Intramuscular Depot Formulation of Aripiprazole as Maintenance Treatment in Patients With Schizophrenia

Completed · Phase 3

Conditions studied: Schizophrenia

In brief

To evaluate the overall effectiveness of aripiprazole intramuscular (IM) depot as maintenance treatment in patients with schizophrenia.

Key facts

Study ID

NCT00731549

Run by

Otsuka Pharmaceutical Development & Commercialization, Inc.

People needed

1081

Starts

2008-12-01

Expected to finish

2013-11-01

Last updated by the study team

2014-11-26

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects who are able to provide written informed consent and/or consent obtained from a legally acceptable representative (as require by IRB/IEC), prior to the initiation of any protocol-required procedures.
• Male and female subjects 18 to 65 years of age, inclusive, at time of informed consent.
• Subjects who complete Studies 246/247 or who withdrew from the double-blind maintenance phase of either study (Phase 4 of Study 246 or Phase 3 of Study 247), or new subjects not participating in Studies 246/247.
• # Subjects who, in the investigator's judgment, require chronic treatment with an antipsychotic medication.
• Subjects able to understand the nature of the study and follow protocol requirements, including the prescribed dosage regimens, tablet ingestion, IM depot injection, discontinuation of prohibited concomitant medications, who can read and understand the written word in order to complete patient-reported outcomes measures, and who can be reliably rated on assessment scales.

You may not qualify if…

• Subjects with a current DSM-IV-TR diagnosis other than schizophrenia, including schizoaffective disorder, major depressive disorder, bipolar disorder, delirium, dementia, amnestic or other cognitive disorders. Also, subjects with borderline, paranoid, histrionic, schizotypal, schizoid or antisocial personality disorder.
• Subjects with schizophrenia that are considered resistant/refractory to antipsychotic treatment by history or response only to clozapine.
• Subjects with a significant risk of violent behavior or a significant risk of committing suicide based on history or investigator's judgment.
• Subjects who currently meet DSM-IV-TR criteria for substance dependence; including alcohol and benzodiazepines, but excluding caffeine and nicotine, or two positive drug screens for cocaine.
• Subjects who are known to be allergic, intolerant, or unresponsive to prior treatment with aripiprazole or other quinolinones.
• Subjects with a history of hypersensitivity to antipsychotic agents.
• Subjects with a history of neuroleptic malignant syndrome or clinically significant tardive dyskinesia at screening.

Where it is running

• Study site — Anaheim, California, United States
• Study site — Cerritos, California, United States
• Study site — Chino, California, United States
• Study site — Escondido, California, United States
• Study site — Garden Grove, California, United States
• Study site — Glendale, California, United States
• Study site — Glendale, California, United States
• Study site — Imperial, California, United States
• Study site — La Habra, California, United States
• Study site — Los Angeles, California, United States
• Study site — National City, California, United States
• Study site — Oceanside, California, United States
• Study site — Orange, California, United States
• Study site — Pasadena, California, United States
• Study site — Pico Rivera, California, United States
• Study site — San Bernardino, California, United States
• Study site — San Diego, California, United States
• Study site — San Diego, California, United States
• Study Site — San Diego, California, United States
• Study site — San Diego, California, United States
• Study site — Sherman Oaks, California, United States
• Study site — Torrance, California, United States
• Study site — Highlands Ranch, Colorado, United States
• Study site — Norwalk, Connecticut, United States
• Study site — Chandler, Arizona, United States

Full record on ClinicalTrials.gov

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