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A Multicenter, Randomized, Double-Blind, Active Controlled, Comparative, Fixed-Dose, Dose Response Study of the Efficacy and Safety of BMS-820836 in Patients With Treatment Resistant Major Depression (TRD).

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A Multicenter, Randomized, Double-Blind, Active Controlled, Comparative, Fixed-Dose, Dose Response Study of the Efficacy and Safety of BMS-820836 in Patients With Treatment Resistant Major Depression (TRD).

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 07 Oct 2021

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At a glance

  • Drugs Liafensine (Primary) ; Duloxetine; Escitalopram
  • Indications Major depressive disorder
  • Focus Pharmacogenomic; Therapeutic Use
  • Acronyms BMS-TRUI

    • Most Recent Events

    • 01 May 2013 Status changed from recruiting to completed as reported by ClinicalTrials.gov.
    • 07 Feb 2013 Planned End Date changed from 1 Jul 2013 to 1 May 2013 as reported by ClinicalTrials.gov.
    • 21 Aug 2012 New source identified and integrated (Clinical Trials Registry - India, CTRI2012-04-002617).

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