Long-term safety study of NBI-1065845 added to treatment for depression
Tests NBI-1065845 as an added treatment in adults with major depressive disorder.
Plain-language title generated from the registry record
Registry title: Long-Term Study to Assess the Safety and Tolerability of NBI-1065845 as an Adjunctive Treatment in Participants With Major Depressive Disorder (MDD)
Key facts
- Where
- Kirdzhali, Plovdiv, Ruse, Sofia, Sofiya, and Varna, BulgariaSee the 8 sites
- Phase
- Phase 3
Where in Bulgaria
- Medical Center Lifemed EOODKirdzhali, BulgariaTaking people
- Medical Center Mentalcare Ltd.Plovdiv, BulgariaTaking people
- Center For Mental Health Ruse EOODRuse, BulgariaTaking people
- Medical Center Intermedica Ltd.Sofia, BulgariaTaking people
- Diagnostic And Consultation Centre St.Vrach And St.St. Kuzma And Damian OODSofiya, BulgariaTaking people
- Medical Center Hera EOODSofiya, BulgariaTaking people
- Medical Center Saint Naum EOODSofiya, BulgariaTaking people
- Diagnostics-Consultancy Center Mladost M Varna OODVarna, BulgariaTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Neurocrine Biosciences
- Trial code
- NCT06966401EU 2024-519423-24-00
- Record updated
- 2 November 2026
- Original description
This study will evaluate the long-term safety and tolerability of NBI-1065845 as an adjunctive treatment in participants with MDD.Read full original descriptionShow less
A Long-Term, Open-Label Study to Assess the Safety and Tolerability of NBI-1065845 as Adjunctive Treatment in Subjects With Major Depressive Disorder (MDD)
This study will evaluate the long-term safety and tolerability of NBI-1065845 as an adjunctive treatment in participants with MDD.
Inclusion: Participant has a primary diagnosis of recurrent MDD (moderate or severe) or persistent depressive disorder; Participant has had an inadequate response to oral antidepressant treatments in the current episode of depression; Participant must have been taking oral antidepressants for at least 8 weeks prior to screening; Willing and able to comply with all study procedures and restrictions in the opinion of the investigator.
Exclusion: A current or prior psychiatric disorder diagnosis in the last 1 year that was the primary focus of treatment other than MDD; Are considered by the investigator to be at imminent risk of suicide or injury to self or others; Other protocol defined inclusion and exclusion criteria apply.