CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 150 enrolled
Drug / intervention
Peginterferon alfa-2b +1 morebiological
Likely dose
Peginterferon alfa-2b 50 μgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00759109
NCT00759109Phase 3Completed

Long-term Pegylated Alfa-2b Interferon Therapy of Patients With Hepatitis C-related Cirrhosis and High Liver Cell Proliferation: a Multicenter Study of Hepatocellular Carcinoma Prevention in Patients Non-responders to Combined Therapy With Alpha Interferon + Ribavirin or Peginterferon Alpha + Ribavirin or to Interferon Monotherapy

Merck Sharp & Dohme LLC·interventional·Posted Sep 25, 2008·Updated Apr 7, 2017

In Brief

A Phase 3 clinical trial evaluating Peginterferon alfa-2b and Observation (no treatment) for Carcinoma, Hepatocellular. Completed, enrolled 150 participants.

Detailed Summary

This study aims to compare the role of peginterferon α-2b (50 μg/week) vs. control (no treatment) in the prevention of hepatocellular carcinoma, in adult patients with cirrhosis and initial signs of portal hypertension who did not respond to previous combined therapy with interferon alfa + ribavirin or peginterferon alfa + ribavirin or to interferon alfa monotherapy and with a high proliferation rate before entering the study. The duration of treatment will be 3 years, and the follow-up period will be 2 years.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
Countries--
Collaborators--

Timeline

Phase 3CompletedFinished
20022003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedSep 25, 2008
Enrollment StartMar 1, 2002
Primary CompletionNov 1, 2009
TodayJul 2, 2026
Enrollment to primary: 7.7 yearsPosted 17.8 years ago

Interventions

Peginterferon alfa-2bbiological

Peginterferon alfa-2b, 50 μg, weekly, SC, for a period of 3 years.

Observation (no treatment)other

No treatment was given to participants enrolled in the control arm (Arm B).