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Taking people in Olaszország3. fázis

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
Milan, Rome és Turin, OlaszországSee the 3 sites
Phase
3. fázis

Where in Olaszország

  • Ospedale San Raffaele S.r.l.Milan, OlaszországTaking people
  • Fondazione Policlinico Universitario Agostino Gemelli IRCCSRome, OlaszországTaking people
  • Azienda Ospedaliera Universitaria Citta Della Salute E Della Scienza Di TorinoTurin, OlaszországTaking 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
2026. november 2.
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