Louisville,
Kentucky
40202
Purpose:
The purpose of this study is to compare the effects on depressive symptoms of subjects who
discontinue serotonergic antidepressants (a certain type of antidepressant, such as Prozac,
that works on serotonin receptors in the brain) with the effects on depressive symptoms of
subjects who continue to take serotonergic antidepressants. During this study, subjects will
also be presented with the opportunity to undergo genetic testing for the serotonin gene
transporter which has a short or long form. This is being done because it has been
demonstrated that genetic testing improves outcome while treating treatment-resistant
depression.
Criteria:
Inclusion Criteria:
- Subjects must be a man or woman 18 to 70 years of age, inclusive.
- Subject must meet criteria for a major depressive disorder as confirmed by the Mini
International Neuropsychiatric Interview [MINI].
- Subjects must have a current Treatment-Resistant Depression as defined below.
- Subjects must have been taking serotonergic antidepressants (serotonin reuptake
inhibitor or monoamine oxidase inhibitor) for at least 2 years but not more than 4
years, and have failed 2 previous medication trial for the current episode. Current
Montgomery-Åsberg Depression Rating Scale [MADRS] score must be equal to or more than
25.
- Subject must be medically stable.
- Female subjects must have a negative urine pregnancy test at screening, and agree to
avoid pregnancy during the study.
- Each subject must sign an informed consent form indicating that he/she understands the
purpose of the study and the procedures required and are willing to participate in the
study.
- Subject must be able to participate in symptom measurement.
Exclusion Criteria:
- Subject has a current Diagnostic and Statistical Manual of Mental Disorders-5 [DSM-5]
diagnosis of bipolar disorder or has a positive screening for bipolar disorder by Mini
International Neuropsychiatric Interview [MINI] or Mood Disorder Questionnaire [MDQ].
- Subject has a current DSM-5 diagnosis of schizophrenia, schizoaffective disorder,
autistic disorder, or intellectual disability.
- Subject has a substance use disorder (except for nicotine or cannabis) within 3 months
prior to screening or has a positive drug screen test for any recreational drugs at
the time of screening with the exception of Cannabis.
- Subject has evidence of any clinically significant, unstable medical problems that may
create a safety risk for a subject, interfere with study participation, or make
results difficult to interpret.
- Subject is at imminent risk of suicide according to the investigator's clinical
judgment and/or a Columbia-Suicide Severity Rating Scale (C-SSRS) 3 or more at any
time in the study.
- Subject is a woman who is pregnant, breast-feeding or planning to become pregnant
while enrolled in the study.
- Subject has any condition (according to the investigator) for which participation will
not be the best interest for the subject or it can prevent, limit or confound the
protocol-specified assessments.