Multicenter, open-label, long-term extended access treatment protocol in adult patients with a primary diagnosis of MDD.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
230
Rapastinel 450 mg (prefilled syringe, weekly or biweekly or up to 4 weeks at the investigator's discretion intravenous IV administration)
Count of Participants Experiencing One or More Treatment Emergent Adverse Events (TEAEs)
A Treatment Emergent Adverse Event was considered any unfavorable and unintended sign, symptom, or disease associated with the use of the study drug, whether or not considered related to the study drug. An Adverse Drug Reaction was a harmful and unintended reaction that is incurred during routine administration or use of the drug, whose causal relationship with the drug cannot be excluded.
Time frame: Up to 45 Weeks
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University of Alabama at Birmingham
Birmingham, Alabama, United States
Harmonex Neuroscience Research
Dothan, Alabama, United States
NoesisPharma
Phoenix, Arizona, United States
Woodland International Research Group
Little Rock, Arkansas, United States
Woodland Research Northwest
Rogers, Arkansas, United States
California Pharmaceutical Research Institute, Inc
Anaheim, California, United States
Southern California Research LLC.
Beverly Hills, California, United States
ATP Clinical Research Inc.
Costa Mesa, California, United States
ProScience Research Group
Culver City, California, United States
Pharmacology Research Institute
Encino, California, United States
...and 64 more locations