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
For general inquiries, please contact
Results Available
Statistical Analysis Plan
Available Language(s): English
Protocol
Available Language(s): English
Study Details
Medical Condition
Study Drug
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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