A Study of Rapastinel as Adjunctive Therapy in the Prevention of Relapse in Patients With Major Depressive Disorder
Study Identifier
RAP-MD-04
CT.gov Identifier
EudraCT Identifier
Not available
EUCTIS ID
Not available
For general inquiries, please contact
Study Complete
Results Available
Protocol
Available Language(s): English
Statistical Analysis Plan
Available Language(s): English
Study Details
Medical Condition
Study Drug
Phase
Phase 3
Sex
Female & Male
Age
18 - 65 Years
Protocol Summary
This study will evaluate the efficacy, safety and tolerability of rapastinel 450 milligrams (mg) intravenous (IV) once weekly or once every 2 weeks versus placebo as an adjunctive treatment to ongoing anti-depressive therapy (ADT) in the prevention of relapse in participants with Major Depressive Disorder (MDD).
Study Locations
Location
Status
Location
University of Alabama at Birmingham
Birmingham, Alabama, United States, 35294
Status
Not applicable
Location
Harmonex Neuroscience Research
Dothan, Alabama, United States, 36303
Status
Not applicable
Location
NoesisPharma
Phoenix, Arizona, United States, 85032
Status
Not applicable
Location
University of Arizona Department of Psychiatry
Tucson, Arizona, United States, 85724
Status
Not applicable
Location
Woodland International Research Group
Little Rock, Arkansas, United States, 72211
Status
Not applicable
Location
Woodland Research Northwest
Rogers, Arkansas, United States, 72758
Status
Not applicable
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