Overview

Study of Aripiprazole as an Adjunctive Therapy in Patients With Major Depressive Disorder

Status:
Completed
Trial end date:
2012-07-01
Target enrollment:
0
Participant gender:
All
Summary
To examine the efficacy and safety of aripiprazole versus placebo as an adjunctive therapy co-administered with either an selective serotonin reuptake inhibitor (SSRI) or a serotonin-norepinephrine reuptake inhibitor (SNRI) in patients with major depressive disorder.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Otsuka Pharmaceutical Co., Ltd.
Treatments:
Aripiprazole
Criteria
Inclusion Criteria:

1. Patients who are either inpatients or outpatients

2. Patients who 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

3. Patients diagnosed as having either "296.2x Major Depressive Disorder, Single Episode"
or "296.3x Major Depressive Disorder, Recurrent" according to DSM-IV-TR, and for whom
the current episode of major depressive disorder has been ongoing for more than 8
weeks

4. Patients with a HAM-D17 total score of 18 or more

Exclusion Criteria:

1. Female patients of child bearing potential who wish to become pregnant during the
treatment period, or within 4 weeks after study completion/discontinuation

2. Female patients who are pregnant, possibly pregnant, or breast feeding

3. Patients judged to be unable to tolerate any type of antidpressant treatment
(including drugs not being used in the current episode of major depressive disorder),
based on treatment history to date

4. Patients who have previously received electro-convulsive therapy

5. Patients who have participated in clinical studies on medical devices or other drugs
within the past month

6. Patients at risk of having serious adverse events or developing symptoms that could
interfere with safety and efficacy evaluations (such as symptoms of fibromyalgia
syndrome overlapping with symptoms of depression), based on previous medical history

7. Patients with a history or a complication of diabetes

8. Patients with thyroid disease (excluding patients who are stabilized on drug therapy
for at least 3 months)

9. Patients with a history of serotonin syndrome or psychotropic neuroleptic malignant
syndrome

10. Patients with a history of seizure disorder (epilepsy etc.)