokinetics, safety and tolerability of brexpiprazole in children ages 6 to \<13 years with CNS disorders who are receiving antipsychotic treatment for their medical condition.

02

Conditions studied

  • ADHD
  • Autism
  • Bipolar I Disorder
  • Conduct Disorder
  • Oppositional Defiant Disorder

Keywords

  • CNS Disorders
  • Brexpiprazole
03

Who can participate

Ages eligible
6 Years to 12 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Male and female subjects between 6 and 12 years of age
  • Subjects with CNS disorders including, but not limited to, ADHD, autism spectrum disorders, bipolar I disorder (subjects 10 to 12 years old only for bipolar), conduct disorder, oppositional defiant disorder, or any psychotic disorder and who are receiving antipsychotic treatment for their medical condition. Subjects' diagnoses will be determined by the Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM-5) criteria and confirmed at screening using the Kiddie Schedule for Affective Disorders and Schizophrenia-Present and Lifetime version (K-SADS-PL).
  • Subjects must be considered psychiatrically/medically appropriate for participation in a clinical trial in which they will receive two doses of an antipsychotic medication.
  • Subjects with good physical health, as determined by no clinically significant deviation from normal for all of the following, prior to enrollment in the trial:

    1. Medical history
    2. Clinical laboratory determination
    3. ECGs
    4. Physical examinations
  • Subjects who are within the 5th to 95th percentile for gender-specific BMI for age from the Centers for Disease Control and Prevention growth charts and weight at least 15 kg (approx. 33 lbs)
  • Ability to commit to remain fully abstinent or use 2 approved methods of birth control during the trial for 21 (± 2) days following the last dose of IMP for sexually active females of childbearing potential.
  • Ability, in the opinion of the PI, of the subject and the subject's legally acceptable representative or caregiver(s) to understand the nature of the trial and follow protocol requirements, including all of the following:

    1. Comply with prescribed dosage regimens and tablet ingestion, as well as the discontinuation of prohibited concomitant medications
    2. Reliably return for scheduled visits
    3. To be reliably rated on assessment scales

Exclusion criteria

Exclusion Criteria:

  • Subjects with a clinical presentation or history that is consistent with delirium, dementia, amnesia, or other cognitive disorders; subjects with psychotic symptoms that are better accounted for by another general medical condition(s) other than those listed in the second inclusion criterion above, or direct effect of a substance (ie, medication, illicit drug use, etc.).
  • Subjects with a history of at least mild intellectual disability as determined by IQ \< 70, clinical evidence, or a social or school history that is suggestive of intellectual disability.
  • Subjects who have any of the following:

    1. A significant risk of committing suicide based on history and the principal investigator's clinical judgment, or routine psychiatric status examination
    2. Current suicidal behavior
    3. Imminent risk of injury; active suicidal ideation
    4. Any lifetime history of suicidal behavior detected by the Children's Baseline/Screening version of the C-SSRS.
  • Subjects with a lifetime history of a substance use disorder (as determined by the DSM-5 criteria), or current substance misuse including alcohol and benzodiazepines, but excluding caffeine and nicotine.
  • Subjects who currently have clinically significant neurological, hepatic, renal, metabolic, hematological, immunological, cardiovascular, pulmonary, or gastrointestinal disorders such as any history of myocardial infarction, congestive heart failure, HIV seropositive status/acquired immunodeficiency syndrome, or chronic hepatitis B or C. Medical conditions that are minor or well-controlled may be considered acceptable if the condition does not expose the subject to an undue risk of significant adverse event or interfere with assessments during the course of the trial.
  • Subjects with insulin dependent diabetes mellitus (IDDM) are excluded. Subjects with non-IDDM may be eligible for the trial if their condition is determined to be stable.
  • Subjects with epilepsy or a history of seizures (except for a single seizure episode, for instance childhood febrile seizure or post traumatic) or a history of severe head trauma or cerebrovascular disease (eg, stroke, transient ischemic attack, etc.).
  • Any major surgery within 30 days prior to the first dose of IMP.
  • Any history of significant bleeding or hemorrhagic tendencies.
  • Blood transfusions within 30 days prior to first dose of IMP.
  • Subjects with a positive drug screen for cocaine, marijuana (even if by prescription), or other illicit drugs, or alcohol are excluded and may not be retested or rescreened.
  • Subjects who have supine or standing diastolic blood pressure, after resting for at least 5 minutes, ≥ 95 mmHg.
  • Subjects who have had a dose of depot antipsychotics within 6 months of screening.
  • Consumption of alcohol or grapefruit, grapefruit juice, Seville oranges, or Seville orange juice within 72 hours prior to the first dose of IMP and throughout the trial
  • Subjects who participated in a clinical trial and were exposed to IMP within the last 30 days prior to screening or who participated in more than 2 interventional clinical trials within the past year.
  • Subjects with a history of neuroleptic malignant syndrome or hypersensitivity to atypical antipsychotics.
  • Subjects with a history of true allergic (i.e. not intolerance) response to more than one class of medications.
  • Subjects with a history of allergic reaction or a known or suspected sensitivity to any substance that is contained in the IMP formula.
  • Subjects who do not tolerate venipuncture or have poor venous access that would cause difficulty for collecting blood samples.
  • Prisoners or subjects who are compulsorily detained (e.g. juvenile detention, court-mandated treatment) for any reason.
  • Inability to tolerate oral medication or swallow tablets.
04

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
24 participants (actual)

Study arms

  • Experimental
    10 to <13 Years of Age

    Two doses will be administered with a washout period of 14 days between the first dose of 1.5 mg the second dose of 3 mg.

