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Interventional, randomised, double-blind, parallel-group study of the efficacy and safety of initial administration of 17 mg vortioxetine intravenously with 10 mg/day vortioxetine orally in patients with Major Depressive Disorder

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Trial Profile

Interventional, randomised, double-blind, parallel-group study of the efficacy and safety of initial administration of 17 mg vortioxetine intravenously with 10 mg/day vortioxetine orally in patients with Major Depressive Disorder

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 23 May 2019

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At a glance

  • Drugs Vortioxetine (Primary) ; Vortioxetine (Primary)
  • Indications Major depressive disorder
  • Focus Therapeutic Use
  • Sponsors Lundbeck A/S

    • Most Recent Events

    • 14 May 2019 Primary endpoint (Change from baseline to Week 1 in MADRS total score) has not been met as per results published in the International Clinical Psychopharmacology
    • 14 May 2019 Results published in the International Clinical Psychopharmacology
    • 05 Jul 2017 Status changed from active, no longer recruiting to completed.

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