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NCT07137910RecruitingPhase 2

A Study to Evaluate the Efficacy and Safety of AHB-137 Injection in Participants With Chronic Hepatitis B (CHB)

An Open-Label, Multicenter, Phase 2 Study to Evaluate the Efficacy and Safety of AHB-137 Injection in Participants With Low-HBsAg Chronic Hepatitis B

Source: ClinicalTrials.gov · Last updated 5 Aug 2026

Brief summary (registry, in English)

This is an open-label, multicenter, Phase 2 study designed to evaluate the efficacy and safety of AHB-137 injection in participants with chronic hepatitis B (CHB) with low hepatitis B surface antigen (HBsAg) levels.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
200 (estimated)
First submitted
15 Aug 2025
Start date
4 Sept 2025
Primary completion date
12 Dec 2026
Lead sponsor
Ausper Biopharma Co., Ltd.
Diseases
Hepatitis B
NCT number
NCT07137910

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 200
  • From 4 Sept 2025 to the primary completion date, 12 Dec 2026
  • 11 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Participants with recent major trauma or major surgery, or planning surgery;
  • Those who are participating in another clinical trial, or have not undergone a protocol-specified washout period prior to this study;
  • Prior/current use of prohibited medications;

Other illness

  • Uncontrolled and stable clinically significant abnormalities other than a history of CHB infection;
  • Associated liver disease;
  • Any serious infection other than CHB infection requires intravenous anti-infective therapy;
  • HCV RNA positive, HIV antibody positive, syphilis positive;
  • Diseases associated with vascular inflammatory conditions;
  • History of malignancy or ongoing assessment of possible malignancy;
  • History of allergies, or allergic constitution;

Lab values

  • Abnormal laboratory results;
  • QT interval corrected heart rate (Fridericia method) abnormal;

Other

  • Inappropriate for participation in this trial as judged by the investigator.

Who the study is looking for

  • Voluntarily participate in the study and sign the informed consent form;
  • 18-65 years of age (including boundary values) ;
  • Body mass index met the requirements;
  • Participants with CHB who are HBsAg or HBV DNA positive for at least 6 months;
  • Meet the relevant requirements for prior medications;
  • HBsAg and HBV DNA and liver function indicators meet the requirements;
  • Effective contraception as required;

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (11)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
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BeijingChinaRecruiting
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ChangzhouChinaNot yet recruiting
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ChengduChinaNot yet recruiting
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ChongqingChinaNot yet recruiting
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GuangzhouChinaNot yet recruiting
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HangzhouChinaNot yet recruiting
-
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Jilin CityChinaRecruiting
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Coordinator of this site? Confirm its status
NanningChinaRecruiting
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Coordinator of this site? Confirm its status
ShenzhenChinaNot yet recruiting
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Coordinator of this site? Confirm its status
XiamenChinaRecruiting
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Coordinator of this site? Confirm its status
ZhengzhouChinaNot yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.