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Prospective, Observational Study of Predictors of the Effectiveness of Pegylated Interferon in a Cohort of Patients With Hepatitis C in Georgia
This prospective observational study will investigate predictive values of virological response in pegylated interferon alfa-2a (Pegasys)/ribavirin (Copegus) treatment-naive participants with chronic hepatitis C. Participants will be treated with pegylated interferon alfa-2a and ribavirin as prescribed by the physician. Data will be collected for a maximum of 96 weeks.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Hepatology Clinic Hepa
Tbilisi, Georgia
Infectious Diseases, AIDS and Clinical Immunology Research Center
Tbilisi, Georgia
Ltd Mrcheveli
Tbilisi, Georgia
Start Date
April 6, 2011
Primary Completion Date
October 20, 2015
Completion Date
October 20, 2015
Last Updated
October 3, 2017
516
ACTUAL participants
Pegylated Interferon Alfa-2a
DRUG
Ribavirin
DRUG
Lead Sponsor
Hoffmann-La Roche
NCT05870969
NCT03987503
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 ConditionsNCT04382404