The study will evaluate the efficacy, safety, and tolerability of 450 milligrams (mg) or 225 mg of Rapastinel compared to placebo in the prevention of relapse in participants with major depressive disorder (MDD).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
363
Rapastinel 450 mg or 225 mg (prefilled syringe, weekly intravenous IV administration) or Rapastinel 450 mg or 225 mg (prefilled syringe, clinically driven schedule IV administration, variable interval, placebo on intervening weeks)
Placebo (prefilled syringe, weekly IV administration)
Time to First Relapse During the 52 Weeks of the Double-Blind Treatment Period (DBTP)
The time in days to first relapse is defined as the number of days from the date of randomization to the first relapse.
Time frame: 52 Weeks
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