Study of Rapastinel as Monotherapy in Patients With Major Depressive Disorder (MDD)

Study Identifier
RAP-MD-30
CT.gov Identifier
EudraCT Identifier
EUCTIS ID
Not available
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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 3
    Sex
    Female & Male
    Age
    18 - 75 Years

    Protocol Summary

    The study will evaluate the efficacy, safety, and tolerability of 225 milligrams (mg) and 450 milligrams (mg) of Rapastinel, compared to placebo in participants with major depressive disorder (MDD).

    Study Locations

    Location
    Status
    Location
    Bugát Pál Hospital, Clinexpert
    Gyöngyös, Hungary, 3200
    Status
    Not applicable
    Location
    Himorogi Psychiatric Institute
    Ichigayatamachi, Japan, 162-0843
    Status
    Not applicable
    Location
    Kishiro Mental Clinic
    Kawasaki-shi, Japan, 214-0014
    Status
    Not applicable
    Location
    Tatsuta Clinic
    Kobe, Japan, 651-0097
    Status
    Not applicable
    Location
    Medical corporation Sato-Kai Yuge Hospital
    Kumamoto, Japan, 861-8002
    Status
    Not applicable
    Location
    Sagaarashiyama-Tanaka Clinic
    Kyoto, Japan, 616-8421
    Status
    Not applicable
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