Evaluation of Intrahepatic Immune and Virological Response to Tenofovir Alafenamide With Fine Needle Aspiration Biopsy in Chronic Hepatitis B: an Investigator-Initiated, Cohort Study
试验速览
- 阶段
- 4 期
- 入组人数
- 15
- 试验地点
- 1
- 主要终点
- TAF-mediated reduction of inflammatory gene expression in intraheaptic immune cells
研究概览
简要总结
The objective of this study is to identify immunological mechanisms that contribute to normalization of liver inflammation in chronic hepatitis B (CHB) patients starting the antiviral nucleoside analogue, Tenofovir alafenamide (TAF).
详细描述
Investigator-initiated, phase 4 study in which recruited patients will receive, TAF 25mg once daily, for 48 weeks (Figure 1 and Table 1). The total duration of the study to End of Follow-up (EOF) will be 48 weeks. After Week 48, participants will be offered 2 years of TAF therapy. Sample collection 0, 12, 24 w was chosen to analyze immune responses based on ALT normalization rates. This mono-center study will be conducted at Toronto Centre for Liver Disease, Canada.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •• Age >18 years
- •Chronic hepatitis B (HBsAg positive ≥ six months)
- •HBeAg positive or negative
- •ALT >19 for females and >30 for males (AASLD criteria)
- •HBV DNA>4 log IU/mL for HBeAg positive and >3 log for HBeAg negative patients
- •No oral antiviral treatment or IFN for ≥6 months
- •Adequate contraception. For males, at least one method of contraception should be used and for females, a barrier contraception method should be used in combination with one other form of contraception.
- •Written informed consent
排除标准
- •• Treatment with any investigational drug within 60 days of entry into this protocol
- •Immune-suppressive treatment within the previous 6 months
- •History of decompensated cirrhosis (defined as direct (conjugated)
- •bilirubin > 1.2 × ULN,
- •prothrombin time (PT) > 1.2 × ULN
- •platelets < 100,000/mm3
- •serum albumin < 3.5 g/dL
- •prior history of clinical hepatic decompensation (jaundice in the presence of cirrhosis, ascites, gastric bleeding, oesophageal varices or encephalopathy)
- •Liver transplantation
- •Co-infection with hepatitis C virus, hepatitis D virus or HIV
- •Other significant liver disease: alcoholic liver disease, drug-related liver disease, auto-immune hepatitis, hemochromatosis, Wilson's disease or alpha-1 antitrypsin deficiency
- •Estimated glomerular filtration rate <50 mL/min/1.73m2 or any significant renal disease.
- •Alpha-fetoprotein > 50 ng/ml
- •Pregnancy, breast-feeding
- •Other significant medical illness that might interfere with this study: significant pulmonary dysfunction in previous 6 months, malignancy other than skin basocellular carcinoma in previous 5 years, immunodeficiency syndromes (e.g. HIV positivity, auto-immune diseases, organ transplants other than cornea and hair transplant)
- •Substance abuse, such as alcohol (≥80 g/day), I.V. drugs and inhaled drugs in past 2 years. Current methadone usage is allowed.
- •Any other condition which in the opinion of the investigator would make the patient unsuitable for enrolment, or could interfere with the patient participating in and completing the study
研究组 & 干预措施
Tenofovir Alafenamide
Tenofovir Alafenamide 25mg, Dosed orally, once daily with or without food.
干预措施: Tenofovir Alafenamide (Drug)
结局指标
主要结局
TAF-mediated reduction of inflammatory gene expression in intraheaptic immune cells
时间窗: 3 years
Longitudinal samples collected from each patient will be used to measure changes in intrahepatic and peripheral innate and adaptive immune composition, function and gene expression from baseline to ALT normalization after starting TAF.
TAF-mediated reduction of serological markers of HBV replication
时间窗: 3 years
Existing and experimental biomarkers of HBV replication will be measured to compare the viral response to the immune response 1. HBsAg/HBeAg seroclearance 2. HBsAg/HBeAg seroconversion, 3. Serum quantitative HBsAg/HBeAg levels, 4. Serum HBV DNA levels 5. HBV RNA levels 6. Hepatitis B core-related Antigen (HBcrAg) levels; 7. ALT levels.
TAF-mediated reduction of intrahepatic HBV replication intermediates and cccDNA levels
时间窗: 3 years
HBV replication intermediates and cccDNA measured as copies/mg of liver tissue
次要结局
未报告次要终点
研究者
Harry Janssen
Chief of Hepatology | Director Toronto Centre for Liver Disease | Director Viral Hepatitis Care Network (VIRCAN) | Professor of Medicine, University of Toronto |
University Health Network, Toronto