WHO ICTRP trial

Vortioxetine to Prevent Return of Symptoms in Children With Depression

EUCTR2010-020493-42-BG · EU Clinical Trials Register · Not Recruiting

Key facts

Trial ID EUCTR2010-020493-42-BG
Public title Vortioxetine to Prevent Return of Symptoms in Children With Depression
Scientific title A Double-blind, Randomized, Placebo-controlled, Multicentre, Relapse-prevention Study of Vortioxetine in Paediatric Patients Aged 7 to 11 Years With Major Depressive Disorder
Primary sponsor H. Lundbeck A/S
Registry EU Clinical Trials Register
Recruitment status Not Recruiting
Study type Interventional clinical trial of medicinal product
Phase Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): no Therapeutic confirmatory - (Phase III): yes Therapeutic use (Phase IV): no
Countries United States;Serbia;Mexico;Argentina;Spain;Poland;Ukraine;Russian Federation;Bulgaria;Latvia;Colombia
Conditions Major Depressive Disoder;Therapeutic area: Psychiatry and Psychology [F] - Mental Disorders [F03]
Interventions Trade Name: Brintellix 20 mg encapsulated film-coated tablets Product Name: Vortioxetine Pharmaceutical Form: Film-coated tablet INN or Proposed INN: VORTIOXETINE CAS Number: 508233-74-7 Concentration unit: mg milligram(s) Concentration…
Registration date Mar 25, 2021
Target size 150
Secondary IDs 13546A
Registry page clinicaltrialsregister.eu

At a glance

  • No Results available

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About WHO ICTRP trial registrations

The WHO ICTRP combines trial registrations from primary registries worldwide into a single searchable index. Contact and ethics-committee details are not shown here.

Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

Browse all WHO ICTRP trial registrations