VA Augmentation and Switching Treatments for Improving Depression Outcomes

The overall aim of VAST-D is to enhance treatment outcomes for representative outpatients
diagnosed with nonpsychotic major depressive disorder (MDD) and treated in primary or
psychiatric VA care settings. In particular, VAST-D is designed to determine the comparative
effectiveness of different treatment options for participants with MDD who fail to have a
satisfactory outcome to treatment with their initial antidepressants.

These options may be conceptualized as representing two overall treatment strategies: 1)
Medication Switch - switching from the initial antidepressant to another antidepressant
medication, specifically bupropion-SR and 2) Medication Augmentation - augmenting the initial
antidepressant with a second antidepressant, specifically bupropion-SR or a second generation
antipsychotic, specifically aripiprazole. VAST-D's primary goal is to determine which of
these 3 treatment strategies is most likely to lead to remission. Other key objectives
include comparisons of response, time to remission, time to response, relapse, anxiety
symptoms, suicidal ideation and behaviors, side effects, tolerability, quality of life,
health related costs and satisfaction with participation in the study.

VAST-D will enroll 1518 total patients of both genders and all ethnic/racial and
socioeconomic backgrounds. All patients will meet Diagnostic and Statistical Manual of Mental
Disorders (DSM)-IV-TR (text revised) criteria for nonpsychotic MDD. The diagnostic criteria
for eligibility will be established by clinical interview supplemented with the 9-item
Patient Health Questionnaire (PHQ-9). Final determination for eligibility will be made by the
study clinician. Only participants with a suboptimal outcome to a well documented, adequately
delivered (dose and duration), trial with selective serotonin reuptake inhibitor (SSRI) or a
serotonin and norepinephrine reuptake inhibitor (SNRI) or mirtazapine will be eligible for
the study. Failure to achieve an adequate outcome will be ascertained by a score on the
16-item Quick Inventory of Depressive Symptomatology - Clinician rated (QIDS-C16) scale >= 16
(considered severe depression) after at least 6 weeks of treatment or QIDS-C16 >= 11
(considered moderately severe depression) after at least 8 weeks of treatment. Otherwise, the
inclusion criteria are broad and the exclusion criteria are few; participants with most
comorbid general medical or psychiatric disorders are generally included to provide a broadly
representative sample.

Participants will be randomized (1:1:1 ratio) to switch to bupropion-SR alone (n=506),
current antidepressant plus bupropion-SR (n=506), or current antidepressant plus aripiprazole
(n=506). Treatment will be guided by clinician-rated symptom measures (the PHQ-9) and global
side effects measures (the Frequency, Intensity, and Burden of Side Effects Rating or FIBSER)
obtained at each treatment visit. Acute treatment visits will occur at baseline and at weeks
1, 2, 4, 6, 8, 10, and 12 to ensure delivery of appropriate and yet vigorous and tolerable
pharmacotherapy. Participants who tolerate the acute treatment and achieve adequate response
at 12 weeks will enter the 24-week Continuation Treatment phase, during which the initial
treatment will continue and visits will occur every four weeks subsequently until patients
have been followed for 36 weeks post-randomization. The QIDS-C16 will be administered at
baseline and at each follow-up visit by an independent evaluator (who will be blinded to
treatment assignment) to measure symptoms of depression for the study outcomes of remission,
response and relapse. Neither the participant nor the treating clinician will be blinded to
treatment.

Primary hypotheses:

Primary hypothesis 1.a: Remission rate from major depressive disorder will be higher in
patients whose treatment is augmented with bupropion-SR (antidepressant + bupropion-SR)
compared to those switched to bupropion-SR monotherapy.

Primary Hypothesis 1.b: Remission rate from major depressive disorder will be higher in
patients whose treatment is augmented with aripiprazole (antidepressant + aripiprazole)
compared to those switched to bupropion-SR monotherapy.

