Overview

A Multicenter, Investigative Study of the Safety and Efficacy of Extended Administration of Aripiprazole in Combination With Mood Stabilizer for the Treatment of Patients With Bipolar Disorder Experiencing a Manic or Mixed Episode

Status:
Completed
Trial end date:
2010-11-01
Target enrollment:
0
Participant gender:
All
Summary
To assess the safety and efficacy of long-term administration of aripiprazole by performing extended administration of aripiprazole in combination with mood stabilizer (lithium or valproate) in an unblinded manner to those patients who completed the preceding multicenter, double-blind, placebo-controlled, parallel group-comparison trial of aripiprazole in patients with bipolar disorder experiencing a manic or mixed episode (Study 031-06-003, hereafter "Study 003") but whose condition worsened or remained unchanged or who discontinued Study 003 between Day 14 and Day 21 due to lack of drug efficacy.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Otsuka Pharmaceutical Co., Ltd.
Treatments:
Aripiprazole
Criteria
Inclusion Criteria:

- Trial subjects will be men and women of age 18 or above and below the age of 65 who
will not be turning 65 during the trial.

- Subjects have the ability to understand and to provide informed consent to the
examination, observation, and evaluation processes specified in this protocol, and
have signed the informed consent form based on a full understanding of the trial.

- Subjects who meet DSM-IV-TR criteria for manic or mixed episodes and have been
diagnosed as having "296.4x Bipolar I Disorder in which the most recent episode was
manic" or "296.6x Bipolar I Disorder in which the most recent episode was mixed"

- Subjects who were enrolled in and have completed or withdrawn from Study 003 and who
meet the following criteria

- Subjects who show exacerbation of condition or no change in condition: Those
subjects who completed Study 003, and whose score for CGI-BP Change from
preceding phase (mania) on Day 21 (completion of Study 003) was between 5
(Minimally worse) and 7 (Very much worse) (subjects showing exacerbation of
condition), or whose score was 4 (No change) (subjects showing no change in
condition)

- Subjects who discontinued due to lack of drug efficacy: Those subjects who
discontinued Study 003 between Day 14 and Day 21, for whom the reason of
withdrawal was lack of drug efficacy, and whose score for CGI-BP Change from
preceding phase (mania) was between 5 (Minimally worse) and 7 (Very much worse)

Exclusion Criteria:

- Subjects presenting with a clinical picture and/or history that is consistent with a
DSM-IV-TR diagnosis of:

- Delirium, dementia, amnestic disorder, or other cognitive disorders

- Schizophrenia or other psychotic disorder

- Personality disorder

- Subjects with psychotic symptoms that are clearly due to another general medical
condition or direct physiological effects of a substance

- Subjects who represent a significant risk of committing suicide

- Subjects known to have a complication of allergy to aripiprazole, other
quinolinone-skeleton compounds, lithium, or valproate

- Subjects with a complication of neuroleptic malignant syndrome

- Subjects in a state of physical exhaustion accompanied by such conditions as
dehydration or malnutrition

- Subjects with a complication of paralytic ileus

- Subjects with a complication of organic brain disorder or convulsive disorder, such as
epilepsy

- Subjects with a complication of diabetes