ClinicalTrials.gg
RecruitingNCT07630727Updated Jul 21, 2026

Study of AHB-171 in Chronic Hepatitis B Participants

A Phase 2 interventional study of AHB-171 Injection in Hepatitis B, Chronic (CHB), sponsored by Ausper Biopharma Co., Ltd.. Recruiting at 10 sites in China. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-07-21.

Sponsored by Ausper Biopharma Co., Ltd. · Phase 2, Interventional, and Treatment

From the registry’s dates

  • Started Jun 2026; still recruiting 4 months later.
Phase
Phase 2
Study type
Interventional
Enrollment
138
Allocation
Non-randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

The study adopts an open-label, multiple-dose design and aims to evaluate the efficacy and safety of AHB-171 Injection after multiple doses in treatment-naïve (HBeAg-negative/positive) and nucleos(t)ide analogue (NA)-treated (HBeAg-negative) participants with chronic hepatitis B (CHB)

02

Conditions studied

  • Hepatitis B, Chronic (CHB)
03

In context

Hepatitis B

1,045 studies on the registry are indexed under Hepatitis B; 139 are open to participants now.

This study's planned enrollment of 138 is close to the median of 147 across 756 interventional studies indexed under Hepatitis B.

Browse Hepatitis B studies →

Lead sponsor

Ausper Biopharma Co., Ltd. is the lead sponsor of 14 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 65 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

  • Able to fully understand and sign the form (ICF).
  • Male or female participants, aged 18-65 years (inclusive).
  • (BMI) meeting the predefined eligibility range.
  • Chronic (CHB) participants with HBsAg or HBV DNA positivity for ≥6 months at screening.
  • At screening, participants meeting predefined ranges of HBsAg, HBV DNA, and according to prior nucleos(t)ide analogue (NA) treatment history (stable prior treatment or treatment-naive), and meeting corresponding prior antiviral treatment duration requirements.
  • Adopt effective measures as required

Exclusion criteria

Exclusion Criteria:

  • History of any severe systemic disease or other than chronic infection which, in the opinion of the investigator, makes the subject unsuitable for study participation.
  • Prior history of solid organ or hematopoietic stem cell transplantation.
  • History of any other liver disease that the investigator considers unsuitable for trial.History of disease or diseases with potential immune activation risk.
  • History or presence of hepatic decompensation at screening.
  • History of primary liver cancer, or diagnosis/suspected liver cancer at screening.
  • Imaging or histological evidence of significant liver fibrosis or cirrhosis within 12 months prior to screening, or a liver stiffness measurement indicative of significant fibrosis or cirrhosis at screening. Major trauma or major surgery within 12 weeks prior to screening
  • History of severe allergies (e.g., to ≥2 allergens) or severe allergy to any component of the study drug, or in the opinion of the investigator, makes the subject unsuitable for participation.
  • Severe infection requiring intravenous anti-infective therapy within 2 weeks prior to screening (excluding chronic HBV infection).
  • History of drug abuse, or alcoholism.
  • Blood donation or blood loss exceeding the specified volume within 12 weeks prior to screening, or planned blood donation during the trial period.
  • Use of , immunomodulators, cytotoxic drugs, or biologics within 6 months prior to screening.
  • Use of any oligonucleotide drugs or interferon therapy within 12 months prior to screening.
  • Vaccination within 4 weeks prior to screening, or planned vaccination during the trial period.
  • Presence of tattoos, active skin diseases, or other conditions that may interfere with subcutaneous drug administration or observation of injection site reactions.
  • abnormal (ECG) at screening.
  • Tested positive for , or active syphilis infection.
  • Uncontrolled hypertension at screening.
  • Clinically significant abnormal laboratory test as specified in protocol at screening.
  • Currently participating in another clinical trials, or within the .
  • Any other condition or factor which, in the opinion of the investigator, makes the subject unsuitable for trial participation.
Terms in these criteria, in plain language(13)

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.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

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.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

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.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

ECG (electrocardiogram)

A recording of the heart’s electrical activity, taken with stickers on the chest, arms and legs. It takes a few minutes and does not hurt.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

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.

Washout period

A planned gap after a treatment, so that its effects can lessen before the study treatment or a study assessment. Ask the study team and the doctor who prescribed it before changing any medicine.

