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NCT Number: NCT07307586

A Small Sample Prospective Clinical Study of Azvudine Tablets to Promote Clinical Cure in Patients With Chronic Hepatitis B

Through regular monitoring of viral load, liver function and immune cell activity, the long-term efficacy of Adefovir in controlling HBV is precisely evaluated. By employing a dual mechanism of "antiviral action plus immune activation", it offers a novel therapeutic option for achieving clinical cure in chronic hepatitis B.

Recruiting

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

The First Affiliated Hospital of Zhengzhou University

Zhengzhou, Henan, 450052, China

Location status: Recruiting

Location contact

Zhigang Ren, Dr.

CONTACT

[email protected]

+8618703636245

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All subjects must meet the following criteria to be eligible for inclusion in the trial:
  • Meet the diagnostic criteria for viral hepatitis as outlined in the Chinese Medical Association's Hepatology Branch Guidelines for the Prevention and Treatment of Chronic Hepatitis B, with patients demonstrating sustained positivity for hepatitis B e antigen (HBeAg) and hepatitis B surface antigen (HBsAg) for at least six months;
  • HBV DNA load > 20,000 copies/mL and HBsAg < 1,500 IU/mL;
  • Serum alanine aminotransferase (ALT) > 2 times the upper limit of normal;
  • No prior antiviral therapy prior to hospital admission.

Exclusion criteria

  • All subjects meeting any of the following criteria shall be excluded from this study:
  • Individuals co-infected with other hepatotropic viruses, such as hepatitis A, C, D, or E viruses, or HIV;
  • Patients with concomitant liver metabolic disorders, cirrhosis, autoimmune-related diseases, or other chronic conditions;
  • Pregnant or breastfeeding women, or those planning pregnancy within one year;
  • Patients who have received or are currently undergoing antineoplastic therapy;
  • History of alcohol or substance abuse;
  • Patients currently taking therapeutic medications or health supplements;
  • Patients who participated in other clinical trials within 30 days prior to enrolment;
  • Patients with allergic constitutions or hypersensitivity to any drug or component used in this study;
  • Patients with gastrointestinal disorders that may impair drug absorption.

Treatment and study plan

Azvudine

Drug

CHB patients with Azvudine treatment

TAF

Drug

CHB patients with TAF treatment

IFNα-2a

Drug

CHB patients with IFNα-2a treatment

Primary outcomes

  1. Follow-up at 12 months

    Time frame: 12 month

    Taking the medication orally for 12 months.

Secondary outcomes

  1. Adverse events

    Time frame: Up to 30 days (form the date of confirmed CHB)

    Discontinuation of medication due to adverse events or other reasons

Study contacts

Contact information is provided by the study sponsor or research team.

Zhigang Ren, Dr.

CONTACT

[email protected]

+8618703636245

Sponsors and collaborators

Lead sponsor

Zhigang Ren

Other

Registry information

Official study title

A Small Prospective Clinical Study on Azvudine Tablets for Treating Chronic Hepatitis B.

Important dates

Study start
2025
Primary completion
2026
Study completion
2027
First posted
Dec 29, 2025
Registry last updated
Dec 29, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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