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
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Study Complete

Results Available

Protocol
Available Language(s): English
Statistical Analysis Plan
Available Language(s): English

Study Details

Medical Condition
  • Depression
  • Study Drug
  • Rapastinel
  • Placebo-matching Rapastinel
  • 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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