The Evaluation of Subcutaneous Proleukin® (interleukin-2) in a Randomized International Trial:: rationale, design, and methods of ESPRIT

被引:70
作者
Emery, S
Abrams, DI
Cooper, DA
Darbyshire, JH
Lane, HC
Lundgren, JD
Neaton, JD
机构
[1] Univ New South Wales, Natl Ctr HIV Epidemiol & Clin Res, Sydney, NSW 2010, Australia
[2] Univ Calif San Francisco, San Francisco, CA USA
[3] UCL, Med Sch, MRC Clin Trials Unit, London, England
[4] Natl Inst Allergy & Infect Dis, NIH, Bethesda, MD USA
[5] Univ Copenhagen, Hvidovre Hosp, Dept Infect Dis, Copenhagen, Denmark
[6] Univ Minnesota, Sch Publ Hlth, Div Biostat, Minneapolis, MN USA
来源
CONTROLLED CLINICAL TRIALS | 2002年 / 23卷 / 02期
关键词
interleukin-2; HIV; clinical endpoint study;
D O I
10.1016/S0197-2456(01)00179-9
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The Evaluation of Subcutaneous Proleukin(R) in a Randomized International Trial (ESPRIT) is a large ongoing randomized trial of subcutaneous interleukin-2 (IL-2) plus antiretroviral therapy versus antiretroviral therapy alone in patients with HIV (human immunodeficiency virus) disease and CD4 cell counts of at least 300 cells/mm(3). The primary objective is to determine whether the addition of IL-2 to combination antiretroviral therapy improves morbidity and mortality. The aim is to recruit 4000 participants and follow them for an average of 5 years. Eligible subjects will be recruited at 275 investigational sites in 23 countries around the world. Coupled with broad eligibility criteria this will ensure widely applicable results. A range of secondary objectives will also be addressed in this setting that will include the conduct of observational studies and nested substudies with a public health focus. This article describes the rationale supporting the trial in addition to reviewing the study design, coordination, and governance. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:198 / 220
页数:23
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