Ypeginterferon alfa-2b
Drugsc, qw, 48 weeks.
NCT Number: NCT01760122
This study is aimed to assess the efficacy and safety of Peginterferon alfa-2b (40kD, Y-shape), in a dose of 180μg/week, in chronic hepatitis B patients, and collects sufficient evidences for the listed of the studied drug.
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Notify Me18 year–65 year
All sexes
Interventional
Phase 3
Xiamen Hospital of T.C.M, Xiamen, Fujian, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
sc, qw, 48 weeks.
sc, qw, 48 weeks.
Time frame: 24 weeks after the cessation of treatment
Time frame: week 12, 24, 48 from treatment starting
Time frame: week 4, 12, 24, 48 and 72 from treatment starting
Time frame: week 12, 24, 48 and 72 from treatment starting
Time frame: week 12, 24, 48 and 72 from treatment starting
Time frame: week 12, 24, 48 and 72 from treatment starting
Xiamen Amoytop Biotech Co., Ltd.
Industry
A Phase 3, Randomized, Multi-center, Active-controlled, Open-label Study to Evaluate the Efficacy and Safety of Peginterferon Alfa-2b (40kD, Y Shape) in Chinese Chronic Hepatitis B Patients.
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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