Status:
TERMINATED
Adaptive Phase II Study to Evaluate the Safety & Efficacy of NaBen®
Lead Sponsor:
SyneuRx International (Taiwan) Corp
Conditions:
Schizophrenia
Eligibility:
All Genders
12-17 years
Phase:
PHASE2
PHASE3
Brief Summary
The purpose of this study is to determine if NaBen® is a safe and effective add-on treatment for schizophrenia in adolescents.
Detailed Description
This is a two-part, multi-center, prospective, randomized, placebo-controlled, parallel-group study, in which adolescent subjects with schizophrenia will be enrolled. Overall, eligible subjects will b...
Eligibility Criteria
Inclusion
- Male or female subjects who are between 12 and 17 years of age inclusive
- Physician confirmed DSM-IV or -V diagnosis of schizophrenia based on MINI International Neuropsychiatric Interview for Schizophrenia and Psychotic Disorders Studies for Children and Adolescents, version 6.0 (MINI-KID, Version 6.0)
- Are clinically stable with residual symptoms, defined as a total score of ≥ 60 of PANSS and a score of ≥ 40 for SANS
- An unchanged antipsychotic medication regimen for at least eight (8) weeks prior to randomization into the study and expected to remain unchanged during the study (longer for depot or long-acting antipsychotics: ten (10) months for Aripiprazole (Maintena®) and Paliperidone (Xeplion®); six (6) months for Olanzapine pamoate monohydrate (Zypadhera®); and at least 6 times duration of the reported half life or minimum four (4) months for other depot or long-acting antipsychotics)
- In good general physical health and all physical exam, neurological exam and laboratory assessments (urine/blood routine, biochemical tests and ECG) are clinically unremarkable per the investigator
- Subject has a negative urine illicit drug screening test
- Subject understands and is willing to sign the Informed Assent Form (IAF) prior to study entry and agrees to be available for all the study visits
- The subject's guardian understands and is willing to sign the Informed Consent Form (ICF) prior to study entry and agrees to be available for all the study visits
- Must not be a danger to self or others and must have family support available to be maintained as outpatients
Exclusion
- Meets the DSM-IV or -V criteria at screening for mental retardation, dissociative disorder, bipolar disorder, major depressive disorder, schizoaffective disorder, schizophreniform disorder, autistic disorder, or primary substance induced psychotic disorder. Other comorbid disorders; e.g., attention-deficit hyperactivity disorder (ADHD), are allowed as long as schizophrenia is the primary diagnosis and the comorbid disorder(s) do not require medication.
- Subjects whose illness was resistant to antipsychotics according to prior trials of two different antipsychotics of adequate dose
- History of epilepsy, head trauma, or neurological illness other than Tourette's syndrome
- History of allergic reaction to sodium benzoate
- Serious medical illnesses such as acute or chronic renal disease, liver failure or heart disease that, in the opinion of the investigator, may interfere with the conduct of the study.
- Current substance abuse or positive urine illicit drug screening or history of substance dependence (including alcohol, but excluding nicotine and caffeine) in the past three (3) months.
- Use of depot antipsychotics in the past six (6) months
- Inability to follow protocol
- Body Mass Index (BMI) \> 35
- Female subjects who are pregnant (as confirmed by urine pregnancy test performed at screening Visit) or are nursing, or who do not agree to abstinence or birth control during the study
- Cancer within the last three (3) years except for basal cell carcinoma and squamous cell carcinoma
- Previous participation in an intervention trial within 30 days of randomization
- Subjects whose PANSS score has decreased more than 10 percent during the Screening Phase
Key Trial Info
Start Date :
June 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 26 2023
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT01908192
Start Date
June 1 2014
End Date
October 26 2023
Last Update
May 9 2024
Active Locations (23)
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1
Harmonex Neuroscience Research
Dothan, Alabama, United States, 36303
2
CiTrials
Bellflower, California, United States, 90706
3
Renew Behavioral Health, Inc.
Long Beach, California, United States, 90807
4
CiTrials
Riverside, California, United States, 92506