Trial Profile

Interventional, Randomised, Double-blind 4-way Crossover Study Comparing the Gastro-intestinal Tolerability and Absorption Profile of Vortioxetine After Administration of Modified-release Formulations and Immediate-release Formulation in Healthy Women

Status: Completed

Phase of Trial: Phase I

Latest Information Update: 11 Dec 2014

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At a glance

Drugs Vortioxetine (Primary)
Indications Anxiety disorders; Generalised anxiety disorder; Major depressive disorder
Focus Adverse reactions; Pharmacokinetics
Sponsors Lundbeck A/S

08 Sep 2014 Status changed from recruiting to completed as reported by ClinicalTrials.gov record.
18 Apr 2014 New trial record

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