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Clinical Trial Summary

To evaluate the efficacy and safety of AXS-05 relative to bupropion in subjects with treatment resistant major depressive disorder (MDD). This is a randomized, double-blind, active-controlled, 12-week, two-period study consisting of an open-label, bupropion lead-in period, and a double-blind treatment period. The trial is being conducted in subjects with treatment resistant MDD. Subjects will be considered to have treatment resistant MDD if they have had a historical inadequate response to 1 or 2 antidepressant treatments and a prospective inadequate response to treatment with bupropion during the open-label, lead-in period.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02741791
Study type Interventional
Source Axsome Therapeutics, Inc.
Contact
Status Completed
Phase Phase 3
Start date March 2016
Completion date March 20, 2020

See also
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