Brexpiprazole (OPC-34712) as an Adjunctive Treatment in Active Adults, 18 to 35 Years Old, With Major Depressive Disorder Who Are in a School or Work Environment
Status: | Completed |
---|---|
Conditions: | Depression, Depression, Major Depression Disorder (MDD) |
Therapuetic Areas: | Psychiatry / Psychology, Pulmonary / Respiratory Diseases |
Healthy: | No |
Age Range: | 18 - 35 |
Updated: | 4/21/2016 |
Start Date: | November 2013 |
End Date: | October 2014 |
Protocol 331-13-003: An Exploratory, Multicenter, Open-label, Flexible-dose Trial of Brexpiprazole (OPC 34712) as an Adjunctive Treatment in Active Adults, 18 to 35 Years Old, With Major Depressive Disorder Who Are in a School or Work Environment.
To investigate the efficacy and safety of flexibly dosed adjunctive brexpiprazole treatment
in active adults with MDD, 18 to 35 years old, who are experiencing an inadequate selective
serotonin reuptake inhibitor (SSRI)/serotonin norepinephrine reuptake inhibitor (SNRI)
response in a school or work environment.
in active adults with MDD, 18 to 35 years old, who are experiencing an inadequate selective
serotonin reuptake inhibitor (SSRI)/serotonin norepinephrine reuptake inhibitor (SNRI)
response in a school or work environment.
Main Inclusion Criteria:
Have a diagnosis of a single or recurrent, nonpsychotic episode of MDD as defined by the
Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision
(DSM-IV-TR) and confirmed by both the Mini International Neuropsychiatric Interview
(M.I.N.I.) and an adequate clinical psychiatric evaluation.
Have a treatment history of an inadequate ADT response to at least 1 ADT (but not > 3) for
the current episode.
Have received a single, trial-approved, SSRI or SNRI at an adequate dose for ≥ 6 weeks
prior to screening.
Are 18 to 35 years old at the time of consent (inclusive, and outpatients only).
Are (and will be) working 20 hours or more per week or a student taking 6 credit hours or
more during the trial period, however minor deviations from the "part-time" concept may be
acceptable on a case-by-case basis based on approval of the medical monitor.
Have a Hamilton Depression Rating Scale (HAM-D)- 17-item Total Score ≥ 18 at screening and
baseline.
Have a Sheehan Disability Scale (SDS) 3-item mean score ≥ 5 at baseline.
Main Exclusion Criteria:
Subjects with any of the following current Axis I DSM-IV-TR diagnoses: delirium, dementia,
amnestic, or other cognitive disorders; schizophrenia, schizoaffective disorder, or other
psychotic disorders; bipolar I disorder, bipolar II disorder, or bipolar disorder not
otherwise specified (NOS); eating disorders (including anorexia nervosa or bulimia);
obsessive compulsive disorder; panic disorder; post-traumatic stress disorder; and
attention deficit hyperactivity disorder.
Subjects with any of the following current Axis II DSM-IV-TR diagnoses: borderline,
antisocial, paranoid, schizoid, schizotypal or histrionic personality disorders, or mental
retardation.
We found this trial at
24
sites
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