Compensation
$200 for each visit
Ages
18 to 70 years
Gender
Male & Female
Trial Setting
Outpatient
Duration
11 weeks
Adults with Major Depressive Disorder (MDD), with or without Anxious Distress.
This Phase 2, randomized, double-blind, placebo-controlled study is evaluating an investigational oral antidepressant as an add-on treatment for adults with major depressive disorder (MDD) who continue to experience moderate to severe symptoms despite taking standard antidepressant therapy. Major Depressive Disorder is a chronic and debilitating mental health condition characterized by persistent sadness, loss of interest, and impaired functioning. Although multiple antidepressants are FDA-approved, many patients do not respond adequately. This study seeks to determine whether this add-on medication can improve depressive symptoms compared with placebo. The trial will assess both the efficacy and safety of the study medication, with the goal of better understanding its potential as a personalized, well-tolerated treatment option for individuals with depression.
The Details
- 11 weeks
- 18 to 70 years
- Male & Female
- $200 for each visit
- Outpatient
Participants Must:
- Have a primary diagnosis of Major Depressive Disorder (MDD).
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