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Status unknownNCT05203055Updated Jan 24, 2022

Peginterferon Alpha-2b Therapy in Chronic Hepatitis Patients With Normal ALT Level and Low Viremia

A Phase 1/2 interventional study of Peginterferon alpha-2b and Nucleotide Analog in Chronic Hepatitis B Patients With a Normal ALT Level and Low Viremia, sponsored by Fuzhou General Hospital. Status unknown at 1 site in China. Open to participants aged 18 Years to 60 Years. Per ClinicalTrials.gov, last updated 2022-01-24.

Sponsored by Fuzhou General Hospital · Phase 1/2, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Dec 2021), so the status shown — last known as Recruiting — may be out of date.
Phase
Phase 1/2
Study type
Interventional
Enrollment
300
Allocation
Randomized
Ages
18 Years to 60 Years
Sex
All
01

Study summary

To date, antiviral treatment is not recommended for chronic hepatitis B patients with a normal ALT level and low viremia. The strategy is to closely monitor the patients. However, evidence suggests that these group are at risk of gradual disease progression and development of hepatocellular carcinoma. Peginterferon eliminates the hepatitis B virus through immune regulation and induction of antiviral protein expression. For patients with low viral load, the clinical cure rate is potentially promising. In this study, we aim to investigate the efficacy and safety of peginterferon alpha-2b therapy in selected chronic hepatitis B patients with normal ALT level and low viremia. It is expected to obtain a satisfactory curative effect. Peginterferon is a marketed drug available in Chinese clinics with indications of anti-hepatitis B virus.

02

Conditions studied

  • Chronic Hepatitis B Patients With a Normal ALT Level and Low Viremia
03

In context

Hepatitis B, Chronic

895 studies on the registry are indexed under Hepatitis B, Chronic; 151 are open to participants now.

This study's planned enrollment of 300 is above the median of 100 across 659 interventional studies indexed under Hepatitis B, Chronic.

Browse Hepatitis B, Chronic studies →

Lead sponsor

Fuzhou General Hospital is the lead sponsor of 40 studies on the registry; 9 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. willing to receive the treatment and sign ;
  2. 18-60 years old (including 18 and 60), both gender;
  3. positive for at least 6 months and \<1500IU/ml;
  4. ≤1xULN and no elevated ALT has been detected in history;
  5. HBV DNA detectable but\<2000 IU/ml;
  6. HBeAg negative ;

Exclusion criteria

Exclusion Criteria:

  1. For female participants: positive pregnancy test, presently breast-feeding, or unwillingness to use effective measures for the duration of the study. For male participants: intent to procreate 3 months before or after the intervention or unwillingness to use effective measures of the contraception ;
  2. neuropsychiatric diseases, such as depression, anxiety, mania, schizophrenia, or a family history of mental illness (especially with a history of depression or depression tendency);
  3. co-infection of , EBV, other hepatotropic viruses , non-hepatotropic viruses;
  4. alcoholic hepatitis, drug-induced hepatitis, liver disease;
  5. Patients with moderate to severe steatohepatitis;
  6. possibility of liver cirrhosis that cannot be excluded
  7. hepatocellular carcinoma or AFP level>30ng/ml;
  8. Kidney diseases: acute and chronic nephritis, renal insufficiency, nephrotic syndrome, serum creatinine> 1 x at the time of screening;
  9. at screening, the is less than 1.5×10\^9/L, and the count is less than 90×10\^9/L;
  10. Serum phosphorus level \<0.7 mmol/L;
  11. Antinuclear antibody (ANA)>1:100;
  12. Autoimmune diseases, including thyroiditis, psoriasis and systemic lupus erythematosus;
  13. Endocrine system diseases, including thyroid diseases and diabetes mellitus;
  14. Uncontrolled blood pressure: SBP>160 mmHg or DBP >100 mmHg at the time of enrollment;
  15. Evidence of cardiovascular disease, existing congestive cardiac failure on physical exam and/or acute coronary syndrome in the past 6 months;
  16. Severe retinopathy or other serious eye diseases;
  17. Organic disease or dysfunction;
  18. plan to receive an organ transplant or have already undergone an organ transplant;
  19. received standardized treatment with interferon or NA products before .
  20. allergic to interferon or pharmaceutical , or meet any of the in the experimental drug instructions;
  21. Participated in other interventional trials within 3 months before the screening or other conditions deemed unsuitable by the investigator.
Terms in these criteria, in plain language(11)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

ALT and AST (liver enzymes)

Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.

Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

ULN (upper limit of normal)

The top of the normal range for a blood test, as set by the laboratory that runs it. Each lab prints its own range next to your result.

“≤ 2.5 × ULN” means the result can be up to two and a half times that top value.

Absolute neutrophil count (ANC)

The number of neutrophils, white blood cells that help fight infection, in a given amount of blood. Too few raises the risk of infection.

It is a count, not a percentage of the white cells. Limits are written in units that mean the same: ≥ 1.5 × 10⁹/L is ≥ 1,500 per mm³ (µL). Each lab has its own reference range.

Platelets

Blood cells that help blood clot. Too few raises the risk of bleeding and bruising. A usual adult range is about 150–400 × 10⁹/L (150,000–400,000 per µL); each lab has its own reference range.

Excipients

The other ingredients in a medicine besides the active drug, such as fillers, colours or preservatives.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

05

Study design

Phase
Phase 1 / Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
300 participants (estimated)

Study arms

  • Experimental
    monotherapy group

    Peginterferon alpha-2b injection is given subcutaneously at a dosage of 180μg/w for 48 consecutive weeks. Patients will stop the treatment whenever HBsAg is eliminated, and those without HBsAg elimination after 48 dosages will enter the group of best treatment. The patients will be followed up for another 24 weeks after treatment.

    Drug: Peginterferon alpha-2b

  • Experimental
    continuous combination therapy group

    Peginterferon alpha-2b injection is given subcutaneously at a dosage of 180μg/w for 48 consecutive weeks, plus continuous oral NA. Patients will stop the treatment whenever HBsAg is eliminated, and those without HBsAg elimination after 48 dosages will enter the group of best treatment. The patients will be followed up for another 24 weeks after treatment.

    Drug: Peginterferon alpha-2b · Drug: Nucleotide Analog

  • Experimental
    pulse combination therapy group

    Peginterferon alpha-2b injection is given subcutaneously at a dosage of 180μg/w for 8 consecutive weeks and cessation for 4 weeks,plus continuous oral NA. Patients will discontinue the treatment at any time if they are recovery, and those without HBsAg elimination after 48 dosages will enter the group of best treatment.The patients will be followed up for another 24 weeks after treatment.

    Drug: Peginterferon alpha-2b · Drug: pulse peginterferon alpha-2b

Interventions

  • 180μg/w

  • DrugNucleotide Analog

    Etecavir 0.5mg qd or Tenofovir 300mg qd

  • Drugpulse peginterferon alpha-2b

    180μg/w for 8 consecutive weeks and cessation for 4 weeks

06

What researchers measure

Primary outcomes

  1. The percentage of patients with undetectable HBV DNA

    Time frame: week 24

  2. HBsAg clearance rate

    Time frame: week 48

  3. HBsAg conversion rate

    Time frame: week 48

Secondary outcomes

  1. The percentage of patients with undetectable HBV DNA

    Time frame: week 24 and week 48

  2. The HBsAg level

    Time frame: week 24 and week 48

  3. The HBV pgRNA level

    Time frame: week 24 and week 48

07

Study locations

1 of 1 sites recruiting
  • Fuzhou General Hospital, Xiamen Univ
    Fuzhou, Fujian 350025, China
    Recruiting
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Dec 2021 (actual). Primary completion is estimated for Dec 2022, 12 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Dec 18, 2021
First posted
Jan 24, 2022
StartActual
Dec 10, 2021
Primary completionEst.
Dec 10, 2022
CompletionEst.
Dec 10, 2023
Last update
Jan 24, 2022
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jan 24, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05203055
Lead sponsor
Fuzhou General Hospital
Responsible party
Sponsor
First posted
Jan 24, 2022
Start date
Dec 10, 2021
Primary completion
Dec 10, 2022 (estimated)
Completion
Dec 10, 2023 (estimated)
Last update
Jan 24, 2022

Study contacts

Dongliang Li, Professor
Contact
dongliangli93@163.com
008613665052006

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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Studies of the drug tested here: Peginterferon alfa-2b

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