IL-15 脉冲给药耗尽 HIV 感染者体内储库的原理研究证明 (ALT-803)
IL-15 脉冲给药耗尽 HIV 感染者储库的原理证明优化 ART 检测不到血浆 HIV RNA
To assess the safety and tolerability of ALT-803, as well as, the potential efficacy of ALT-803 in HIV
研究概览
详细说明
This is an open-label, single-arm intra-patient dose escalating pilot study of ALT-803, a recombinant human super agonist interleukin-15 (IL-15) complex with an expansion cohort at the maximum tolerated dose (MTD). The primary aim is to investigate the safety and tolerability of ALT-803 in HIV-infected people receiving potent and optimized antiretroviral therapy. All infusions will occur on a Monday. Subjects will be monitored for 24 hours after the first infusion and then for 6 hours after each subsequent infusion, provided no unacceptable toxicity.
研究类型
注册 (实际的)
阶段
- 阶段1
联系人和位置
学习地点
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Minnesota
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Minneapolis、Minnesota、美国、55455
- University of Minnesota
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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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HIV-1 infected adults aged 18 years or over.
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Stable ART for at least 36 months
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Screening plasma HIV RNA levels below level of quantification (<40 to <50 copies RNA/mL depending on the assay) ≥ 2 years (a single measurement above the level of detection but < 100-200 copies/ml will be allowed)
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Screening CD4 count ≥500 cells/mm3
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Laboratory tests performed within 14 days of study enrollment:
- WBC ≥ 3000/mm3
- Platelets ≥ 50,000/mm3 [Patients may be transfused to meet this requirement]
- Hemoglobin ≥ 8 g/dL (>80g/L) [Patients may be transfused to meet this requirement]
- Calculated glomerular filtration rate (GFR) >45 mL/min/1.73m2
- Total bilirubin ≤ 2.0 X upper limit of institutional normal (ULN)
- AST, ALT, ALP ≤ 2.0 X ULN
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Adequate pulmonary function without any clinical sign of severe pulmonary dysfunction. PFTs > 50% of predicted if symptomatic or prior known impairment.
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Ability to be off prednisone and other immunosuppressive drugs for at least 14 days before first dose of study drug
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Women of child bearing potential and men with partners of child bearing potential must agree to use effective contraception during therapy and for 4 months after completion of therapy
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Voluntary written consent
Exclusion Criteria:
- Active infection other than HIV currently requiring systemic antimicrobial therapy
- Previously treated on this study or received previous ALT-803
- Latent TB infection or active TB disease prior to completing a standard regimen of anti-TB therapy
- Active fungal infection requiring systemic antifungal therapy
- Active or recurrent herpes or varicella-zoster virus infection requiring treatment (or chronic suppression)
- Chronic hepatitis B or C
- Planning or current pregnancy or breastfeeding
- Intended modification of antiretroviral therapy in the next 24 weeks
- NYHA (New York Heart Association) Class III or IV heart failure, uncontrollable supraventricular arrhythmias, any history of a ventricular arrhythmia, or other clinical signs of severe cardiac dysfunction
- Symptomatic congestive heart failure, unstable angina pectoris, or Myocardial infarction within 6 months prior to screening
- Marked baseline prolongation of QT/QTc interval (e.g. demonstration of a QTc interval greater than 500 milliseconds)
- History or evidence of uncontrollable CNS disease
- Prior organ allograft or allogeneic transplantation
- On-going chronic systemic or regular inhaled corticosteroid use or other immunosuppressive therapy (a history of mild asthma not requiring therapy is eligible)
- Psychiatric illness/social situations that would limit compliance with study requirements
- Other illness that in the opinion of the investigator would exclude the patient from participating in this study
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:不适用
- 介入模型:单组作业
- 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:ALT-803
ALT-803 |
Interleukin 15 (IL-15) is a common γ-chain cytokine that is related to interleukin-2 (IL-2) and is a critical factor for the development, proliferation, and activation of effector natural killer (NK) and CD8+ memory T cells |
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 |
|---|---|---|
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Assess the safety and tolerability of ALT-803 in HIV-infected subjects
大体时间:4 weeks
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Safety and tolerability is determined by the incidence of adverse events, size of the inducible reservoir as estimated using the TILDA assay |
4 weeks
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Assess the impact of ALT-803 on the size of the inducible reservoir,
大体时间:4 weeks
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Assess the impact of ALT-803 on the size of the inducible reservoir, as estimated using the TILDA assay, in total CD4+ T cells and memory subsets |
4 weeks
|
合作者和调查者
调查人员
- 首席研究员:Tim Schacker, MD、University of Minnesota
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
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