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A Long-Term, Open-Label, Flexible-Dose, Extension Study Evaluating the Safety and Tolerability of Lu AA21004 in Subjects With Major Depressive Disorder.

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Trial Profile

A Long-Term, Open-Label, Flexible-Dose, Extension Study Evaluating the Safety and Tolerability of Lu AA21004 in Subjects With Major Depressive Disorder.

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 06 Oct 2021

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At a glance

  • Drugs Vortioxetine (Primary)
  • Indications Major depressive disorder
  • Focus Adverse reactions; Registrational
  • Sponsors Takeda; Takeda Global Research and Development Center

    • Most Recent Events

    • 01 Sep 2015 Pooled analysis results (NCT00761306, NCT00694304, NCT00707980, NCT01323478 and NCT01152996) presented at the 28th Annual Congress of the European College of Neuropsychopharmacology.
    • 01 Sep 2015 Pooled subgroup analysis results ((NCT00761306, NCT00694304, NCT00707980, NCT01323478 and NCT01152996)) presented at the 28th Annual Congress of the European College of Neuropsychopharmacology.
    • 08 Sep 2010 Status changed from active, no longer recruiting to completed as reported by ClinicalTrials.gov.

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