Efficacy and safety of tianeptine oral administration (25 to 50 mg/day) in elderly patients suffering from Major Depressive Disorder. A 8-week, randomized, double-blind, flexible-dose, parallel groups, placebo-controlled, international, multicentre study with escitalopram as active control, followed by an optional double-blind extension treatment period of 16 weeks.

Trial Profile

Efficacy and safety of tianeptine oral administration (25 to 50 mg/day) in elderly patients suffering from Major Depressive Disorder. A 8-week, randomized, double-blind, flexible-dose, parallel groups, placebo-controlled, international, multicentre study with escitalopram as active control, followed by an optional double-blind extension treatment period of 16 weeks.

Completed
Phase of Trial: Phase III

Latest Information Update: 03 Mar 2016

At a glance

  • Drugs Tianeptine (Primary) ; Escitalopram
  • Indications Major depressive disorder
  • Focus Registrational; Therapeutic Use
  • Sponsors IRIS
  • Most Recent Events

    • 02 Mar 2016 Status changed from recruiting to completed, according to European Clinical Trials Database record.
    • 09 Sep 2013 New trial record
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