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临床试验/NCT00000949
NCT00000949已完成3 期

A Randomized, Open-Label, Study of the Impact of Two Doses of Subcutaneous Recombinant IL-2 (Proleukin) on Viral Burden and CD4+ Cell Count in Patients With HIV-1 Infection and CD4+ Cell Counts Greater Than or Equal to 300/mm3

National Institute of Allergy and Infectious Diseases (NIAID)15 个研究点 分布在 1 个国家目标入组 460 人开始时间: 2001年8月31日最近更新:
适应症
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
460
试验地点
15

研究概览

简要总结

The purpose of this study is to examine how rIL-2 affects HIV-positive patients with CD4 counts over 300 cells/mm3 who are on anti-HIV drug therapy. The drug rIL-2 has been shown to increase CD4 cell counts, which help the body fight off HIV.

There is strong evidence that rIL-2 increases CD4 cell counts (cells of the immune system that fight infection). This study examines the effect of 2 different amounts of rIL-2 on CD4 cell count and the amount of HIV in the blood (viral burden).

详细描述

There is substantial evidence that rIL-2 increases CD4+ cell count. Whether or not rIL-2 delays progression to AIDS and extends survival is currently unknown, such clinical benefits of rIL-2 can only be established in a large, long-term, randomized trial. This study examines the effect of two different rIL-2 doses on HIV viral burden and CD4+ cell count and provides additional information on optimal dosing, safety, and antiviral activity of rIL-2.

Patients are randomized to receive one of two subcutaneous (sc) doses of recombinant rIL-2 or no rIL-2. Those patients who take rIL-2 initially receive three courses of treatment. For this study, a course is defined as eight calendar weeks, including the five-day period of sc rIL-2 administration. Additional courses are given (no more frequently than every 6 weeks) in order to maintain a CD4+ count of at least twice its baseline level or at least 1,000 cells/mm3. Follow-up will continue for all patients until a common closing date of 12 months following enrollment of the last patient.

研究设计

研究类型
Interventional
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •You may be eligible for this study if you:
  • •Are HIV-positive.
  • •Agree to practice abstinence or use effective birth control methods during the study.
  • •Are on anti-HIV therapy and have a CD4 count of at least 300 cells/mm
  • •Are at least 18 years old.

排除标准

  • •You will not be eligible for this study if you:
  • •Have a history of progressive diseases.
  • •Have a history of severe autoimmune/inflammatory disease.
  • •Have Crohn's disease.
  • •Are taking antiseizure medications or certain other medications.
  • •Are receiving chemotherapy.
  • •Are pregnant or breast-feeding.
  • •Have ever received rIL-2.

研究者

申办方类型
Nih
责任方
Sponsor

研究点 (15)

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