Cephalosporins currently in early clinical trials for the treatment of bacterial infections

被引:11
|
作者
Long, Timothy E. [1 ]
Williams, Justin T. [2 ,3 ]
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 25755 USA
[3] St Marys Hosp, Huntington, WV 25702 USA
关键词
antibacterial; ceftolozane; cephalosporin; Enterobacteriaceae; MRSA; Pseudomonas; beta-lactam; IN-VITRO ACTIVITY; GRAM-NEGATIVE BACTERIA; PSEUDOMONAS-AERUGINOSA; CEFTAZIDIME-AVIBACTAM; CEFTAROLINE FOSAMIL; BETA-LACTAMASES; CEFTOLOZANE-TAZOBACTAM; ANTIMICROBIAL ACTIVITY; VIVO ACTIVITIES; EFFLUX PUMPS;
D O I
10.1517/13543784.2014.930127
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Healthcare-associated infections caused by multi-drug resistant bacteria remain a major cause of worldwide mortality. With the recent approval of agents such as hetero-resistant cocci (i.e., ceftaroline, ceftobiprole, telavancin) for the treatment of Gram-positive infections by and drugs like fidaxomicin for treating Clostridium difficile, present-day research on antibacterials has largely shifted to developing interventions for diseases caused by Gram-negative bacilli. Cephalosporins have gained significant interest as antipseudomonals to be used in hospitals for treating device-and procedure-associated infections. With extended-spectrum activity against many enterobacterial pathogens, the introduction of new antipseudomonal cephalosporin-based treatments will mark a significant advancement in the management of hospital-borne diseases. Areas covered: The following review examines the present-day status of investigational cephalosporins currently in preclinical, Phase I and Phase II stage development. The article focuses specifically on treatments used for healthcare-associated infections due to Gram-negative bacteria. Expert opinion: There is an urgent need for new antimicrobials to treat nosocomial infections due to multi-drug resistant Gram-negative bacteria. The impending approvals of antipseudomonal cephalosporins co-formulated with a beta-lactamase inhibitor will allow clinicians to treat more hetero-resistant infections with cephalosporins, while avoiding the use of more toxic agents such as colistin. The growing interest in developing new beta-lactamase inhibitor combinatorial treatments with approved beta-lactam antibiotics is anticipated to decrease the number of novel cephalosporins entering clinical trials this decade.
引用
收藏
页码:1375 / 1387
页数:13
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