This is a Phase 2, randomized, double-blind, placebo-controlled, parallel-group study to evaluate the efficacy, safety, and tolerability of TNX-601 ER monotherapy versus placebo in patients with Major Depressive Disorder (MDD).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
132
Patients will take 1 tablet orally once daily for 6 weeks.
Patients will take 1 tablet orally once daily for 6 weeks.
Montgomery Asberg Depression Rating Scale (MADRS)
Change from Baseline (Visit 2) in the MADRS total score at Week 6. Scores range from 0 to 60. Lower scores indicate less depression.
Time frame: Day 1 and Week 6
Clinical Global Impression of Severity (CGI-S)
Change from Baseline (Visit 2) in the Clinical Global Impression of Severity Scale (CGI-S) score at Week 6. Scores range from 1 to 7. Lower scores indicate less severe illness.
Time frame: Day 1 and Week 6
Sheehan Disability Scale (SDS)
Change from Baseline (Visit 2) in the Sheehan Disability Scale (SDS) total score at Week 6. Scores range from 0 to 30. Lower scores indicate less impairment to activities.
Time frame: Day 1 and Week 6
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...and 17 more locations