Study of AHB-137 in Chronic Hepatitis B (CHB) Participants in North America and Europe Regions (ASPIRE-202)
2026年8月24日 更新者:AusperBio Therapeutics Inc.
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 Chronic Hepatitis B in the North America and Europe Regions
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 CHB treated with Nucleos(t)ide Analogue (NAs).
研究概览
研究类型
介入性
注册 (估计的)
70
阶段
- 阶段2
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习联系方式
- 姓名:Maggie Davis
- 电话号码:(650) 650-2877
- 邮箱:ausperbioclinicaltrials@ausperbio.com
学习地点
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Alberta
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Calgary、Alberta、加拿大、T2N 4N1
- 尚未招聘
- University Of Calgary
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Ontario
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Toronto、Ontario、加拿大、M5G 2C4
- 尚未招聘
- Toronto General Hospital
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Milan
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Milan、Milan、意大利、20122
- 尚未招聘
- Clinica Mangiagalli
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Clichy、法国、92118
- 尚未招聘
- Hopital Beaujon
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California
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Palo Alto、California、美国、94304-1509
- 尚未招聘
- Stanford University
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Maryland
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Baltimore、Maryland、美国、21201-1009
- 尚未招聘
- University of Maryland
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New York
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New York、New York、美国、10016
- 尚未招聘
- NYU Langone Health
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Texas
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San Antonio、Texas、美国、78215-2100
- 招聘中
- Texas Liver Institute
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London
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London、London、英国、SE5 9RS
- 尚未招聘
- King's College Hospital
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Barcelona
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Barcelona、Barcelona、西班牙、8035
- 尚未招聘
- Vall d'Hebron Hospital
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参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
不
描述
Inclusion Criteria:
Participants are eligible to be included in the study only if all of the following criteria apply:
- Adults ≥18 years of age and up to 65 years of age (inclusive) 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.
- Receiving stable, approved nucleos(t)ide analog (NA) monotherapy for ≥6 months prior to randomization.
- HBV DNA meeting protocol-specified virologic criteria at Screening.
- Hepatitis B surface antigen (HBsAg) level meeting protocol-specified virologic criteria at Screening.
- Alanine aminotransferase (ALT) meeting protocol-specified criteria 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.
- Males 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.
Exclusion Criteria:
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.
- Concomitant clinically significant liver disease.
- Any severe infection (other than chronic HBV infection) within 1 month prior to randomization.
- History of immune thrombocytopenia.
- Current suspected liver cirrhosis and/or evidence of cirrhosis by protocol-specified criteria for FibroScan® or equivalent imaging modality (e.g., ultrasound elastography); historical FibroScan® (or equivalent) results with documentation within 6 months from screening is acceptable.
- History of liver cirrhosis defined by liver biopsy or by FibroScan® or equivalent imaging modality using protocol-specified criteria.
- 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.
- 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.
- Protocol-specified abnormal laboratory values at Screening.
- History of vasculitis or presence of signs or symptoms suggestive of vasculitis, or history or presence of diseases associated with vasculitis.
- 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 judged by the Investigator to potentially interfere with participant 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.
- Any other condition or circumstance that, in the Investigator's judgment, would make the participant unsuitable for participation in the study.
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
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实验性的:Arm A: Dose Regimen A
Participants receive AHB-137 according to dosing regimen A.
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皮下注射
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实验性的:Arm B: Dose Regimen B
Participants receive AHB-137 according to dosing regimen B.
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皮下注射
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研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
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Proportion of participants with persistent HBsAg < limit of detection (LOD) and HBV DNA < lower limit of quantification (LLOQ)
大体时间:24 Weeks post AHB-137 treatment (Week 48)
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24 Weeks post AHB-137 treatment (Week 48)
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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符合核苷(酸)类似物(NA)停药标准的参与者比例
大体时间:第48周
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第48周
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抗-HBs血清转换(乙型肝炎表面抗体[HBsAb] > 10 IU/L)的参与者比例
大体时间:第24、48和72周
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第24、48和72周
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经历病毒学复发的参与者比例
大体时间:从基线期至第72周
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从基线期至第72周
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AHB-137的血浆浓度-时间曲线下面积(AUC)
大体时间:从首次给药(第1天)至药代动力学采样结束(第48周)
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从首次给药(第1天)至药代动力学采样结束(第48周)
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AHB-137给药间隔末期的浓度(Ct)
大体时间:从首次给药(第1天)至药代动力学采样结束(第48周)
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从首次给药(第1天)至药代动力学采样结束(第48周)
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AHB-137的最大观察血浆浓度(Cmax)
大体时间:从首次给药(第1天)至药代动力学采样结束(第48周)
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从首次给药(第1天)至药代动力学采样结束(第48周)
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AHB-137的最大观察血浆浓度时间(Tmax)
大体时间:从首次给药(第1天)至药代动力学采样结束(第48周)
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从首次给药(第1天)至药代动力学采样结束(第48周)
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AHB-137的表观血浆清除率(CL/F)
大体时间:从首次给药(第1天)至药代动力学采样结束(第48周)
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从首次给药(第1天)至药代动力学采样结束(第48周)
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Proportion of participants with HBsAg < LOD and HBV DNA < LLOQ
大体时间:Off-treatment follow-up (Week 48 to 72)
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Off-treatment follow-up (Week 48 to 72)
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Proportion of participants with HBsAg < LOD
大体时间:Week 72
