Long-term Safety Study of Rapastinel as Adjunctive Therapy in Patients With Major Depressive Disorder

Study Identifier
RAP-MD-06
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
  • Depression
  • Study Drug
  • Rapastinel
  • Phase
    Phase 3
    Sex
    Female & Male
    Age
    18 - 65 Years

    Protocol Summary

    This study will evaluate the long-term safety and tolerability of rapastinel as an adjunctive to antidepressant therapy (ADT) in patients 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, Inc.
    Dothan, Alabama, United States, 36303
    Status
    Not applicable
    Location
    NoesisPharma
    Phoenix, Arizona, United States, 85032
    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
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