    Drug: Brexpiprazole

  • Experimental
    6 to <10 Years of Age

    Two doses will be administered with a washout period of 14 days between the first dose of 0.75 mg and the second dose of 1.5 mg.

    Drug: Brexpiprazole

Interventions

  • DrugBrexpiprazole

    Tablet

    Also known as: OPC-34712

05

What researchers measure

Primary outcomes

  1. Maximum Plasma Concentration (Cmax) [PK]

    The maximum plasma concentration of drug will be assessed for brexpiprazole and its major metabolite DM-3411.

    Time frame: Up to 22 days or early termination

  2. Area under concentration-time curve (AUC) calculated from time zero to time t (AUCt) [PK]

    AUCt will be assessed for plasma brexpiprazole and its major metabolite DM-3411 to determine average concentration of drug over time

    Time frame: Up to 22 days or early termination

  3. AUC from time zero to infinity [PK]

    AUC infinity will be assessed for plasma brexpiprazole and its major metabolite DM-3411 to determine total drug exposure over time

    Time frame: Up to 22 days or early termination

  4. Time of maximum plasma concentration (tmax) [PK]

    The amount of time that the maximum plasma concentration of drug will be assessed for plasma brexpiprazole and its major metabolite DM-3411

    Time frame: Up to 22 days or early termination

  5. Terminal-phase elimination half-life (t½,z) [PK]

    t½,z will be assessed for plasma brexpiprazole and its major metabolite DM-3411 to determine drug persistence in the body

    Time frame: Up to 22 days or early termination

  6. Apparent clearance of drug from plasma after extravascular administration (CL/F) [PK]

    CL/F for brexpiprazole only

    Time frame: Up to 22 days or early termination

Secondary outcomes

  1. Treatment-Emergent Adverse Events (TEAES) [Safety]

    Time frame: Up to 22 days or early termination with a 21 day follow-up period

  2. Clinical laboratory tests [Safety]

    Collect hematology, serum chemistry,and urinalysis will be assessed to determine the safety and tolerability of drug

    Time frame: Up to 22 days or early termination

  3. Vital signs observed and change from baseline data (systolic and diastolic blood pressure) [Safety]

    Time frame: Up to 22 days or early termination

  4. Vital signs observed and change from baseline data (heart rate) [Safety]

    Time frame: Up to 22 days or early termination

  5. Vital signs observed and change from baseline data (respiratory rate) [Safety]

    Time frame: Up to 22 days or early termination

  6. Vital signs observed and change from baseline data (body temperature) [Safety]

    Time frame: Up to 22 days or early termination

  7. 12-lead electrocardiogram (ECGs) [Safety]

    Time frame: Up to 22 days or early termination

  8. Physical examinations (height) [Safety]

    Height is measured in cm,and will be used to calculate Body Mass Index (BMI)

    Time frame: Up to 22 days or early termination

  9. Physical examinations (weight) [Safety]

    Weight is measured in kg, and will be used to calculate Body Mass Index (BMI)

    Time frame: Up to 22 days or early termination

  10. Physical examinations- Body Mass Index (BMI) [Safety]

    Body Mass Index (BMI) measured using height (cm) and weight (kg)

    Time frame: Up to 22 days or early termination

  11. Physical examinations- review of body systems [Safety]

    Subject will be examined by site staff for any notable changes

    Time frame: Up to 22 days or early termination

  12. Simpson-Angus Scale (SAS) rating scale [Safety]

    Will be used in analysis of Extrapyramidal Symptoms (EPS)

    Time frame: Up to 22 days or early termination

  13. Abnormal Involuntary Movement Scale (AIMS) [Safety]

    Will be used in analysis of Extrapyramidal Symptoms (EPS)

    Time frame: Up to 22 days or early termination

  14. Barnes Akathisia Rating Scale (BARS) [Safety]

    Will be used in analysis of Extrapyramidal Symptoms (EPS)

    Time frame: Up to 22 days or early termination

  15. Columbia-Suicide Severity Rating Scale (C-SSRS) [Safety]

    Time frame: Up to 22 days or early termination

06

Study locations

9 sites
  • Woodland International Research Group
    Little Rock, Arkansas 72211, United States
  • Woodland Research Northwest, LLC
    Rogers, Arkansas 72758, United States
  • Alliance for Wellness dba Alliance for Research
    Long Beach, California 90807, United States
  • New Hope Clinical Research
    Charlotte, North Carolina 28211, United States
  • IPS Research Company
    Oklahoma City, Oklahoma 73103, United States
  • Cutting Edge Research Group
    Oklahoma City, Oklahoma 73116, United States
  • Clinical Trials of Texas, Inc.
    San Antonio, Texas 78229, United States
  • Road Runner Research Ltd.
    San Antonio, Texas 78249, United States
  • Aspen Clinical Research
    Orem, Utah 84058, United States
07

Registry details

Key details

Study ID
NCT03292848
Lead sponsor
Otsuka Pharmaceutical Development & Commercialization, Inc.
Collaborators
H. Lundbeck A/S
Responsible party
Sponsor
First posted
Sep 26, 2017
Start date
Oct 10, 2017
Primary completion
May 21, 2018
Completion
May 21, 2018
Last update
Jun 12, 2018

Oversight

FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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