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
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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
  • 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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