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在 HDV (LOWR-2) 中,Lonafarnib 与利托那韦结合使用和不使用聚乙二醇干扰素 Alfa-2a (PEG IFN-a) (LOWR-2)

2026年9月3日 更新者:EIT Pharma, Inc.

一项开放标签、剂量范围、概念验证研究,以评估 Lonafarnib 与利托那韦增强 +/-聚乙二醇干扰素 Alfa-2a 在慢性感染三角洲肝炎 (HDV) (LOWR-2) 患者中的安全性和有效性

An Open-label, Dose-ranging Study to Evaluate the Safety and Efficacy of Lonafarnib with Ritonavir Boosting +/- Peginterferon alfa-2a in Patients Chronically Infected with Delta Hepatitis (HDV) (LOWR-2).

研究概览

详细说明

Chronic delta hepatitis is a serious form of chronic liver disease caused by infection with the hepatitis D virus (HDV), a small RNA virus that requires farnesylation of its major structural protein (HDV antigen) for replication. Up to sixty subjects with chronic delta hepatitis will be randomized to receive one of ten different doses of lonafarnib. Dosing will occur over 12-48 weeks, and during that time, evidence of antiviral response will be assessed by frequent measurements of HDV-RNA. The primary therapeutic endpoint will be an improvement in quantitative serum HDV RNA levels after treatment with lonafarnib therapy. The primary safety endpoint will be the ability to tolerate the drug at the prescribed dose for the treatment duration. Several secondary endpoints will be measured, including side effects, ALT levels, and symptoms. Therapy will be stopped for intolerance to lonafarnib. This study is designed as a Phase 2a study assessing the safety, tolerance and antiviral activity of nine dosing combinations of lonafarnib with ritonavir boosting with and without peginterferon alfa-2a (PEG IFN-a).

研究类型

介入性

注册 (实际的)

55

阶段

  • 阶段2

扩展访问

得到正式认可的 出售给公众。 查看扩展访问记录。

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。

学习地点

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

18年 至 65年 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Males or females, 18 to 65 years of age who are diagnosed with HDV by PCR

  • Chronic hepatitis D infection, genotype 1, documented by a positive anti-HDV Ab test at least of 6 months duration and detectable HDV RNA by PCR within 3 months to study entry

  • Liver biopsy within the last two years (biopsy can be done at the Screening Visit)

  • Positive viral load of >100,000 copies/mL as measured by quantitative PCR

  • Electrocardiogram (ECG) shows no acute ischemia or clinically significant abnormality and a QT/QTc interval <450 milliseconds - using Bazett's correction

  • Females of childbearing potential (intact uterus and within 1 year since the last menstrual period) should be non-lactating and have a negative serum pregnancy test. In addition, these subjects should agree to use one of the following acceptable birth control methods throughout the study:

    1. abstinence
    2. surgical sterilization (bilateral tubal ligation, hysterectomy, bilateral oophorectomy) six months minimum
    3. IUD in place for at least six months
    4. barrier methods (condom or diaphragm) with spermicide
    5. surgical sterilization of the partner (vasectomy for six months)
    6. hormonal contraceptives for at least three months prior to the first dose of study drug
  • Willing and able to comply with study procedures and provide written informed consent

Exclusion Criteria:

  • Participation in a clinical trial with or use of any investigational agent within 30 days of Study Visit 1

  • Patients co-infected with HIV

  • Patients with screening tests positive for HCV, or anti-HIV Ab

  • History of decompensated cirrhosis within the past year

  • Active jaundice defined by total bilirubin > 2.0 excluding Gilbert's disease

  • INR ≥ 1.5

  • Eating disorder or alcohol abuse within the past 2 years, excessive alcohol intake (> 20 g per day for females (1.5 standard alcohol drinks) or > 30 g per day for males (2.0 standard alcohol drinks) (a standard drink contains 14 g of alcohol: 12 oz of beer, 5 oz of wine or 1.5 oz of spirits) (1.0 fluid oz (US) = 29.57 mL)

  • Drug abuse within the last six months with the exception of cannabinoids and their derivatives

  • Patients with absolute neutrophil count (ANC) < 1500 cells/mm^3; platelet count < 100,000 cells/mm^3; hemoglobin < 12 g/dL for women and < 13 g/dL for men; abnormal TSH,T4, or T3 or thyroid function not adequately controlled; or serum creatinine concentration ≥ 1.5 times upper limit of normal (ULN)

  • History or clinical evidence of any of the following:

    1. variceal bleeding, ascites, hepatic encephalopathy, CTP score > 6, decompensated liver disease or any other form of non-viral hepatitis
    2. immunologically mediated disease (e.g., rheumatoid arthritis, inflammatory bowel disease, severe psoriasis, systemic lupus erythematosus) requiring more than intermittent nonsteroidal anti-inflammatory medications for management or that requires frequent or prolonged use of corticosteroids (inhaled asthma medications are allowed)
    3. any malignancy within 3 years except for basal cell skin cancer
    4. significant or unstable cardiac disease (e.g., angina, congestive heart failure, uncontrolled hypertension, history of arrhythmia)
    5. chronic pulmonary disease (e.g., chronic obstructive pulmonary disease) associated with functional impairment
    6. severe or uncontrolled psychiatric disease, including severe depression, history of suicidal ideation, suicidal attempts or psychosis requiring medication and/or hospitalization 2
  • Patients with a body mass index > 30 kg/m^2

