ConductScience.org, home

Trial · NCT07069569

A Multicenter Study of AHB-137 Injection Combined With Other Hepatitis B Drugs

NCT07069569, Phase 2, Recruiting, Ausper Biopharma Co., Ltd.

3 sourcestrials-2026-11-12-0.5.0

Download JSON
Cite this record

ConductScience Library. A Multicenter Study of AHB-137 Injection Combined With Other Hepatitis B Drugs. Trials, record NCT07069569. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07069569

On this page

Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
A Multicenter Study of AHB-137 Injection Combined With Other Hepatitis B Drugs
NCT number
NCT07069569
Status
Recruiting
Phases
Phase 2
Enrollment
200 participants, estimated
Lead sponsor
Ausper Biopharma Co., Ltd.
Conditions
Chronic Hepatitis B
Interventions
AHB-137, Peg-IFN, Hepatitis B Vaccine
First posted
2025-07-16
Last updated
2026-07-29

Source ClinicalTrials.gov

Registered outcomes16

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryProportion of participants with persistent HBsAg < limit of detection (LOD) and HBV DNA < lower limit of quantification (LLOQ) at the 24th week after all treatment for CHB was discontinued.up to 72 weeks
SecondaryProportion of participants with persistent HBsAg < LOD and HBV DNA < LLOQ .Up to 72 weeks
SecondaryDetection of the serum concentration of HBsAg, HBsAb, HBV DNA, HBV RNA, HBcrAg, HBeAb,and HBeAg.Up to 72 weeks
SecondaryProportion of participants who met discontinuation criteria for NAs treatment at the end of the treatment period.Up to 48 weeks
SecondaryRelapse rate after discontinuation of NAs therapy.Up to 72 weeks
SecondaryChange from baseline in alanine aminotransferase (ALT) values and time to normalization of values.Up to 72 weeks
SecondaryRelapse time after discontinuation of NAs therapy.Up to 72 weeks
SecondaryPlasma concentrations of AHB-137.Up to 48 weeks
SecondarySerum concentrations of Peg-IFN.Up to 48 weeks.
SecondarySafety: Number and percentage of participants with detectable anti-drug antibodies (ADA).Up to 72 weeks

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT07069569

GET https://conductscience.org/api/trials/v1/NCT07069569/registered