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.
Status:
Completed
Phase of Trial:
Phase III
Latest Information Update: 23 Jul 2018
Price :
$35
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At a glance
- Drugs Tianeptine (Primary) ; Escitalopram
- Indications Major depressive disorder
- Focus Registrational; Therapeutic Use
- Sponsors IRIS; Servier
- 03 Jul 2018 Primary endpoint has been met. (HAM-D 17 total score), as reported in an article published in the Journal of Clinical Psychiatry.
- 03 Jul 2018 Results published in the Journal of Clinical Psychiatry
- 02 Mar 2016 Status changed from recruiting to completed, according to European Clinical Trials Database record.