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RecruitingNCT05792761Updated Mar 31, 2023

A Study on Antiviral Treatment of Chronic Hepatitis B in Children

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

From the registry’s dates

  • Primary completion was expected by Dec 2025, 9 months ago, but the record still lists the study as recruiting.
  • Registered 1 year 9 months after the study started (first participant enrolled May 2021, registered Feb 2023).
  • Started May 2021; still recruiting 5 years 5 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
1,900
Allocation
Non-randomized
Ages
3 Years to 18 Years
Sex
All
01

Study summary

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.

02

Conditions studied

  • Chronic HBV Infection
03

In context

Hepatitis B

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 →

Lead sponsor

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.

04

Who can participate

Ages eligible
3 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

1.Inclusion criteria for treatment-naïve children with hepatitis B:

  1. Aged 3 to 18 (included 3 years old, but exclude 18 years old);
  2. HBV DNA positive (higher than the lower detection limit or >20 IU/ml. Roche reagent is recommended).
  3. HBsAg positive (higher than lower detection limit or >0.05 IU/ml. Roche reagent is recommended).
  4. ALT flares between 1 to10 ULN at least twice a year. If the last examination result is higher than 5ULN, the investigator shall comprehensively judge whether the child patient is suitable to participate in this study.
  5. The guardian should understand and sign the informed consent form (if parents is the legal guardians, they both must sign the informed consent form). Children older than 8 years (included) also must sign the informed consent form. The consent comment of child patient under the age of 8 should also be clearly recorded.

2.Inclusion criteria for NA-treated children with hepatitis B:

  1. Aged 3 to 18 (included 3 years old, but exclude 18 years old);
  2. Previously received NA treatment for ≥ 1 year.
  3. HBsAg positive (higher than lower detection limit or >0.05 IU/ml. Roche reagent is recommended).
  4. The guardian should understand and sign the informed consent form (if parents is the legal guardians, they both must sign the informed consent form). Children older than 8 years (included) also must sign the informed consent form. The consent comment of child patient under the age of 8 should also be clearly recorded.

3.Inclusion criteria for chronic HBV carrying children with normal ALT:

  1. Aged 3 to 18 (included 3 years old, but exclude 18 years old);
  2. HBV DNA positive (higher than lower detection limit or >20 IU/ml. Roche reagent is recommended).
  3. HBsAg positive (higher than lower detection limit or >0.05 IU/ml. Roche reagent is recommended).
  4. Serum ALT and AST remain persistently normal (2 consecutive follow-up visits within half a year, with an interval of at least 3 months)
  5. TThe guardian should understand and sign the informed consent form (if parents is the legal guardians, they both must sign the informed consent form). Children older than 8 years (included) also must sign the informed consent form. The consent comment of child patient under the age of 8 should also be clearly recorded.

Exclusion criteria

Exclusion Criteria:

  1. Co-infected with HAV, HCV, HDV, HEV or HIV.
  2. Patients with contraindications to peginterferon alfa-2b, including but not limit to :

    1. Hepatitis B cirrhosis decompensated stage.
    2. Child patient with autoimmune liver disease, metabolic liver disease or alcoholic liver disease; malignant tumor, decompensated liver disease, or organ transplantation.
    3. Child patient with severe neurological or mental disorders.
    4. Child patient with severe hyperthyroidism or other autoimmune disorders.
    5. Child patient with diabetes under poorly controlled.
    6. Child patient with retinal or fundus lesions.
    7. Child patient with severe heart disease, coronary heart disease or cerebrovascular disease.
    8. Child patient with poorly controlled epilepsy.
  3. Child patient with severe renal dysfunction, e.g. creatinine > 1.5 ULN.
  4. Child patient who in the opinion of the investigator is unsuitable for enrollment.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
1,900 participants (estimated)

Study arms

  • Experimental
    treatment-naïve children with hepatitis B

    Drug: Peginterferon alfa-2b combined and ETV

  • Experimental
    previously treated children with hepatitis B

    Drug: Peginterferon alfa-2b combined and ETV

  • Experimental
    chronic HBV carrying children with normal ALT

    Drug: Peginterferon alfa-2b combined and ETV

Interventions

  • DrugPeginterferon 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.

06

What researchers measure

Primary outcomes

  1. 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.

Secondary outcomes

  1. 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

  2. HBeAg seroconversion rate in HBeAg positive children.

    Defined as HBeAg negative and anti-HBe positive.

    Time frame: 24 weeks after treatment completion.

  3. HBsAg seroconversion rate.

    Defined as HBsAg \< 0.05 IU/mL and anti-HBe positive.

    Time frame: 24 weeks after treatment completion.

  4. ALT normalization rate.

    Time frame: 48 weeks and 96 weeks after starting treatment

  5. Decrease of HBV-DNA compared to baseline.

    Time frame: 24 weeks after treatment completion.

  6. Decrease of HBeAg compared to baseline.

    Time frame: 24 weeks after treatment completion.

  7. Decrease of HBsAg compared to baseline.

    Time frame: 24 weeks after treatment completion.

  8. 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

  9. The effects on height

    Time frame: 24weeks ,48 weeks and 96 weeks after starting treatment

  10. The effects on weight

    Time frame: 24weeks ,48 weeks and 96 weeks after starting treatment

  11. The effects on bone age.

    Time frame: 24weeks ,48 weeks and 96 weeks after starting treatment

07

Study locations

1 of 1 sites recruiting
  • Shenzhen Third People Hospital
    Shenzhen, China
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 31, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05792761
Lead sponsor
Fang Wang
Responsible party
Fang Wang (Chief physician, Shenzhen Third People's Hospital) — Sponsor-investigator
First posted
Mar 31, 2023
Start date
May 6, 2021
Primary completion
Dec 31, 2025 (estimated)
Completion
Dec 31, 2025 (estimated)
Last update
Mar 31, 2023

Study contacts

Fang Wang
Contact
kaixin919@163.com
+8613682662543
Qing He
principal investigator · Shenzhen Third People's Hospital
Hongfei Zhang
principal investigator · Beijing Tsinghua Changgeng Hospital
Fang Wang
study chair · Shenzhen Third People's Hospital

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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