Condition: Major Depressive Disorder · Sponsor: Neurocrine Biosciences
The primary objective of this study is to evaluate the efficacy of NBI-1065845 compared with placebo as an adjunctive treatment in delaying relapse of depressive symptoms (maintenance of effect) in participants with MDD.
This description comes directly from the study's public registry record.
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| Neurocrine Clinical Site | Oceanside, California, United States | Recruiting |
| Neurocrine Clinical Site | Orange, California, United States | Recruiting |
| Neurocrine Clinical Site | San Jose, California, United States | Recruiting |
| Neurocrine Clinical Site | New Haven, Connecticut, United States | Recruiting |
| Neurocrine Clinical Site | Miami Gardens, Florida, United States | Recruiting |
| Neurocrine Clinical Site | Orlando, Florida, United States | Recruiting |
| Neurocrine Clinical Site | Palm Bay, Florida, United States | Recruiting |
| Neurocrine Clinical Site | Tampa, Florida, United States | Recruiting |
| Neurocrine Clinical Site | Iowa City, Iowa, United States | Recruiting |
| Neurocrine Clinical Site | Marrero, Louisiana, United States | Recruiting |
| Neurocrine Clinical Site | O'Fallon, Missouri, United States | Recruiting |
| Neurocrine Clinical Site | Albuquerque, New Mexico, United States | Recruiting |
+ 48 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT07196501