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Prognostic Factors of Long-term Response to Treatment With Pegylated Interferon Alfa-2a in Patients With HbeAg-negative Chronic Hepatitis B. (Perseas)
This observational, multi-center, open-label study will evaluate the prognostic factors of long-term-response and the safety of Pegasys (peginterferon alfa-2a) in patients with HbeAg-negative chronic hepatitis B. Data will be collected for 96 weeks.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Alexandroupoli, Greece
Athens, Greece
Athens, Greece
Athens, Greece
Athens, Greece
Athens, Greece
Athens, Greece
Larissa, Greece
Pátrai, Greece
Piraeus, Greece
Start Date
May 1, 2009
Primary Completion Date
November 1, 2012
Completion Date
November 1, 2012
Last Updated
November 2, 2016
107
ACTUAL participants
Lead Sponsor
Hoffmann-La Roche
NCT04166266
NCT06550622
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT05922306