Phase 2 Study of AHB-137 in HBeAg Negative Chronic Hepatitis B (CHB) Participants in Asia Pacific Region

Официальное название

A Phase 2 Multi-center, Randomized, Open-label Study to Assess the Efficacy and Safety of AHB-137 in Nucleos(t)Ide Analogue-treated Participants With HBeAg Negative Chronic Hepatitis B in the Asia Pacific Region

Обзор

This study is a randomized, open-label, multicenter phase 2 clinical trial to evaluate the efficacy and safety of AHB-137 injection in participants with HBeAg-negative CHB treated with Nucleos(t)ide Analogue (NAs).

Вмешательства

• Препарат AHB-137
  Subcutaneous injection

Первичные конечные точки

• Proportion of participants with sustained response post AHB-137 treatment [Срок оценки: 24 Weeks post AHB-137 treatment]

Вторичные конечные точки (12)

• Proportion of participants with functional cure (FC) or sustained HBV DNA response off all HBV treatment [Срок оценки: Off-treatment follow-up (Week 48 to 96)]
• Proportion of participants with functional cure (FC) [Срок оценки: Week 72]
• Proportion of participants with sustained HBV DNA response [Срок оценки: From baseline through Week 72]
• Proportion of participants with HBsAg ≤10 IU/mL and HBV DNA < Lower Limit of Quantification (LLOQ) post AHB-137 treatment [Срок оценки: 24 weeks post AHB-137 treatment]
• Proportion of participants with HBsAg <100 IU/mL and HBV DNA < LLOQ [Срок оценки: 24 weeks post AHB-137 treatment and at Week 72]
• Proportion of participants with complete response (CR) [Срок оценки: From baseline through end of study (Week 96)]
• Proportion of participants with HBsAg < or ≥ LOD (0.05 IU/mL) and/or HBV DNA < or ≥ LLOQ [Срок оценки: From baseline through end of study (Week 96)]
• Proportion of participants with ultrasensitive HBsAg < LOD (0.005 IU/mL) [Срок оценки: From baseline through end of study (Week 96)]
• Proportion of participants with HBsAg ≤ 10 IU/mL and < 100 IU/mL [Срок оценки: From baseline through end of study (Week 96)]
• Proportion of participants that meet nucleos(t)ide analog (NA) discontinuation criteria [Срок оценки: Week 48]
• Categorical change from baseline in serum hepatitis B surface antigen (HBsAg) levels, defined as reductions of ≥0.5, ≥1.0, ≥1.5, ≥2.0, or ≥3.0 log₁₀ IU/mL, assessed at each scheduled study visit [Срок оценки: From baseline through end of study (Week 96), assessed at each scheduled visit]
• Proportion of participants with anti-HBs seroconversion (with hepatitis B surface antibody [HBsAb] > 10 IU/L) [Срок оценки: Weeks 24, 48, and 72]

Критерии участия

Критерии включения

Participants are eligible to be included in the study only if all of the following criteria apply:

• Adults ≥18 years of age (or per local age of majority) and ≤65 years of age at Screening who are able to provide informed consent, comply with study procedures, and agree to discontinue nucleos(t)ide analog (NA) therapy if protocol-defined discontinuation criteria are met.
• Body mass index (BMI) ≤35 kg/m².
• Documented chronic hepatitis B virus (HBV) infection for ≥6 months prior to randomization, defined by hepatitis B surface antigen (HBsAg) positivity or detectable HBV DNA.
• Hepatitis B e antigen (HBeAg) negative at Screening.
• Receiving stable, approved nucleos(t)ide analog (NA) monotherapy for ≥6 months prior to randomization.
• HBV DNA below the lower limit of quantification (LLOQ) at Screening.
• Hepatitis B surface antigen (HBsAg) level >100 IU/mL and ≤3,000 IU/mL at Screening.
• Alanine aminotransferase (ALT) ≤2 × upper limit of normal (ULN) at Screening.
• Screening electrocardiogram (ECG) without clinically significant abnormalities and with a Fridericia-corrected QT interval (QTcF) ≤450 msec for males or ≤470 msec for females.
• Females of childbearing potential must not be breastfeeding and must have a negative serum pregnancy test at Screening and a negative urine pregnancy test prior to first dose.
• Male and female participants of childbearing potential must agree to use protocol-specified effective contraception during the dosing period and for ≥6 months after the last dose of AHB-137.

Критерии исключения

Participants will be excluded from the study if any of the following criteria apply:

