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Taking people in RomaniaPhase 3

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
Bucharest, Craiova, and Oradea, RomaniaSee the 4 sites
Phase
Phase 3

Where in Romania

  • Centru De Evaluare Si Tratament A Toxicodependentelor Pentru Tineri Sf. StelianBucharest, RomaniaTaking people
  • Spitalul Clinic de Psihiatrie Prof Dr Alexandru ObregiaBucharest, RomaniaTaking people
  • Institutul Privat de Cercetari Melchisedec, pentru Boli Autoimune, Ereditare si Rare - IPCMCraiova, RomaniaTaking people
  • Spitalul Clinic Judetean De Urgenta BihorOradea, RomaniaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

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.

ClinicalTrials.gov NCT06966401 · EU CTIS 2024-519423-24-00