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Safety and Effectiveness of Short-Term Anti-HIV Drug Therapy for Recent HIV-1 Infection

2013年1月16日 更新者:University of Colorado, Denver

An Open-Label Randomized Clinical Trial to Evaluate the Efficacy and Safety of Short Course Antiretroviral Therapy for Acute or Recent HIV-1 Infection in Zimbabwe and the United States

The purpose of this study is to determine the safety and effectiveness of an anti-HIV drug regimen followed by treatment interruption in people recently infected with HIV. This study will also compare the effects of a treatment regimen including treatment interruption with a treatment plan based on clinical indicators.

研究概览

详细说明

About 6 months after infection, HIV viral load reaches a temporarily stable level known as virus set point. Virus set point is different for each patient and can be a predictor for disease progression. Preliminary studies indicate that early, short-term antiretroviral therapy (ART) given to people newly infected with HIV may lead to lower virus set points and preserved CD4 counts. However, the length of short-term treatment needed to balance the possible adverse effects of ART with the achievement of lower virus set point is not yet known. By lowering the virus set point and maintaining CD4 counts, the need for long-term ART may be postponed. The purpose of this study is to determine the safety and efficacy of a short course of ART on producing a lower virus set point in adults recently infected with HIV.

This study will last at least 28 weeks. Participants will be randomly assigned to one of two arms. Arm A will receive ART for 12 weeks as emtricitabine/tenofovir disoproxil fumarate (TDF/FTC) daily and lopinavir/ritonavir (LPV/RTV) in tablet form twice daily. After 12 weeks, treatment will be interrupted unless the CD4 count is measured to be less than 350 cells/mm^3 on two consecutive occasions during treatment interruption. If that occurs therapy will be resumed. Participants in Arm B will receive no treatment until cluster of differentiation 4 (CD4) counts drop below 350 cells/mm^3, indicating ART is needed. Study visits will occur at study entry, at Weeks 2 and 4, and every 4 weeks thereafter. At each study visit, a physical exam, blood collection, and completion of an adherence questionnaire will occur. Participants are encouraged to enroll in a related substudy that will evaluate HIV viral load in genital secretions.

研究类型

介入性

注册 (实际的)

16

阶段

  • 不适用

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

      • Harare、津巴布韦
        • University of Zimbabwe College of Health Sciences
    • Colorado
      • Denver、Colorado、美国、80262
        • University of Colorado Health Sciences Center
    • Georgia
      • Atlanta、Georgia、美国、30308
        • AIDS Research Consortium of Atlanta

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 及以上 (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:

  • Acute or recent HIV-1 infection. More information about this criterion can be found in the protocol.
  • CD4 count 500 cells/mm3 or greater
  • No evidence of prior or current AIDS-defining illness
  • No signs or symptoms of HIV infection or AIDS-defining illness that, in the opinion of the investigator, requires ART
  • Willing to use acceptable forms of contraception

Exclusion Criteria:

  • Prior treatment with any antiretroviral drug for more than 7 days
  • Use of certain drugs within 21 days of study entry
  • Prior receipt of investigational anti-HIV-1 vaccine
  • Ongoing therapy with systemic corticosteroids, chemotherapeutic agents, nephrotoxic systemic agents, immunomodulatory treatments, or investigational agents
  • Known allergy/sensitivity to study drugs or their formulations
  • Current drug or alcohol use or abuse that, in the opinion of the investigator, may interfere with the study
  • Serious medical or psychiatric illness that may interfere with the study
  • Hepatitis B infected
  • Pregnancy or breastfeeding

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:Treatment interruption
Oral Tenofovir disoproxil fumarate/Emtricitabine and Lopinavir/Ritonavir for 12 weeks followed by treatment interruption if CD4 count is 450 mm^3 or higher. When CD4 count is less than 350 mm^3 on two separate, consecutive measurements during treatment interruption, therapy will be resumed.
300 mg Tenofovir disoproxil fumarate/ 200 mg emtricitabine tablet taken orally once daily
其他名称:
  • TDF/FTC
Three 400 mg lopinavir/ 100 mg ritonavir soft gel capsules taken orally twice daily
其他名称:
  • LPV/RTV
实验性的:CD4 T cell guided therapy
Anti Retroviral Therapy initiated when AIDS-defining illness occurs or if CD4 count is confirmed at less than 350 mm^3 at two separate, consecutive measurements
300 mg Tenofovir disoproxil fumarate/ 200 mg emtricitabine tablet taken orally once daily
其他名称:
  • TDF/FTC
Three 400 mg lopinavir/ 100 mg ritonavir soft gel capsules taken orally twice daily
其他名称:
  • LPV/RTV

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
Plasma HIV-1 Viral Load (Copies/ml) at Week 24 as Compared Between the Two Arms
大体时间:At Week 24
At Week 24
Number of Participants Experiencing Either an AIDS-defining Event, a Grade 3 or 4 Adverse Event, or Acute Retroviral Syndrome
大体时间:At Week 24
At Week 24
Viral Set Point
大体时间:Throughout study
set point is reached after the immune system has developed HIV antibodies and begins to attempt to fight the virus
Throughout study

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。

调查人员

  • 学习椅:Michelle A. Barron, MD、Division of Infectious Disease, University of Colorado Health Sciences Center
  • 学习椅:Margaret Borok, MRCP、Department of Medicine, University of Zimbabwe

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

2007年1月1日

初级完成 (实际的)

2010年2月1日

研究完成 (实际的)

2010年2月1日

研究注册日期

首次提交

2006年12月19日

首先提交符合 QC 标准的

2006年12月19日

首次发布 (估计)

2006年12月21日

研究记录更新

最后更新发布 (估计)

2013年2月20日

上次提交的符合 QC 标准的更新

2013年1月16日

最后验证

2013年1月1日

更多信息

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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