The Immunologic Effects of HCV Therapy With Fixed Dose Combination Ledipasvir/Sofosbuvir (HARVONI) in HCV Genotype 1 Chronically Mono-infected Active and Former IDUs.
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 34
- 试验地点
- 1
- 主要终点
- sCD14 (ng/mL)
研究概览
简要总结
The investigator's hypothesis is that active injectors will show a partial reduction in markers of immune activation with HCV therapy whereas non-injectors will show a more significant reduction in these markers, and will exhibit levels of immune activation that approach that seen in similarly studied healthy volunteers.This is based on observations that this group of investigators have made. They have shown that individuals who inject drugs have high level of immune activation in blood and tissue. Immune activation or chronic inflammation has been associated with accelerated aging, cardiovascular, renal and liver disease as well as CNS dysfunction. It remains unclear whether increased levels of immune activation are due to non-sterile injection of drugs, chronic infection with Hepatitis C, chronic opiate use, or perhaps combinations of all 3. To understand the potential contribution of infection with Hepatitis C the investigators will compare levels of immune activation pre- and post treatment with an all oral, one pill once daily, interferon sparing treatment of HCV in 2 groups of chronically HCV infected patients- one actively injecting with drugs and the other free of injection for at least 4 months. Immune activation comparisons will also include non-injecting healthy volunteers.
详细描述
This group of multidisciplinary investigators has discovered increased levels of immune activation among HIV-1-uninfected active injection drug users (IDUs) when compared to non-IDU controls . The vast majority (80%) are also infected with HCV.
Active injectors have high levels of immune activation as measured by sCD14, CD8 co-expression of CD38 and HLA-DR, as well as Type 1 cytokines.
Within months of ceasing injecting, there are observable decreases in some parameters however in general they remain elevated when compared to non-injecting healthy volunteers.
As approximately 80% of these subjects are HCV infected and viremic, these results are confounded as to the cause of the observed increased levels of markers of immune activation- active injection or chronic Hepatitis C. Until recently HCV treatment required the use of IFN which has immunomodulatory activity which would cause perturbations in the markers of immune activation. However the development of direct acting agents (DAA) to treat HCV has revolutionized therapy. In this trial the investigators will employ the once daily FDC formulation of sofosbuvir and ledipasvir to assess changes in markers of immune activation during therapy.
There have been multiple clinical trials of FDC LDV-SOF in patients with Genotype 1 HCV. When taken once daily for 12 weeks, sustained virologic response rates have been very high with response rates nearing 99% in most studies with a 12-week course of therapy.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 55 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Ability to give written informed consent in English
- •Age≥18 and ≤55
- •HCV antibody positive
- •HCV RNA >1,000 copies/mL plasma
- •HCV treatment naive
- •HCV genotype 1a or 1b or mixed type 1
- •AST, ALT <10x ULN
- •Direct bilirubin <3.0
- •Platelet count >50,000
- •Creatinine clearance >30mL/min as estimated by Cockroft Gault
- •Hemoglobin >10 if female, >11 if male
- •Albumin > 2.8
- •If Group A: urine dip for opiates + and active injection drug use of heroin defined as injecting at least 3 times per week.
- •If Group B then no IDU for at least 4 months and a negative urine for opiates at screening.
- •Venous access for phlebotomy
- •Willingness to agree to effective contraception during the course of the study.
- •If Group C: - negative urine for opiates at screening
- •no recreational drug use for at least 2 years (excluding marijuana)
- •HIV, HCV and HBV uninfected
排除标准
- •HIV infection
- •Chronic infection with Hepatitis B
- •Uncompensated cirrhosis
- •Required use of:
- •Anticonvulsants: carbamazepine, oxycarbazepine, phenobarbital, and phenytoin
- •Antimycobacterials: rifabutin, rifampin, rifapentine
- •Herbal Supplements: St. John's wort
- •HIV Protease Inhibitors: tipranavir-ritonavir
- •Antiarrhythmic Drugs: amiodarone (Cordarone, Nexterone, Pacerone)
- •Any medical condition that in the opinion of the investigator would interfere with study participation and medical adherence
- •Pregnancy/breast feeding
研究组 & 干预措施
Former injection drug use (former IDU)
In former IDU, Harvoni (Fixed dose combination ledipasvir/sofosbuvir), one pill orally daily x 12 weeks
干预措施: Harvoni (Fixed dose combination ledipasvir/sofosbuvir) (Drug)
Active injection drug use (IDU)
In active IDU, Harvoni (Fixed dose combination ledipasvir/sofosbuvir), one pill orally daily x 12 weeks
干预措施: Harvoni (Fixed dose combination ledipasvir/sofosbuvir) (Drug)
结局指标
主要结局
sCD14 (ng/mL)
时间窗: 24 weeks
Marker of immune activation as measured by levels of soluble CD14. Note that the levels of sCD14 were only measured at baseline in the Healthy Volunteers group and therefore there are no data for weeks 4, 12, or 24 entered.
次要结局
- Virologic Response to Therapy as Measured by HCV RNA(24 weeks)
- Gene Expression Profiles(24 weeks)
研究者
Martin Markowitz
Aaron Diamond Professor/Clinical Director
Rockefeller University