A Trial to Assess the Pharmacokinetics, Safety, and Tolerability of Centanafadine in Pediatric Subjects With Attention-deficit/Hyperactivity Disorder

Study Identifier:

405-201-00010

ClinicalTrials.gov Identifier:

NCT04398225

EudraCT Identifier:

N/A

EU CT ID:

N/A

Study Contact Information:

N/A

Study Complete

Subscribe to Updates

Study Details

Medical Condition

ADHD

Study Drug

Drug: Centanafadine

Date

Jun 2020 - Apr 2021

Phase 1/2

Phase 2/3

Phase 1

Phase 2

Phase 3

Phase 4

N/A

Patient Requirements

Sex: Female & Male

Age: 4 - 12 Years

Requirements Information

Inclusion and Exclusion Criteria

Inclusion Criteria

Male or female subjects 4 to 12 years of age, inclusive, at the time of informed consent/assent.
Subjects must weight ≥ 13 kg.
Subjects with a diagnosis of any ADHD subtype based on Diagnostic and Statistical Manual of Mental Disorders, 5th edition (DSM-5) criteria and confirmed by the Mini-International Neuropsychiatric Interview for Children and Adolescents (MINI-Kid).
Subject is judged by the investigator to be clinically stable, and has not had any psychiatric hospitalizations within the past 12 weeks.
Subjects and their caregivers must be able and willing to utilize the AiCure Platform for each daily dose.

Exclusion Criteria

Subjects with a clinical presentation or history that is consistent with delirium, dementia, amnesia, or other cognitive disorders; subjects with psychiatric symptoms that are better accounted for by another psychiatric or general medical condition(s) or direct effect of a substance.
Subjects with developmental disorders, such as Autism Spectrum Disorder.
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 with hypothyroidism or hyperthyroidism (unless condition has been stabilized with medications for at least 90 days prior to first dose of IMP) or an abnormal result for free T4 at screening.
Subjects who currently have clinically significant neurological, dermatological, hepatic, renal, metabolic, hematological, immunological, cardiovascular, pulmonary, or gastrointestinal disorders such as any history of myocardial infarction, congestive heart failure, HIV seropositive status/AIDS, or chronic hepatitis B or C.
Subjects with insulin dependent diabetes mellitus (i.e. any subjects using insulin)
Subjects with epilepsy, Tourette's Disorder, or a history of seizures or a history of severe head trauma or cerebrovascular disease.
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 the first dose of IMP.
Subjects who have supine or standing diastolic blood pressure, after resting for at least 5 minutes, \> 80 mmHg.
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 who have had any previous exposure to centanafadine.
Subjects with a history of true allergic response to a medication or a history of dermatologic adverse reactions or anaphylaxis secondary drug exposure.
Subjects with a history of allergic reaction or known or suspected sensitivity to any substance that is contained in the IMP formulation.
Subjects who do not tolerate venipuncture or have poor venous access that would cause difficulty for collecting blood samples.
Consumption of alcohol and/or food and beverages containing methylxanthines, foods known to affect CYP1A2 (e.g. charbroiled or pan-fried meats and cruciferous vegetables) within 72 hours prior to dosing.
Relative of the trial site employees cannot participate in the trial.
Siblings, other family members, and those having the same place of residence as the subject are also excluded from the trial.

Protocol Summary

This trial will evaluate the pharmacokinetics, safety, and tolerability of centanafadine in pediatric subjects with ADHD.

Study Locations

Location

Status

Location

For additional information regarding sites, contact 844-687-8522

Hollywood, Florida, United States, 33024

Status

N/A

July 2025 01US25EUC0279

Requirements information

Inclusion criteria

Male or female subjects 4 to 12 years of age, inclusive, at the time of informed consent/assent.
Subjects must weight ≥ 13 kg.
Subjects with a diagnosis of any ADHD subtype based on Diagnostic and Statistical Manual of Mental Disorders, 5th edition (DSM-5) criteria and confirmed by the Mini-International Neuropsychiatric Interview for Children and Adolescents (MINI-Kid).
Subject is judged by the investigator to be clinically stable, and has not had any psychiatric hospitalizations within the past 12 weeks.
Subjects and their caregivers must be able and willing to utilize the AiCure Platform for each daily dose.

Exclusion criteria

Subjects with a clinical presentation or history that is consistent with delirium, dementia, amnesia, or other cognitive disorders; subjects with psychiatric symptoms that are better accounted for by another psychiatric or general medical condition(s) or direct effect of a substance.
Subjects with developmental disorders, such as Autism Spectrum Disorder.
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 with hypothyroidism or hyperthyroidism (unless condition has been stabilized with medications for at least 90 days prior to first dose of IMP) or an abnormal result for free T4 at screening.
Subjects who currently have clinically significant neurological, dermatological, hepatic, renal, metabolic, hematological, immunological, cardiovascular, pulmonary, or gastrointestinal disorders such as any history of myocardial infarction, congestive heart failure, HIV seropositive status/AIDS, or chronic hepatitis B or C.
Subjects with insulin dependent diabetes mellitus (i.e. any subjects using insulin)
Subjects with epilepsy, Tourette's Disorder, or a history of seizures or a history of severe head trauma or cerebrovascular disease.
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 the first dose of IMP.
Subjects who have supine or standing diastolic blood pressure, after resting for at least 5 minutes, \> 80 mmHg.
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 who have had any previous exposure to centanafadine.
Subjects with a history of true allergic response to a medication or a history of dermatologic adverse reactions or anaphylaxis secondary drug exposure.
Subjects with a history of allergic reaction or known or suspected sensitivity to any substance that is contained in the IMP formulation.
Subjects who do not tolerate venipuncture or have poor venous access that would cause difficulty for collecting blood samples.
Consumption of alcohol and/or food and beverages containing methylxanthines, foods known to affect CYP1A2 (e.g. charbroiled or pan-fried meats and cruciferous vegetables) within 72 hours prior to dosing.
Relative of the trial site employees cannot participate in the trial.
Siblings, other family members, and those having the same place of residence as the subject are also excluded from the trial.

A Trial to Assess the Pharmacokinetics, Safety, and Tolerability of Centanafadine in Pediatric Subjects With Attention-deficit/Hyperactivity Disorder

Study Details

Protocol Summary

Study Locations

© 2025 Otsuka America Pharmaceutical,

Inc All rights reserved.

July 2025 01US25EUC0279