Liver Biopsy Following Gene Therapy For Hemophilia
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 8
- 试验地点
- 1
- 主要终点
- Assessment of the number of hepatocytes transduced with AAV vector genome in liver biopsy samples analyzed by FISH
研究概览
简要总结
This observational study will obtain liver biopsy samples and evaluate the long-term effect of adeno-associated virus (AAV)-mediated gene therapy on the liver tissue in adult patients with hemophilia A or hemophilia B who have previously been treated with a factor VIII or factor IX gene-containing AAV-vector for liver-targeted gene transfer. Participants are from a cohort of patients treated with AAV-mediated gene transfer and at least 6 months after vector infusion.
详细描述
This is a prospective cohort study evaluating the effect of AAV-mediated gene therapy on the liver in adult patients with hemophilia A or hemophilia B who have previously been treated with a FVIII/FIX gene-containing AAV-vector for liver-targeted gene transfer.
To better understand the effect of AAV-mediated gene transfer on the liver, eligible participants can allow the use and analysis of already existing liver tissue samples, taken and preserved after having received gene therapy. Alternatively, eligible participants can consent to providing a new liver tissue sample which will be obtained by undergoing a standard transjugular liver biopsy (TJLB) procedure under moderate sedation. . The procedure will be done as outpatient (day 1) with post procedure follow-up on day 2, 3, 4 and 14.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 80 Years（Adult, Older Adult）
- 性别
- Male
- 接受健康志愿者
- 否
入选标准
- •Age ≥18 to 80 years
- •Patients, who were enrolled and treated in one of the following clinical trials:
- •AGT4HB (EudraCT number: 2005-005711-17; NCT00979238) - FIX AAV gene therapy trial (sponsor: St. Jude Children's Research Hospital)
- •GO8 (EudraCT number:2014-003880-38; NCT02576795) - FVIII AAV gene therapy trial (sponsor: University College, London)
- •Able to give informed consent
- •Able to comply with study requirements
排除标准
- •(Do not apply to participants who will not undergo liver biopsy, and have leftover liver tissue from a previous biopsy procedure, because all exclusion criteria only cover the safety considerations for the biopsy procedure.):
- •Any condition that, in the opinion of the investigator or sponsor of the ongoing clinical trial in which the patient is participating in, would prevent the patient from fully complying with the requirements of the clinical trial and/or would influence or interfere with evaluation and interpretation of subject safety or efficacy result of that ongoing clinical trial
- •Platelet count <140x10^9/L
- •INR >1.5
- •Abnormal kidney function with estimated GFR <50 mL/min (calculated using the CKD-EPI equation)
- •Known allergy to iodine-based intravenous contrast agents
- •Known allergy to local or general anesthetics
- •Known allergic reaction to FVIII/FIX concentrate infusions
- •Presence of FVIII inhibitor or FIX inhibitor (historical result can be used if done within 14 weeks of this liver biopsy)
- •Evidence of any bleeding disorder other than hemophilia A or B
研究组 & 干预措施
Participants
Those who meet the Eligibility Criteria
干预措施: Liver Biopsy (Procedure)
结局指标
主要结局
Assessment of the number of hepatocytes transduced with AAV vector genome in liver biopsy samples analyzed by FISH
时间窗: single time point (day of biopsy)
Fluorescence in situ hybridization (FISH)
次要结局
- The degree of hepatocyte damage at a morphological level(single time point (day of biopsy))
- The number of hepatocytes revealing FVIII/FIX RNA in-situ transcripts(single time point (day of biopsy))
- The number and types of epigenetic changes within the AAV genome in the liver(single time point (day of biopsy))
- The qualitative and quantitative assessment of the RNA transcriptome(single time point (day of biopsy))
- The number and type of hot spots for integration of AAV provirus in liver cells(single time point (day of biopsy))