* Study population:Person with HBeAg negative CHB on TDF/ETV for more than 1 year * Study design:Prospective,Interventional (single arm study) * Sample size: All the patients fulfilling the inclusion criteria will be included in first 6 months and subsequently followed up for 2 years * Intervention: Peg IFN 2b 1.5mcg/kg once every week for 48 weeks * Monitoring and assessment: LFT,HBV DNA and HbsAg at baseline, 4 weeks, 12 weeks,24 weeks,48 weeks ,72 weeks and 96 weeks, CBC every month and Thyroid function Test every 3rd month * Adverse effects: The most frequently reported side effects of IFN-based therapy are flu-like symptoms, headache, fatigue, myalgia, alopecia, and local reaction at the injection site. Peg-IFN have myelosuppressive effects; however, neutropenia\\1000/mm3 and thrombocytopenia \\500,000/ mm3 are not common unless patients already have cirrhosis
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
118
Peg IFN 2b 1.5mcg/kg once every week for 48 weeks
Institute of Liver and Biliary Sciences
New Delhi, National Capital Territory of Delhi, India
Sustained Virological Response-HBV DNA<2000IU/ml after stopping PEG IFN alpha
Time frame: 6 months
Loss of HBsAg after 48 weeks of PEG IFN alpha
Time frame: 48 weeks
End treatment Response: HBV-DNA -undetectable after 48 weeks of PEG-IFN
Time frame: 48 weeks
Sustained Off treatment Virological response defined as No clinical relapse during 1 year follow up after stopping therapy
Time frame: 1 year
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