New antibiotics in clinical trials for Clostridium difficile

被引:3
|
作者
Slayton, Eric T. [1 ]
Hay, Abigail S. [2 ,3 ]
Babcock, Charles K. [2 ]
Long, Timothy E. [1 ,4 ]
机构
[1] Marshall Univ, Sch Pharm, Dept Pharmaceut Sci & Res, Huntington, WV 25755 USA
[2] Marshall Univ, Sch Pharm, Dept Pharm Practice Adm & Res, Huntington, WV USA
[3] St Marys Hosp, Dept Pharm, Huntington, WV USA
[4] Marshall Univ, Joan C Edwards Sch Med, Dept Biochem & Microbiol, Huntington, WV 25755 USA
关键词
Infectious disease; Clostridium difficile; CDAD; CDI; antibiotic; cadazolid; LFF571; ridinilazole; surotomycin; IN-VITRO ACTIVITIES; TOXIN PRODUCTION; HAMSTER MODEL; REDUCED SUSCEPTIBILITY; ANTIMICROBIAL ACTIVITY; CYCLIC LIPOPEPTIDE; GUT MICROBIOTA; DOUBLE-BLIND; SMT19969; LFF571;
D O I
10.1080/14787210.2016.1211931
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Introduction: There are limited number of approved therapies for C. difficile infections (CDIs) and new treatments are needed to decrease recurrence rates. Over the past 5years, four novel antibiotics have been evaluated in clinical trials that offer distinct advantages over existing therapies for the treatment of CDI.Areas covered: This article reviews the preclinical and clinical studies of cadazolid, LFF571, ridinilazole, and surotomycin. The advantages that these antibiotics may have in the treatment of CDI is compared with current therapies metronidazole, vancomycin, and fidaxomicin.Expert commentary: The antibiotics examined have the potential to improve rates of CDI treatment without recurrence. We anticipate that one or more of these medications will be approved within five years.
引用
收藏
页码:789 / 800
页数:12
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