Secondary hypotheses:

Secondary Hypothesis 2.a: Remission rate will be greater in patients whose treatment is
augmented with bupropion-SR (antidepressant + bupropion-SR) than in those augmented with
aripiprazole (antidepressant + aripiprazole).

Secondary Hypothesis 2.b: Relapse rate (within 36 weeks of the initiation of treatment) will
be lower in patients whose antidepressant is augmented with bupropion-SR (antidepressant +
bupropion-SR) than in those whose antidepressant is switched to bupropion-SR monotherapy.

Secondary Hypothesis 2.c: Relapse rate (within 36 weeks of the initiation of treatment) will
be lower in patients whose treatment is augmented with aripiprazole (antidepressant +
aripiprazole) vs. those switched to bupropion-SR monotherapy.

Secondary Hypothesis 2.d: Relapse rate (within 36 weeks of the initiation of treatment) will
be lower in patients whose treatment is augmented with bupropion-SR (antidepressant +
bupropion-SR) than in patients whose treatment was augmented with aripiprazole
(antidepressant + aripiprazole).

Secondary Hypothesis 2.e: The proportion of patients who develop akathisia, other
akathisia-like side effects (e.g., tremor, irritability, motor restlessness) and
extrapyramidal side effects will be greater in the patients whose antidepressant treatment is
augmented with aripiprazole (antidepressant + aripiprazole) compared to patients whose
treatment is augmented with bupropion-SR (antidepressant + bupropion-SR), or switched to
bupropion-SR monotherapy.

Secondary Hypothesis 2.f: The relative costs (direct and indirect) of augmenting an
antidepressant with aripiprazole (antidepressant + aripiprazole) will be greater than the
costs of antidepressant augmentation with bupropion-SR (antidepressant + bupropion-SR), and
the costs of antidepressant augmentation with bupropion-SR (antidepressant + bupropion-SR)
will be greater than the costs of switching to bupropion-SR monotherapy, and augmentation and
monotherapy with bupropion-SR will be more cost-effective than aripiprazole augmentation.

Inclusion Criteria:

- DSM-IV diagnosis of single or recurrent, non-psychotic, major depressive disorder

- Currently taking a selective serotonin reuptake inhibitor (SSRI) or
serotonin-norepinephrine reuptake inhibitor (SNRI) or mirtazapine for major depressive
disorder

- Need for "next-step" treatment based on documented suboptimal outcome from current
antidepressant treatment for major depressive episode (at least 6 weeks treatment with
a QIDS-C16 >= 16 or at least 8 weeks with a QIDS-C16 >= 11; and at least 3 weeks at a
stable "optimal" dose

- Age: 18 years of age or older

Exclusion Criteria:

- Prior inadequate response after an adequate treatment trial or clear cut intolerance
to either of the study medications (aripiprazole or bupropion)

- Current treatment with bupropion, aripiprazole or any other antipsychotic agent

- Lifetime history of bipolar disorder, schizophrenia, schizoaffective disorder, or
psychosis not otherwise specified

- Current diagnosis of Dementia

- Current diagnosis of an eating disorder or a seizure disorder

- High suicide risk currently requiring acute intervention (other than outpatient
treatment of depression)

- Unstable, serious medical condition or one requiring acute medical treatment, or
anticipation of hospitalization for extended care

- Requiring immediate hospitalization for psychiatric disorders

- Physiologic substance dependence requiring detoxification (excluding nicotine) in the
past 30 days (substance abuse is not an exclusion criteria)

- Taking any concomitant medication that contraindicates any of treatment options or
augmenting agents known to have an antidepressant effect

- Concurrent or recent participation (within the last 30 days) in another conflicting
clinical trial with a mental health, investigational drug, or medical device
intervention

- Female - pregnant or lactating or planning to become pregnant

- Patient was not able or willing to provide informed consent; or changed mind about
participating prior to randomization

- Patient was not referred to the study