Status:
COMPLETED
A Multicenter Open-label Study Investigating the Pharmacokinetics and Safety of Aripiprazole IM Depot Formulation (OPC-14597 IMD) During Repeated Administration by Injection Into the Deltoid Muscle in Patients With Schizophrenia
Lead Sponsor:
Otsuka Pharmaceutical Co., Ltd.
Conditions:
Schizophrenia
Eligibility:
All Genders
18-64 years
Phase:
PHASE1
Brief Summary
To assess the pharmacokinetics and safety of aripiprazole intra-muscular (IM) depot formulation in patients with schizophrenia after repeated administration by injection into the deltoid muscle for a ...
Eligibility Criteria
Inclusion
- Patients with a diagnosis of schizophrenia as defined by Diagnostic and Statistical Manual (DSM)-IV-Text Revision (TR) (295.30, 295.10, 295.20, 295.90, 295.60)
- Patients who have provided written informed consent by themselves (If the patient is a minor, written consent from a legal representative must be obtained in addition to the patient's own written informed consent.)
- Patients, both male and female, aged 18 years or older, but younger than 65 years, at the time of obtaining informed consent
- Patients with a body mass index of 18.5 or higher and lower than 35.0
- Patients whose mental condition is stable or well maintained for 2 weeks or more without any change to dosage regimen for their non-aripiprazole oral atypical antipsychotic monotherapy prior to obtaining informed consent
- Patients who have received aripiprazole in the past
Exclusion
- Patients diagnosed as having a mental disorder other than schizophrenia, as defined by DSM-IV-TR criteria.
- Patients with a history or complication of diabetes.
- Patients with hepatic, renal, cardiac, or hematopoietic disorders.
- Female patients who are pregnant or lactating, who may possibly be pregnant, who wish to become pregnant, or male patients whose partner wishes to become pregnant.
- Patients who have a drug allergy or drug hypersensitivity
- Patients for whom clozapine has been ineffective, patients who have responded only to clozapine, or patients who are currently being treated with clozapine.
- Patients with a complication of Parkinson's Disease (excluding drug-induced Parkinsonism).
- Patients with a history or a complication of neuroleptic malignant syndrome, rhabdomyolysis, tardive dyskinesia, paralytic ileus or water intoxication.
- Patients with a history or a complication of psychological or behavioral abnormalities associated with use of psychoactive substances (abuse of alcohol, narcotics, or organic solvent, etc).
- Patients with a history or a complication of suicide attempt or self-injury within 52 weeks prior to obtaining informed consent.
- Patients with a history of or a complication of convulsive disorder such as epilepsy.
- Patients with a history of or a complication of organic brain disorder including cerebrovascular disease.
- Patients with a history or a complication of granulocytopenia or agranulocytosis.
- Patients who have received electro-convulsive therapy (ECT) within 12 weeks prior to obtaining informed consent.
Key Trial Info
Start Date :
July 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 1 2015
Estimated Enrollment :
17 Patients enrolled
Trial Details
Trial ID
NCT02220712
Start Date
July 1 2014
End Date
April 1 2015
Last Update
January 25 2021
Active Locations (5)
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1
Chugoku Region, Japan
2
Hokkaido Region, Japan
3
Kanto Region, Japan
4
Kinki Region, Japan