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
  • Depression
  • Study Drug
  • Rapastinel
  • Placebo
  • 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
    Showing {first} - {last} of {total} Results