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)
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
注册 (实际的)
阶段
- 阶段2
扩展访问
联系人和位置
学习地点
-
-
-
Ankara、土耳其(türkiye)
- Ankara University Medical School
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
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Males or females, 18 to 65 years of age who are diagnosed with HDV by PCR
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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
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Liver biopsy within the last two years (biopsy can be done at the Screening Visit)
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Positive viral load of >100,000 copies/mL as measured by quantitative PCR
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Electrocardiogram (ECG) shows no acute ischemia or clinically significant abnormality and a QT/QTc interval <450 milliseconds - using Bazett's correction
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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:
- abstinence
- surgical sterilization (bilateral tubal ligation, hysterectomy, bilateral oophorectomy) six months minimum
- IUD in place for at least six months
- barrier methods (condom or diaphragm) with spermicide
- surgical sterilization of the partner (vasectomy for six months)
- hormonal contraceptives for at least three months prior to the first dose of study drug
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Willing and able to comply with study procedures and provide written informed consent
Exclusion Criteria:
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Participation in a clinical trial with or use of any investigational agent within 30 days of Study Visit 1
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Patients co-infected with HIV
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Patients with screening tests positive for HCV, or anti-HIV Ab
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History of decompensated cirrhosis within the past year
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Active jaundice defined by total bilirubin > 2.0 excluding Gilbert's disease
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INR ≥ 1.5
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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)
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Drug abuse within the last six months with the exception of cannabinoids and their derivatives
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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)
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History or clinical evidence of any of the following:
- variceal bleeding, ascites, hepatic encephalopathy, CTP score > 6, decompensated liver disease or any other form of non-viral hepatitis
- 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)
- any malignancy within 3 years except for basal cell skin cancer
- significant or unstable cardiac disease (e.g., angina, congestive heart failure, uncontrolled hypertension, history of arrhythmia)
- chronic pulmonary disease (e.g., chronic obstructive pulmonary disease) associated with functional impairment
- severe or uncontrolled psychiatric disease, including severe depression, history of suicidal ideation, suicidal attempts or psychosis requiring medication and/or hospitalization 2
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Patients with a body mass index > 30 kg/m^2
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Concomitant drugs known to prolong the QT interval
学习计划
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:
CYP 3A4 inhibitor, lonafarnib booster
其他名称:
|
|
实验性的:lonafarnib/ritonavir - II
lonafarnib 100 mg BID + ritonavir 50 mg BID |
antiviral farnesyl transferase inhibitor
其他名称:
CYP 3A4 inhibitor, lonafarnib booster
其他名称:
|
|
实验性的:lonafarnib/ritonavir - III
lonafarnib 100 mg QD + ritonavir 100 mg QD |
antiviral farnesyl transferase inhibitor
其他名称:
CYP 3A4 inhibitor, lonafarnib booster
其他名称:
|
|
实验性的:lonafarnib/ritonavir - IV
lonafarnib 150 mg QD + ritonavir 100 mg QD |
antiviral farnesyl transferase inhibitor
其他名称:
CYP 3A4 inhibitor, lonafarnib booster
其他名称:
|
|
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:
CYP 3A4 inhibitor, lonafarnib booster
其他名称:
immunomodulator
其他名称:
|
|
实验性的:lonafarnib/ritonavir - VI
lonafarnib 25 mg BID + ritonavir 100 mg BID |
antiviral farnesyl transferase inhibitor
其他名称:
CYP 3A4 inhibitor, lonafarnib booster
其他名称:
|
|
实验性的:lonafarnib/ritonavir - VII
lonafarnib 50 mg BID + ritonavir 100 mg BID |
antiviral farnesyl transferase inhibitor
其他名称:
CYP 3A4 inhibitor, lonafarnib booster
其他名称:
|
|
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:
CYP 3A4 inhibitor, lonafarnib booster
其他名称:
immunomodulator
其他名称:
|
|
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:
CYP 3A4 inhibitor, lonafarnib booster
其他名称:
immunomodulator
其他名称:
|
|
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:
CYP 3A4 inhibitor, lonafarnib booster
其他名称:
immunomodulator
其他名称:
|
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
出版物和有用的链接
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- EIG-300-Amendment 3
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
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