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NCT03766867

Vortioxetine Intravenous Infusion at Initiation of Oral Treatment With Vortioxetine in Patients With Depression

Completed Phase 2 Last updated 29 August 2019
What this trial tests

Phase 2 trial testing Vortioxetine infusion 25 mg in Major Depressive Disorder in 80 participants. Completed in 28 August 2019.

Timeline
3 December 2018
Primary endpoint
31 July 2019
28 August 2019

Quick facts

Lead sponsorH. Lundbeck A/S
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment80
Start date3 December 2018
Primary completion31 July 2019
Estimated completion28 August 2019
Sites13 locations across Estonia, Bulgaria, Latvia

Drugs / interventions tested

Conditions studied

Sponsor

H. Lundbeck A/S — full company profile →

Who can join

Adults 18 to 65, any sex, with Major Depressive Disorder. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to evaluate the efficacy and safety of vortioxetine given as a single intravenous dose of 25 mg at initiation of an oral vortioxetine regimen of 10 mg/day for 7 days

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Intravenous vortioxetine to accelerate onset of effect in major depressive disorder: a 7-day randomized, double-blind, placebo-controlled exploratory study.
    Rancans E, Zambori J, Dalsgaard M, Baayen C, et al · · 2020 · cited 8× · PMID 32784346 · DOI 10.1097/yic.0000000000000326

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Other recruiting trials for Major Depressive Disorder

Currently open trials in the same condition.

Other H. Lundbeck A/S trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03766867.

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