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临床试验/NCT04359186
NCT04359186
招募中
不适用

Analytic Treatment Interruption in HIV Infection

University of California, San Francisco1 个研究点 分布在 1 个国家目标入组 40 人2020年10月15日

概览

阶段
不适用
干预措施
Treatment Interruption Arm
疾病 / 适应症
HIV/AIDS
发起方
University of California, San Francisco
入组人数
40
试验地点
1
主要终点
CD4+ T cell decline
状态
招募中
最后更新
3个月前

概览

简要总结

The goal of this study is to understand the interaction between HIV and the host at the earliest stages when HIV medications are paused. Volunteers with HIV will interrupt antiretroviral therapy (ART) and then have intensive studies preformed two to three times per week. Most will resume therapy within three weeks, even if the virus does not rebound during this time.

详细描述

In this study, people living with HIV will undergo intensive sampling prior to and following an interruption of their antiretroviral therapy (ART). Individuals will be asked to resume ART once the virus is detectable, or after approximately three weeks if the virus remains undetectable. Individuals who were able to control their virus before ART ("controllers") will be able to participate in an extended treatment interruption and have less restrictive ART restart criteria. The overall goal of the study is to characterize the interaction between the host and the virus at the earliest stages of virus replication and to identify predictors of rebound before virus becomes detectable.

注册库
clinicaltrials.gov
开始日期
2020年10月15日
结束日期
2028年6月1日
最后更新
3个月前
研究类型
Interventional
研究设计
Single Group
性别
All

研究者

入排标准

入选标准

  • Willing and able to provide written informed consent
  • Age \>= 18
  • Documented HIV infection
  • Antiretroviral therapy for at least 12 months
  • Screening plasma HIV RNA levels below level of detection (\< 40-75 copies/mL), and all available determinations in past 12 months also below level of detection (blips allowed)
  • Screening CD4+ T-cell count \>350 cells/uL
  • If of childbearing potential, willing to use two methods of contraception
  • Willing to receive counseling regarding HIV transmission risk mitigation

排除标准

  • Pregnant or plans to become pregnant during the course of the study
  • Active hepatitis B, defined as (1) positive sAg or (2) positive cAb with negative sAb and positive HBV DNA
  • Active hepatitis C, defined as positive Hep C Ab with positive HCV RNA
  • Use of a non-nucleoside reverse transcriptase inhibitor and unable to switch regimen
  • Significant cardiovascular or cerebrovascular disease
  • Recent or prior (within past 5 years) malignancy
  • Severe kidney disease (CrCl \< 50 mL/min via Cockroft-Gault method)
  • Severe hepatic impairment (Child-Pugh Class C) or unstable liver disease
  • Concurrent treatment with immunomodulatory drugs
  • Unable or unwilling to use barrier protection or pre-exposure prophylaxis (PrEP) to prevent HIV transmission with sexual partners not known to be HIV-infected

研究组 & 干预措施

Treatment Interruption Arm

干预措施: Treatment Interruption Arm

结局指标

主要结局

CD4+ T cell decline

时间窗: Week 0 through Month 6

The proportion of participants with confirmed decreases in CD4+ T cell count below 350 cells/uL

Acute retroviral syndrome

时间窗: Week 0 through Month 6

The proportion of participants developing acute retroviral syndrome

Failure to re-suppress

时间窗: Week 0 through Month 12

The proportion of participants who fail to re-suppress to plasma HIV RNA levels \<50 copies/mL after re-initiating ART

Time to rebound

时间窗: Week 0 through Month 6

The time between the treatment interruption and plasma HIV RNA \>200 copies/mL

研究点 (1)

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