The purpose is to study the efficacy and safety of ABT-436 in Major Depressive Disorder.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
19
Subjects receiving ABT-436
Subjects receiving escitalopram
Subject receiving placebo
Site Reference ID/Investigator# 85593
Little Rock, Arkansas, United States
Site Reference ID/Investigator# 87228
Primary efficacy variable will be change from baseline to Week 6 visit on Montgomery-Asberg Depression Rating Scale (MADRS) total score.
Primary efficacy variable will be change from baseline to Week 6 visit on Montgomery-Asberg Depression Rating Scale (MADRS) total score.
Time frame: Week 6
Secondary efficacy variables include change from Baseline to Week 6 on clinician-rated Hamilton Depression Rating Scale.
Secondary efficacy variables include change from Baseline to Week 6 on clinician-rated Hamilton Depression Rating Scale.
Time frame: Week 6
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Garden Grove, California, United States
Site Reference ID/Investigator# 87214
National City, California, United States
Site Reference ID/Investigator# 87220
Oakland, California, United States
Site Reference ID/Investigator# 87215
Bradenton, Florida, United States
Site Reference ID/Investigator# 87225
South Miami, Florida, United States
Site Reference ID/Investigator# 85594
Atlanta, Georgia, United States
Site Reference ID/Investigator# 85580
Marlton, New Jersey, United States
Site Reference ID/Investigator# 87227
Brooklyn, New York, United States
Site Reference ID/Investigator# 87223
New York, New York, United States
...and 8 more locations