  • Concomitant drugs known to prolong the QT interval

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
实验性的:lonafarnib/ritonavir - I

lonafarnib 100 mg BID + ritonavir 100 mg QD

antiviral farnesyl transferase inhibitor

其他名称:
  • 萨拉萨尔,EBP994,LNF

CYP 3A4 inhibitor, lonafarnib booster

其他名称:
  • 诺维尔,RTV
实验性的:lonafarnib/ritonavir - II

lonafarnib 100 mg BID + ritonavir 50 mg BID

antiviral farnesyl transferase inhibitor

其他名称:
  • 萨拉萨尔,EBP994,LNF

CYP 3A4 inhibitor, lonafarnib booster

其他名称:
  • 诺维尔,RTV
实验性的:lonafarnib/ritonavir - III

lonafarnib 100 mg QD + ritonavir 100 mg QD

antiviral farnesyl transferase inhibitor

其他名称:
  • 萨拉萨尔,EBP994,LNF

CYP 3A4 inhibitor, lonafarnib booster

其他名称:
  • 诺维尔,RTV
实验性的:lonafarnib/ritonavir - IV

lonafarnib 150 mg QD + ritonavir 100 mg QD

antiviral farnesyl transferase inhibitor

其他名称:
  • 萨拉萨尔,EBP994,LNF

CYP 3A4 inhibitor, lonafarnib booster

其他名称:
  • 诺维尔,RTV
实验性的:lonafarnib/ritonavir/PEG IFN-a - V

lonafarnib 75 mg BID + ritonavir 100 mg BID (+ PEG IFN-a 180 ug QW on Week 12)

antiviral farnesyl transferase inhibitor

其他名称:
  • 萨拉萨尔,EBP994,LNF

CYP 3A4 inhibitor, lonafarnib booster

其他名称:
  • 诺维尔,RTV

immunomodulator

其他名称:
  • 飞马座
  • PEG干扰素-a
  • 聚乙二醇干扰素α-2a
  • PEG IFN-alfa-2a
实验性的:lonafarnib/ritonavir - VI

lonafarnib 25 mg BID + ritonavir 100 mg BID

antiviral farnesyl transferase inhibitor

其他名称:
  • 萨拉萨尔,EBP994,LNF

CYP 3A4 inhibitor, lonafarnib booster

其他名称:
  • 诺维尔,RTV
实验性的:lonafarnib/ritonavir - VII

lonafarnib 50 mg BID + ritonavir 100 mg BID

antiviral farnesyl transferase inhibitor

其他名称:
  • 萨拉萨尔,EBP994,LNF

CYP 3A4 inhibitor, lonafarnib booster

其他名称:
  • 诺维尔,RTV
实验性的:lonafarnib/ritonavir/PEG IFN-a - VIII

lonafarnib 50 mg BID + ritonavir 100 mg BID (+ PEG IFN-a 180 ug QW on Week 12)

antiviral farnesyl transferase inhibitor

其他名称:
  • 萨拉萨尔,EBP994,LNF

CYP 3A4 inhibitor, lonafarnib booster

其他名称:
  • 诺维尔,RTV

immunomodulator

其他名称:
  • 飞马座
  • PEG干扰素-a
  • 聚乙二醇干扰素α-2a
  • PEG IFN-alfa-2a
实验性的:lonafarnib/ritonavir/PEG IFN-a - IX

lonafarnib 25 mg BID + ritonavir 100 mg BID + PEG IFN-a 180 ug QW

antiviral farnesyl transferase inhibitor

其他名称:
  • 萨拉萨尔,EBP994,LNF

CYP 3A4 inhibitor, lonafarnib booster

其他名称:
  • 诺维尔,RTV

immunomodulator

其他名称:
  • 飞马座
  • PEG干扰素-a
  • 聚乙二醇干扰素α-2a
  • PEG IFN-alfa-2a
实验性的:lonafarnib/ritonavir/PEG IFN-a - X

lonafarnib 50 mg BID + ritonavir 100 mg BID + PEG IFN-a 180 ug QW

antiviral farnesyl transferase inhibitor

其他名称:
  • 萨拉萨尔,EBP994,LNF

CYP 3A4 inhibitor, lonafarnib booster

其他名称:
  • 诺维尔,RTV

immunomodulator

其他名称:
  • 飞马座
  • PEG干扰素-a
  • 聚乙二醇干扰素α-2a
  • PEG IFN-alfa-2a

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
≥2 log10 Decline of HDV RNA From Baseline at End of Treatment (EOT)
大体时间:12-48 weeks

Proportion of intent to treat patients with ≥2 log10 decline of HDV RNA from baseline at end of treatment (EOT)

12-48 weeks

次要结果测量

结果测量
措施说明
大体时间
< LLOQ in HDV RNA at End of Treatment (EOT)
大体时间:12-48 weeks

Proportion of intent to treat patients with HDV RNA below the limit of quantitation at end of treatment

12-48 weeks
ALT Normalization at End of Treatment
大体时间:12-48 weeks

Proportion of intent to treat population who normalize ALT at end of treatment

12-48 weeks

其他结果措施

结果测量
措施说明
大体时间
Mean HDV RNA Decline
大体时间:12-48 weeks

mean HDV RNA decline of intent to treat population from baseline to end of treatment

12-48 weeks

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。

合作者

调查人员

  • 首席研究员:Cihan Yurdaydin, MD、Ankara University

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

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 (实际的)

2014年12月1日

初级完成 (实际的)

2017年4月18日

研究完成 (实际的)

2017年6月15日

研究注册日期

首次提交

2015年4月21日

首先提交符合 QC 标准的

2015年4月25日

首次发布 (估计的)

2015年4月30日

研究记录更新

最后更新发布 (实际的)

2026年9月25日

上次提交的符合 QC 标准的更新

2026年9月3日

最后验证

2023年3月1日

更多信息

与本研究相关的术语

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.

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