A Phase I, Open-Label, Single Centre Study Designed to Determine the Absolute Bioavailability of ABT-450 (150 mg) and ABT-267 (25 mg) When Administered as an Oral Co-Formulated Product With Ritonavir (100 mg), ABT 450/r/ABT 267, to Healthy Adult Subjects

Trial Profile

A Phase I, Open-Label, Single Centre Study Designed to Determine the Absolute Bioavailability of ABT-450 (150 mg) and ABT-267 (25 mg) When Administered as an Oral Co-Formulated Product With Ritonavir (100 mg), ABT 450/r/ABT 267, to Healthy Adult Subjects

Completed
Phase of Trial: Phase I

Latest Information Update: 19 Apr 2014

At a glance

  • Drugs Ombitasvir/paritaprevir/ritonavir (Primary)
  • Indications Hepatitis C
  • Focus Pharmacokinetics
  • Sponsors AbbVie
  • Most Recent Events

    • 17 Feb 2014 Status changed from recruiting to completed as reported by ClinicalTrials.gov record.
    • 12 Feb 2014 New trial record
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