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Interventional, randomized, double-blind, placebo-controlled study of the efficacy and safety of initial administration of 25 mg vortioxetine intravenously with 10 mg/day vortioxetine orally in patients with Major Depressive Disorder

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Trial Profile

Interventional, randomized, double-blind, placebo-controlled study of the efficacy and safety of initial administration of 25 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: 19 Aug 2020

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At a glance

Most Recent Events

  • 07 Aug 2020 Primary endpoint (Change from baseline (Day 0) to Day 1 (24 h post-infusion) in MADRS-6 subscale score) has not been met, as per Results published in the International Clinical Psychopharmacology
  • 07 Aug 2020 Results published in the International Clinical Psychopharmacology
  • 28 Aug 2019 Status changed from recruiting to completed.

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