• Clinically significant disease other than chronic hepatitis B virus (HBV) infection, as documented in medical history or identified on physical examination, including but not limited to acute coronary syndrome within 6 months prior to Screening, significant or unstable cardiac disease, uncontrolled diabetes, bleeding diathesis or coagulopathy, or prior solid organ or bone marrow transplant
• Concomitant clinically significant liver disease, including but not limited to viral hepatitis caused by other pathogens, hemochromatosis, Wilson's disease, primary biliary cholangitis, autoimmune liver disease, alcoholic liver disease, drug-induced liver injury, or current or prior history of clinical hepatic decompensation (e.g., ascites, encephalopathy, hepatorenal syndrome, or variceal hemorrhage).
• Any severe infection (other than chronic HBV infection) within 1 month prior to randomization and/or requiring intravenous anti-infective therapy.
• History of immune thrombocytopenia.
• Current suspected liver cirrhosis and/or evidence of cirrhosis defined as liver stiffness measurement (LSM) >9 kPa by FibroScan® or equivalent imaging modality (e.g., ultrasound elastography).
• History of liver cirrhosis defined by liver biopsy or by LSM >12 kPa by FibroScan® or equivalent imaging modality.
• Prior history of, current diagnosis of, or suspected hepatocellular carcinoma (HCC), or alpha-fetoprotein (AFP) ≥20 ng/mL at Screening.
• History of extrahepatic diseases potentially associated with HBV infection, including but not limited to nephrotic syndrome, any form of glomerulonephritis, polyarteritis nodosa, cryoglobulinemia, or uncontrolled hypertension.
• Laboratory evidence of active infection with human immunodeficiency virus (HIV), hepatitis C virus (HCV), hepatitis D virus (HDV), or active syphilis. Participants with positive HCV or HDV serology and documented negative HCV RNA or HDV RNA, respectively, are eligible.
• Abnormal laboratory values at Screening meeting any of the following criteria:

• Serum albumin <3.5 g/dL
• Estimated glomerular filtration rate (eGFR) <60 mL/min/1.73 m² calculated using the CKD-EPI equation (or JSN-CKDI equation for participants in Japan)
• International normalized ratio (INR) >1.25
• Platelet count <125 × 10⁹/L
• Total bilirubin >1.5 × upper limit of normal (ULN). Participants with benign unconjugated hyperbilirubinemia (Gilbert's syndrome) may be enrolled if deemed eligible by the Investigator
• Urine albumin-to-creatinine ratio (uACR) >0.3 mg/mg (300 mg/g) on two consecutive measurements following a positive or weakly positive urine protein result on routine urinalysis
• Borderline positive or positive antineutrophil cytoplasmic antibody (ANCA) results requiring further evaluation (MPO-ANCA and PR3-ANCA). Eligibility requires review of complete medical history and confirmation of no past or current vasculitic, inflammatory, or autoimmune disease by the Sponsor or Sponsor-designated Medical Monitor
• History of vasculitis or presence of signs or symptoms suggestive of vasculitis (e.g., vasculitic rash, skin ulceration, unexplained recurrent hematuria), or history or presence of diseases associated with vasculitis (e.g., systemic lupus erythematosus, rheumatoid arthritis, relapsing polychondritis, mononeuritis multiplex).
• History of malignancy within 5 years prior to Screening, except for adequately treated non-melanoma skin cancer. Participants currently undergoing evaluation for potential malignancy are excluded.
• History of hypersensitivity or allergy to any component of the investigational product (IP).
• Major trauma or major surgery within 3 months prior to Screening, or planned surgery during the study period unless eligibility is confirmed by the Medical Monitor.
• Current alcohol or substance abuse that, in the Investigator's judgment, may interfere with study participation or compliance.
• Female participants who are pregnant, breastfeeding, planning pregnancy during the study, or unwilling to refrain from egg donation and/or in vitro fertilization during the study.
• Participation in another clinical trial or receipt of any investigational product prior to first dose in this study within:

• Five half-lives (if known) or twice the duration of biological effect (if known), whichever is longer, or
• Six months, if neither half-life nor duration of effect is known
• Prior treatment with antisense oligonucleotides (ASOs) or small interfering RNA (siRNA)-based therapies.
• Any of the following prior or concomitant therapies:

• Prolonged use of immunomodulators (e.g., corticosteroids, methotrexate), cytotoxic drugs, or biologics (e.g., monoclonal antibodies) within 6 months prior to first IP administration, except for short-term treatment (≤2 weeks) or topical/inhaled corticosteroids
• Interferon therapy within 12 months prior to first dose
• Vaccination within 1 month prior to Screening, except for influenza or SARS-CoV-2 (COVID-19) vaccination or booster
• Current treatment with bulevirtide
• Requirement for long-term regular use of anticoagulants (e.g., warfarin, factor Xa inhibitors) or antiplatelet agents (e.g., clopidogrel or regular aspirin), except for low-dose aspirin, unless the Investigator determines the medication can be safely discontinued prior to first IP administration. Participants taking low-dose aspirin must agree to discontinue use during the study if protocol-specified conditions are met.
• Any other condition or circumstance that, in the Investigator's judgment, would make the participant unsuitable for participation in the study.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение

Рандомизированное

Модель

Параллельные группы

Маскирование

Открытое

Основная цель

Лечение

Центры проведения

Тайвань · 3 центра

• Chiayi Christian Hospital — Chiayi City
• E-DA Hospital — Kaohsiung City
• National Taiwan University Hospital — Taipei

Япония · 2 центра

• Japanese Red Cross Musashino Hospital — Musashino
• National Center for Global Health and Medicine — Shinjuku-Ku

Австралия · 1 центр

• St Vincents Hospital Melbourne — Fitzroy

Китай · 1 центр

• Queen Mary Hospital - PPDS — Гонконг

Новая Зеландия · 1 центр

• New Zealand Clinical Research — Grafton

Сингапур · 1 центр

• National University Hospital - Singapore — Singapore

South Korea · 1 центр

• Asan Medical Center — Seoul

Идентификаторы

NCT: NCT07370207 · AB-10-8011

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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