Strategies to improve drug development for sepsis

被引:211
作者
Fink, Mitchell P. [1 ,2 ]
Warren, H. Shaw [3 ,4 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Surg, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Anesthesiol, Los Angeles, CA 90095 USA
[3] Massachusetts Gen Hosp E, Dept Pediat, Infect Dis Units, Charlestown, MA 02129 USA
[4] Massachusetts Gen Hosp E, Dept Med, Charlestown, MA 02129 USA
关键词
TUMOR-NECROSIS-FACTOR; PLATELET-ACTIVATING-FACTOR; FACTOR PATHWAY INHIBITOR; INTERLEUKIN-1 RECEPTOR ANTAGONIST; NITRIC-OXIDE SYNTHASE; BACTERICIDAL/PERMEABILITY-INCREASING PROTEIN; SIGNAL-TRANSDUCTION INHIBITOR; RESPIRATORY-DISTRESS-SYNDROME; CONTROLLED CLINICAL-TRIAL; HUMAN MONOCLONAL-ANTIBODY;
D O I
10.1038/nrd4368
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Sepsis, a common and potentially fatal systemic illness, is triggered by microbial infection and often leads to impaired function of the lungs, kidneys or other vital organs. Since the early 1980s, a large number of therapeutic agents for the treatment of sepsis have been evaluated in randomized controlled clinical trials. With few exceptions, the results from these trials have been disappointing, and no specific therapeutic agent is currently approved for the treatment of sepsis. To improve upon this dismal record, investigators will need to identify more suitable therapeutic targets, improve their approaches for selecting candidate compounds for clinical development and adopt better designs for clinical trials.
引用
收藏
页码:741 / 758
页数:18
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