Ridinilazole: a novel antimicrobial for Clostridium difficile infection

被引:13
作者
Cho, Jonathan C. [1 ]
Crotty, Matthew P. [2 ]
Pardo, Joe [3 ]
机构
[1] Univ Texas Tyler, Coll Pharm, 3900 Univ Blvd, Tyler, TX 75799 USA
[2] Methodist Dallas Med Ctr, Dept Pharm, Dallas, TX USA
[3] North FL South GA Vet Hlth Syst, Dept Pharm, Gainesville, FL USA
来源
ANNALS OF GASTROENTEROLOGY | 2019年 / 32卷 / 02期
关键词
Ridinilazole; Clostridium difficile; infectious diarrhea; IN-VITRO ACTIVITIES; HAMSTER MODEL; HIGH-RISK; SMT19969; VANCOMYCIN; SUSCEPTIBILITY; FIDAXOMICIN; IMPACT; AGENT; EPIDEMIC;
D O I
10.20524/aog.2018.0336
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Clostridium difficile (C. difficile) infection remains a global healthcare threat worldwide and the limited options available for its treatment are of particular concern. Ridinilazole is one potential future agent, as it demonstrates rapid bactericidal activity against C. difficile. Current studies show that ridinilazole has a lower propensity for collateral damage to the gut microbiome and appears to diminish the production of C. difficile toxins. Results from phase II studies demonstrate that patients receiving ridinilazole had a higher sustained clinical response compared with patients receiving vancomycin (66.7% vs. 42.4%; P=0.0004). Adverse reactions were similar between ridinilazole and vancomycin (40% vs. 56%, respectively), with most being gastrointestinal- related. Nausea (20%) and abdominal pain (12%) were the most commonly reported adverse reactions associated with ridinilazole. Phase II study results are promising and future availability of phase III trial results will help further delineate the role and value of ridinilazole.
引用
收藏
页码:134 / 140
页数:7
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