05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
138 participants (estimated)

Study arms

  • Experimental
    AHB-171 in Treatment CHB

    Drug: AHB-171 Injection

  • Experimental
    AHB-171 in Naïve CHB

    Drug: AHB-171 Injection

Interventions

06

What researchers measure

Primary outcomes

  1. Proportion of participants with HBsAg <10 IU/mL and HBV DNA < LLOQ (10 IU/mL)

    Time frame: Up to 90 days

Secondary outcomes

  1. Proportion of participants achieving complete response (HBsAg <0.05 IU/mL and HBV DNA < LLOQ)

    Time frame: Up to 90 days

  2. Change of HBsAg (log₁₀ IU/mL) from baseline and maximum reduction at each visit

    Time frame: Up to 90 days

  3. Proportion of participants with HBsAg decline from baseline of <0.5, ≥0.5, ≥1.0, ≥1.5, ≥2.0, ≥3.0 log₁₀ IU/mL at each visi

    Time frame: Up to 90 days

  4. Proportion of participants with HBsAg <100 IU/mL, <10 IU/mL, <1 IU/mL at each visit

    Time frame: Up to 90 days

  5. Proportion of participants achieving HBsAg clearance (HBsAg <0.05 IU/mL) at each visit

    Time frame: Up to 90 days

  6. Proportion of participants with HBV DNA < LLOQ (10 IU/mL) at each visit

    Time frame: Up to 90 days

  7. Proportion of participants achieving complete response (HBsAg <0.05 IU/mL and HBV DNA < LLOQ) at each visit

    Time frame: Up to 90 days

  8. Proportion of participants with anti-HBs seroconversion (HBsAg clearance and HBsAb >10 IU/L) at each visit

    Time frame: Up to 90 days

  9. Absolute or log change from baseline for HBsAg at each visit

    Time frame: Up to 90 days

  10. Absolute or log change from baseline for HBV RNA at each visit

    Time frame: Up to 90 days

  11. Absolute or log change from baseline for HBcrAg at each visit

    Time frame: Up to 90 days

  12. Absolute or log change from baseline for HBeAg at each visit

    Time frame: Up to 90 days

  13. Absolute or log change from baseline for HBeAb at each visit

    Time frame: Up to 90 days

  14. Proportion of participants with baseline ALT > ULN achieving ALT normalization, and time to ALT normalization

    Time frame: Up to 90 days

  15. Incidence and severity of treatment-emergent adverse events (TEAE) and serious adverse events (SAE)

    CTCAE will be used to describe severity.

    Time frame: Up to 90 days

  16. Proportion of participants with clinically significant abnormalities in laboratory tests

    Time frame: Up to 90 days

  17. Proportion of participants with clinically significant abnormalities in ECG

    Time frame: Up to 90 days

  18. Proportion of participants with clinically significant abnormalities in physical examinations and vital signs

    Time frame: Up to 90 days

  19. Changes in ECG from baseline

    Time frame: Up to 90 days

  20. Proportion of participants with HBsAg decline ≥2.0 log₁₀ IU/mL

    Time frame: Up to 90 days

  21. Plasma concentration of AHB-171 at different time points

    Time frame: Up to 90 days

  22. Proportion of participants with detectable anti-drug antibody (ADA)

    Time frame: Up to 90 days

07

Study locations

10 of 10 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jun 2026 (actual). Primary completion is estimated for Mar 2029, 33 months after the start.

Of 40 industry-sponsored phase 2 interventional studies under Hepatitis B, half reached primary completion within 33 months of starting (the median), counting those still running; a quarter within 19 and three quarters within 40. This study's planned 33 months is close to that.

Counting every sponsor, half of 50 studies reached it within 30 months; a quarter within 19 and three quarters within 40.

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

Registered
Jun 2, 2026
First posted
Jun 5, 2026
StartActual
Jun 24, 2026
Primary completionEst.
Mar 31, 2029
CompletionEst.
May 31, 2029
Last update
Jul 21, 2026
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 Jul 21, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07630727
Responsible party
Sponsor
First posted
Jun 5, 2026
Start date
Jun 24, 2026
Primary completion
Mar 31, 2029 (estimated)
Completion
May 31, 2029 (estimated)
Last update
Jul 21, 2026

Study contacts

Bella Lu
Contact
clinicaltrial@ausperbio.com
0571-86959519

Oversight

Data monitoring committee
No
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: AHB-171

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