The purpose of this study is to evaluate the safety and tolerability of brexpiprazole as adjunctive treatment in an elderly population with major depressive disorder and an inadequate response to antidepressant treatment
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
132
Weeks 1-4 titration from 0.5 up to 2 mg once daily, in weekly steps. For the rest of the 26 treatment weeks, maintenance with 1-3 mg once daily. Tablets for oral use once daily during 26 weeks. Tablet strengths: 0.5 mg, 1 mg, 2 mg and 3 mg.
Citalopram, ecitalopram, fluoxetine, sertraline, paroxetine IR, paroxetine CR, venlafaxine IR, venlafaxine XR (extended release), desvenlafaxine, duloxetine, mirtazapine, agomelatine, bupropion; dosing according to label
US012
Arcadia, California, United States
Number of Patients With Treatment-Emergent Adverse Events
Treatment-emergent adverse event is an adverse event that started or increased in intensity at or after baseline visit
Time frame: Baseline to 30 weeks
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US004
Miami, Florida, United States
US007
Orlando, Florida, United States
US006
Smyrna, Georgia, United States
US002
O'Fallon, Missouri, United States
US010
Toms River, New Jersey, United States
US005
New York, New York, United States
US008
New York, New York, United States
US003
Staten Island, New York, United States
US014
Oklahoma City, Oklahoma, United States
...and 24 more locations