An interventional study of Peginterferon alfa-2b combined and ETV in Chronic HBV Infection, sponsored by Fang Wang. Recruiting at 1 site in China. Open to participants aged 3 Years to 18 Years. Per ClinicalTrials.gov, last updated 2023-03-31.
Sponsored by Fang Wang · Not applicable, Interventional, and Treatment
There are nearly 2 million HBsAg-positive children who are in urgent need of professional diagnosis and treatment in China. Chronic hepatitis B (CHB) is the leading cause of childhood liver disease. After infected with HBV virus, some children will develop disease progression, and some even develop cirrhosis and/or liver cancer. In pediatric liver cancer cases, up to 34% \~ 95% are caused by HBV infection.
Although two major classes of drugs have been approved for the treatment of chronic hepatitis B in adults, and there are multiple guidelines worldwide for the management of HBV infection in adults, there is lack of guidelines specifically for the management of children with HBV infection. In addition, the treatment of chronic hepatitis B in children faced great difficulties due to the lack of evidence-based medical evidence for antiviral treatment of chronic hepatitis B in children and fewer drugs approved for anti-HBV treatment in children. The timing of treatment, medications, and clinical management strategies are all controversial.
This study ( Sprout project),is a multicenter, prospective, cohort study in China, aiming to explore and optimize the antiviral treatment regimen for children with HBV infection, to provide evidence-based medical for antiviral treatment, and to provide basis evidence for the standardized management of children infection with HBV in China. The study is expected to enroll 1900 pediatric patients with HBV infection, and patient will received one of the three following treatment Strategies: nucleoside monotherapy, peginterferon α- combined with nucleoside therapy, or peginterferon α-pulse therapy combined with nucleoside therapy, according to their illness state and desire, and the safety and efficacy will be evaluated.
1,656 studies on the registry are indexed under Hepatitis B; 196 are open to participants now.
This study's planned enrollment of 1,900 is above the median of 120 across 1,187 interventional studies indexed under Hepatitis B.
Browse Hepatitis B studies →Fang Wang is the lead sponsor of 4 studies on the registry; 3 are open to participants now.
Counted across the registry records on this site, refreshed daily.
1.Inclusion criteria for treatment-naïve children with hepatitis B:
2.Inclusion criteria for NA-treated children with hepatitis B:
3.Inclusion criteria for chronic HBV carrying children with normal ALT:
Exclusion Criteria:
Patients with contraindications to peginterferon alfa-2b, including but not limit to :
Drug: Peginterferon alfa-2b combined and ETV
Drug: Peginterferon alfa-2b combined and ETV
Drug: Peginterferon alfa-2b combined and ETV
Child patients are assigned to one of the 3 treatment regimens according to their illness state and treatment desire of their parents/guardians, and the number of patients in each group is expected to limited to 300. 1. NA monotherapy group : received entecavir (ETV) for 96 weeks. 2. Combination therapy group: received peginterferon alfa-2b combined with ETV for 96 weeks. 3. Pulse therapy group :received peginterferon alfa-2b pulse treatment combined with ETV for 144 weeks.
Clinical cure rate.
Defined as the proportion of child patients with HBsAg \< 0.05 IU / mL (or below the lower detection limit) 24 weeks after completing treatment, HBeAg negative, HBV DNA undetectable, and normalization of liver biochemical indexes (ALT and AST).
Time frame: 24 weeks after completing treatment.
Proportion of patients with HBV-DNA negative in those with HBV-DNA positive at baseline.
Defined as HBV-DNA below the lower detection limit, or\< 20 IU/mL.
Time frame: 24 weeks after treatment completion
HBeAg seroconversion rate in HBeAg positive children.
Defined as HBeAg negative and anti-HBe positive.
Time frame: 24 weeks after treatment completion.
HBsAg seroconversion rate.
Defined as HBsAg \< 0.05 IU/mL and anti-HBe positive.
Time frame: 24 weeks after treatment completion.
ALT normalization rate.
Time frame: 48 weeks and 96 weeks after starting treatment
Decrease of HBV-DNA compared to baseline.
Time frame: 24 weeks after treatment completion.
Decrease of HBeAg compared to baseline.
Time frame: 24 weeks after treatment completion.
Decrease of HBsAg compared to baseline.
Time frame: 24 weeks after treatment completion.
The incidence of adverse reactions.
Including fever, influenza-like symptoms, decreased hemogram, jaundice ALT\> 400U/L, abnormal renal function, abnormal thyroid function, abnormal blood phosphorus and blood calcium during treatment (lower or higher than the normal value).
Time frame: 24weeks ,48 weeks and 96 weeks after starting treatment
The effects on height
Time frame: 24weeks ,48 weeks and 96 weeks after starting treatment
The effects on weight
Time frame: 24weeks ,48 weeks and 96 weeks after starting treatment
The effects on bone age.
Time frame: 24weeks ,48 weeks and 96 weeks after starting treatment
Plan to share: No
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Fang Wang