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Week 72
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Proportion of participants with HBV DNA < LLOQ
大体时间:From baseline through Week 72
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From baseline through Week 72
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Proportion of participants with protocol-defined virologic response for HBsAg and HBV DNA post AHB-137 treatment
大体时间:24 weeks post AHB-137 treatment
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24 weeks post AHB-137 treatment
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Proportion of participants with protocol-defined virologic response for HBsAg and HBV DNA at weeks 48 and 72
大体时间:24 weeks post AHB-137 treatment and at Week 72
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24 weeks post AHB-137 treatment and at Week 72
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Proportion of participants with protocol-defined virologic response for HBsAg and HBV DNA
大体时间:From baseline through end of study (Week 72)
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From baseline through end of study (Week 72)
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Proportion of participants with HBsAg < or ≥ LOD (0.05 IU/mL) and/or HBV DNA < or ≥ LLOQ
大体时间:From baseline through end of study (Week 72)
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From baseline through end of study (Week 72)
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Proportion of participants with highly sensitive HBsAg < LOD (0.005 IU/mL)
大体时间:From baseline through end of study (Week 72)
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From baseline through end of study (Week 72)
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Proportion of participants with protocol-defined levels of HBsAg
大体时间:From baseline through end of study (Week 72)
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From baseline through end of study (Week 72)
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Categorical change from baseline in 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
大体时间:From baseline through end of study (Week 72)
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From baseline through end of study (Week 72)
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Quantitative hepatitis B virologic and serologic markers over time
大体时间:From baseline through end of study (Week 72)
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Actual values and change from baseline over time in available quantitative hepatitis B surface antigen (HBsAg), hepatitis B surface antibody (HBsAb), hepatitis B virus (HBV) DNA, HBV ribonucleic acid (RNA), hepatitis B core-related antigen (HBcrAg), hepatitis B e antibody (HBeAb), and qualitative and/or quantitative hepatitis B e antigen (HBeAg), summarized descriptively.
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From baseline through end of study (Week 72)
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Time from nucleos(t)ide analog (NA) therapy discontinuation to virologic relapse
大体时间:From NA therapy discontinuation (Week 48) through end of follow-up (Week 72)
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From NA therapy discontinuation (Week 48) through end of follow-up (Week 72)
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Change from baseline in alanine aminotransferase (ALT)
大体时间:From baseline through end of study (Week 72)
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From baseline through end of study (Week 72)
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Proportion of participants with baseline ALT above the upper limit of normal (ULN) who achieve ALT normalization
大体时间:From baseline through end of study (Week 72)
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From baseline through end of study (Week 72)
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Proportion of patients with drug-resistant mutations
大体时间:From baseline through end of study (Week 72)
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From baseline through end of study (Week 72)
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Proportion of participants with treatment-emergent adverse events (TEAEs)
大体时间:From first dose (Day 1) through end of study (Week 72)
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Proportion of participants who experience treatment-emergent adverse events (TEAEs), serious adverse events (SAEs), and adverse events leading to discontinuation of study treatment.
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From first dose (Day 1) through end of study (Week 72)
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Proportion of participants with detectable anti-drug antibody (ADA) to AHB-137 and corresponding ADA titers
大体时间:From baseline through end of study (Week 72)
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From baseline through end of study (Week 72)
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Area Under the Plasma Concentration-Time Curve (AUC) of AHB-137
大体时间:From first dose (Day 1) through end of study (Week 72)
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From first dose (Day 1) through end of study (Week 72)
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Plasma Concentration of AHB-137 at the End of the Dosing Interval (Cτ)
大体时间:From first dose (Day 1) through end of study (Week 72)
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From first dose (Day 1) through end of study (Week 72)
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Maximum Observed Plasma Concentration (Cmax) of AHB-137
大体时间:From first dose (Day 1) through end of study (Week 72)
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From first dose (Day 1) through end of study (Week 72)
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Time to Maximum Observed Plasma Concentration (Tmax) of AHB-137
大体时间:From first dose (Day 1) through end of study (Week 72)
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From first dose (Day 1) through end of study (Week 72)
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Apparent Plasma Clearance (CL/F) of AHB-137
大体时间:From first dose (Day 1) through end of study (Week 72)
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From first dose (Day 1) through end of study (Week 72)
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 研究主任:Audrey Lau, MD, PhD、AusperBio Therapeutics Inc.
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (估计的)
2026年8月27日
初级完成 (估计的)
2027年5月11日
研究完成 (估计的)
2028年7月26日
研究注册日期
首次提交
2026年5月28日
首先提交符合 QC 标准的
2026年6月12日
首次发布 (实际的)
2026年6月17日
研究记录更新
最后更新发布 (实际的)
2026年8月26日
上次提交的符合 QC 标准的更新
2026年8月24日
最后验证
2026年8月1日
更多信息
与本研究相关的术语
关键字
其他相关的 MeSH 术语
其他研究编号
- AB-10-8012
- 2025 (美国 NIH 拨款/合同:Faculty of Social Sciences Scientific Grant at the University of Gdańsk)
- 2025-524159-30-00 (克蒂斯)
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
不
药物和器械信息、研究文件
研究美国 FDA 监管的药品
是的
研究美国 FDA 监管的设备产品
不
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.