CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 2,430 enrolled
Drug / intervention
PegIFN-2b +1 morebiological
Likely dose
Not stated in 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/NCT00724893
NCT00724893N/ACompleted

Pegetron® Redipen™ Prospective Optimal Weight-based Dosing Response Program

Merck Sharp & Dohme LLC·observational·Posted Jul 30, 2008·Updated Aug 14, 2015

In Brief

An observational study evaluating PegIFN-2b and Ribavirin for Hepatitis C, Chronic and Hepatitis C. Completed, enrolled 2,430 participants.

Detailed Summary

Treatment compliance is a key success factor in obtaining the full benefit of Pegetron (peginterferon alfa-2b \[PegIFN-2b\] plus ribavirin combination) therapy for patients. Treatment-naïve patients with chronic hepatitis C (CHC) in Canada to whom Pegetron Redipen was prescribed will receive Pegetron Redipen therapy in accordance with approved labeling. The study will assess the effect of the newly approved Pegetron Redipen on treatment compliance and its effect on sustained virologic response rates. Sustained virologic response is defined as negative hepatitis C virus ribonucleic acid (HCV-RNA) six months post-treatment.

Study Details

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

Timeline

N/ACompletedFinished
20052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedJul 30, 2008
Enrollment StartAug 1, 2005
Primary CompletionAug 1, 2012
TodayJul 2, 2026
Enrollment to primary: 7 yearsPosted 17.9 years ago

Interventions

PegIFN-2bbiological

PegIFN-2b powder for solution adminstered subcutaneously using the newly approved Redipen. Dosing per approved labeling

Ribavirindrug

Ribavirin capsules administered orally. Dosing in accordance with approved labelling.