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A Randomized, Open-Label, Multicenter Phase II Study to Evaluate the Efficacy and Safety of AHB-137 Injection in Combination With Hepatitis B Vaccine or Pegylated Interferon α-2b (Peg-IFN) in Participants With HBeAg-Negative Chronic Hepatitis B (CHB) Treated With Nucleos(t)Ide Analogue (NAs)

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This is a randomized, open-label, multicenter phase II study to evaluate the efficacy and safety of AHB-137 injection in combination with other hepatitis B drugs in participants with HBeAg-negative CHB treated with NAs.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• Participants voluntarily participate in the study, and sign the Informed Consent Form (ICF) prior to screening, able to complete the study according to the protocol;

• Aged between 18 and 65 years at the time of signing the ICF;

• Body mass index (BMI) within the range of 18-30 kg/ m2;

• HBeAg negative at screening;

• HBsAg or HBV DNA positive for at least 6 months;

• Continue antiviral therapy with a single nucleoside (t) ide analogue for more than 6 months prior to screening;

• Alanine aminotransferase (ALT) ≤ 2 × upper limit of normal (ULN);

• Effective contraception as required.

Locations
Other Locations
China
Beijing Friendship Hospital, Capital Medical University
RECRUITING
Beijing
Contact Information
Primary
Lu
clinicaltrial@ausperbio.com
0571-86959519
Time Frame
Start Date: 2025-06-08
Estimated Completion Date: 2028-01-15
Participants
Target number of participants: 200
Treatments
Experimental: AHB-137 (16 weeks) and Peg-IFN
Experimental: AHB-137 (24 weeks) and Peg-IFN
Experimental: AHB-137 and Hepatitis B vaccine
Experimental: AHB-137
Experimental: AHB-137 (24 weeks) and Peg-IFN(24 weeks)
R3 group
Related Therapeutic Areas
Sponsors
Leads: Ausper Biopharma Co., Ltd.

This content was sourced from clinicaltrials.gov