Study of the Efficacy & Safety of Initial Administration of 17 mg

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NCT number	NCT02919501
Study type	Interventional
Source	H. Lundbeck A/S
Contact
Status	Completed
Phase	Phase 2
Start date	September 27, 2016
Completion date	April 27, 2017

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

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms