An open-label, single-dose, parallel group study to evaluate the effects of age and gender on the pharmacokinetics, safety, and tolerability of HCV-796 administered orally to healthy subjects

Trial Profile

An open-label, single-dose, parallel group study to evaluate the effects of age and gender on the pharmacokinetics, safety, and tolerability of HCV-796 administered orally to healthy subjects

Completed
Phase of Trial: Phase I

Latest Information Update: 16 Apr 2008

At a glance

  • Drugs Nesbuvir (Primary)
  • Indications Hepatitis C
  • Focus Pharmacokinetics
  • Sponsors Wyeth
  • Most Recent Events

    • 16 Apr 2008 Development of nesbuvir has been discontinued due to safety issues, according to a ViroPharma media release.
    • 11 Apr 2008 Status changed from recruiting to completed.
    • 12 Dec 2006 New trial record.
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