A Study of Rapastinel for Rapid Treatment of Depression and Suicidality in Major Depressive Disorder
Study Identifier
RAP-MD-20
CT.gov Identifier
EudraCT Identifier
Not available
EUCTIS ID
Not available
For general inquiries, please contact
Results Available
Statistical Analysis Plan
Available Language(s): English
Protocol
Available Language(s): English
Study Details
Medical Condition
Study Drug
Phase
Phase 2
Sex
Female & Male
Age
18 - 65 Years
Protocol Summary
The study will evaluate the efficacy, safety, and tolerability of 450 milligrams (mg) of Rapastinel, compared to placebo in adult patients with major depressive disorder (MDD) who are at imminent risk of suicide.
Study Locations
Location
Status
Location
The Board of Trustees of the University of Alabama for the University of Alabama at Birmingham
Birmingham, Alabama, United States, 35294-0107
Status
Not applicable
Location
Collaborative NeuroScience Network, LLC
Garden Grove, California, United States, 92845
Status
Not applicable
Location
Behavioral Research Specialists, LLC
Glendale, California, United States, 91206-4282
Status
Not applicable
Location
Asclepes Research Centers
Panorama City, California, United States, 91402
Status
Not applicable
Location
Institute of Living
Hartford, Connecticut, United States, 06106
Status
Not applicable
Location
Innovative Clinical Research, Inc
Hialeah, Florida, United States, 33012
Status
Not applicable
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