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A Phase 1, Open-Label, Parallel-Group Study to Evaluate the Pharmacokinetics, Safety and Tolerability of a Single Oral Dose of 5 mg Vortioxetine in Subjects With Normal Hepatic Function or Severe Hepatic Impairment

Trial Profile

A Phase 1, Open-Label, Parallel-Group Study to Evaluate the Pharmacokinetics, Safety and Tolerability of a Single Oral Dose of 5 mg Vortioxetine in Subjects With Normal Hepatic Function or Severe Hepatic Impairment

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 01 Dec 2018

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At a glance

  • Drugs Vortioxetine (Primary)
  • Indications Anxiety disorders; Generalised anxiety disorder; Major depressive disorder
  • Focus Pharmacokinetics
  • Sponsors Takeda
  • Most Recent Events

    • 01 Dec 2018 Results from this and 3 other trials published in the Clinical Pharmacology in Drug Development.
    • 03 Jun 2015 Status changed from recruiting to completed as per ClinicalTrials.gov record.
    • 25 Jul 2014 Status changed from not yet recruiting to recruiting as reported by ClinicalTrials.gov.
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