A Study of Rapastinel as Adjunctive Therapy in Major Depressive Disorder (RAP-MD-02)
Study Identifier
RAP-MD-02
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 two doses of rapastinel, 225 milligrams (mg) and 450 mg, compared to placebo adjunctive to antidepressant therapy (ADT) in patients with major depressive disorder (MDD) who have a partial response to ADT.
Study Locations
Location
Status
Location
University of Alabama at Birmingham
Birmingham, Alabama, United States, 35294
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
Location
California Pharmaceutical Research Institute, Inc
Anaheim, California, United States, 92804
Status
Not applicable
Location
ProScience Research Group
Culver City, California, United States, 90230
Status
Not applicable
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