A Study of Rapastinel as Adjunctive Therapy in Major Depressive Disorder (RAP-MD-01)
Study Identifier
RAP-MD-01
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 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
Southern California Research LLC.
Beverly Hills, California, United States, 90036
Status
Not applicable
Location
ATP Clinical Research Inc.
Costa Mesa, California, United States, 92626
Status
Not applicable
Location
Pharmacology Research Institute
Encino, California, United States, 91316
Status
Not applicable
Location
Collaborative Neuroscience Network, LLC
Garden Grove, California, United States, 92845
Status
Not applicable
Location
Synergy San Diego
Lemon Grove, California, United States, 91945
Status
Not applicable
Location
Pharmacology Research Institute
Los Alamitos, California, United States, 90720
Status
Not applicable
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