CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 2,343 enrolled
Drug / intervention
Peginterferon alfa-2a [Pegasys] +1 moredrug
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/NCT01066793
NCT01066793N/ACompleted

Prospective Observational Study on Predictors of Early On-treatment Response and Sustained Virological Response in a Cohort of Treatment naïve HCV-infected Patients Treated With Pegylated Interferons.

Hoffmann-La Roche·observational·Posted Feb 10, 2010·Updated May 9, 2016

In Brief

An observational study evaluating Peginterferon alfa-2a [Pegasys] and Peginterferon alfa-2b [PegIntron®] for Hepatitis C, Chronic. Completed, enrolled 2,343 participants across 100 sites in 4 countries.

Detailed Summary

This observational study will assess predictors of early on-treatment and sustained virological response in treatment-naïve patients with chronic hepatitis C initiated on treatment with Pegasys (peginterferon alfa-2a) or peginterferon alfa-2b and ribavirin. Data will be collected during the treatment period (24 or 48 weeks) and 12 and 24 weeks after the end of treatment. Target sample size is \<2000.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesBelgium, Ireland, Italy, United Kingdom
Collaborators--

Timeline

N/ACompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedFeb 10, 2010
Enrollment StartOct 1, 2007
Primary CompletionMar 1, 2011
Study CompletionMay 1, 2011
TodayJul 2, 2026
Enrollment to primary: 3.4 yearsPosted 16.4 years ago

Interventions

Peginterferon alfa-2a [Pegasys]drug

Peginterferon/ribavirin treatment period as prescribed by treating physician (e.g. 24 or 48 weeks) and treatment-free follow-up period of 24 weeks.

Peginterferon alfa-2b [PegIntron®]drug

Peginterferon/ribavirin treatment period as prescribed by treating physician (e.g. 24 or 48 weeks) and treatment-free follow-up period of 24 weeks.