A Pilot Study to Assess the Safety and Effect on HIV Transcription of Vorinostat in Patients Receiving Suppressive Combination Anti-retroviral Therapy
试验速览
- 阶段
- 2 期
- 发起方
- 入组人数
- 20
- 试验地点
- 1
- 主要终点
- To evaluate the effect of vorinostat on HIV transcription in CD4 T-cells.
研究概览
简要总结
The objective of the study is to assess the safety and ability of vorinostat, a drug currently licensed for the treatment of a type of lymphoma, to 'turn on' dormant HIV infected CD4 T-cells.
详细描述
Treatment of HIV infection with combination antiretroviral therapy (cART) has led to significant improvements in the life expectancy and quality of life of people living with HIV. Nevertheless, life expectancy is significantly lower than uninfected individuals and cART leads to several long term side effects. cART alone is not able to cure HIV infection due to persistence of HIV infection in dormant cells. One potential strategy to eradicate HIV infection is to 'wake up' these dormant infected cells by 'turning on' the cell. The small number of cells that are dormant and infected would start to produce virus and die, but infection of other cells would be prevented by cART. Ultimately this could lead to eradication of dormant infected cells and a potential cure for HIV.
This study is a pilot study in 20 individuals recruited at the Alfred Hospital only.
The hypotheses is that vorinostat will induce HIV transcription in CD4 T-cells with latent HIV infection, it is safe and well tolerated in patients receiving effective cART and will induce histone acetylation in vivo in patients with HIV infection.
The study will run over 12 weeks, involving 9 study visits for the participant. Eligible patients must be between 18 to 60 years of age with confirmed HIV infection, and receiving successful cART as indicated by 'suppressed' HIV virus in blood (plasma HIV RNA <50 copies/ml) for at least 3 years and a strong immune system (two CD4 counts greater than 500 cell/µl in the last 6 months).
Patients will be reviewed at screening and days 1 (three time points), 2, 7, 14, 21, 28 and 84 (week 12). They will have blood tests for HIV viral load assessment, CD4 cell counts, biochemistry, hematology and storage samples. An electrocardiogram of the heart (ECG) will be taken at screening, day 7 and 14.
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 60 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •HIV -1 infected adults
- •HIV-1 plasma RNA <50 copies/ml for at least 3 years with at least 2 viral load measures per year, and most recent viral load within 3 months of screening. Episodes of a single HIV plasma RNA 50-199 copies/ml will not exclude participation if the subsequent HIV plasma RNA was <50 copies/ml.
- •Receiving combination antiretroviral therapy (at least 3 agents)
- •In the last 6 months have two CD4 cell count greater than 500 cell/µl
- •Documented subtype B HIV infection
- •Detectable HIV RNA on stored specimen
- •Able to give informed consent
排除标准
- •Any significant acute medical illness in the past 8 weeks.
- •Any evidence of an active AIDS-defining opportunistic infection.
- •Current or recent gastrointestinal disease that may impact the absorption of study drug.
- •Any gastrointestinal surgery that could impact upon the absorption of study drug.
- •Active alcohol or substance use that, in the Investigator's opinion, will prevent adequate compliance with study therapy .
- •Moderate to severe hepatic impairment
- •Hepatic transaminases (AST or ALT) > 3 x upper limit of normal (ULN)
- •Hepatitis B infection as indicated by the presence of Hepatitis B surface antigen or detectable DNA levels in blood.
- •A personal history of clinically significant cardiac disease, symptomatic or asymptomatic arrhythmias, syncopal episodes, or additional risk factors for torsades de pointes (e.g. heart failure).
- •History of malignancy or transplantation, including skin cancers or Kaposi sarcoma
- •History of diabetes mellitus
- •Use of an HIV protease inhibitor.
- •Receipt of immunomodulating agents, immunization or systemic chemotherapeutic agents within 28 days prior to screening.
- •Use of an agent definitely or possibly associated with effects on QT intervals within 2 weeks of screening.
- •Receipt of sodium valproate or other HDAC inhibitor at any time.
- •Women who are pregnant or breastfeeding, or with a positive pregnancy test during screening or Women of Child Bearing Potential (WOCBP) who are unwilling or unable to use an acceptable method of contraception to avoid pregnancy for the entire study period and for at least 4 weeks before and 4 weeks after the study.
- •Males who are unwilling or unable to use barrier contraception during vaginal intercourse from the time of enrollment and for 12 weeks after participation in the study are also excluded.
研究组 & 干预措施
Vorinostat
Vorinostat 400mg ( 4 X 100mg ) orally daily for 14 days
干预措施: Vorinostat (Drug)
结局指标
主要结局
To evaluate the effect of vorinostat on HIV transcription in CD4 T-cells.
时间窗: Day 1 (before drug, 2 and 8 hours after first dose), Day 2, 7, 14, 21 and 28
The primary (efficacy) endpoint of this study is to evaluate the effect of vorinostat on HIV transcription from latently infected CD4+ T-cells as measured by HIV unspliced RNA in CD4+ T-cells.
次要结局
- 1. To evaluate the safety and tolerability of vorinostat in patients receiving effective combination antiretroviral therapy (cART(Screening, Day 1, 7, 14,21, and 28)