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A Phase 4 Open-Label Pilot Study of the Safety and Tolerability of High Dosage of CIFN Plus RBV Administered Daily for 48 Weeks in HCV Genotype 1 Infected Patients Who Are Nonresponders to Prior Pegylated Interferon Alfa Plus RBV Therapy.

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Trial Profile

A Phase 4 Open-Label Pilot Study of the Safety and Tolerability of High Dosage of CIFN Plus RBV Administered Daily for 48 Weeks in HCV Genotype 1 Infected Patients Who Are Nonresponders to Prior Pegylated Interferon Alfa Plus RBV Therapy.

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 23 Oct 2018

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At a glance

  • Drugs Interferon alfacon-1 (Primary) ; Ribavirin (Primary)
  • Indications Hepatitis C
  • Focus Adverse reactions

    • Most Recent Events

    • 16 Apr 2008 Status changed from in progress to completed according to ClinicalTrials.gov.
    • 14 Sep 2006 New trial record.

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