Summary:
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The purpose of this study is to evaluate the effectiveness and safety of an investigational compound for Major Depressive Disorder. The study consists of a 6 week outpatient study treatment period, followed by a safety follow up period. All procedures and study visits will take place at CBH Health located in Gaithersburg, MD.
Qualified Participants Must:
Male or Female, Ages 18-75
Diagnosis of Major Depressive Disorder and currently experiencing a Major Depressive Episode
Be in good physical health as ascertained by medical history, physical examination, and clinical laboratory evaluations
History of bipolar disorder, schizophrenia, or schizoaffective disorder is exclusionary.
No seizure disorder, strokes or tumor
Current diagnosis of substance abuse or within past 6 months is exclusionary
Current sucidal ideation or a suicide attempt within the past year is exclusionary
Qualified Participants May Receive:
Compensation will be provided.