Oritavancin: a potential weapon in the battle against serious Gram-positive pathogens

被引:13
作者
Crandon, Jared [1 ]
Nicolau, David P. [1 ,2 ]
机构
[1] Hartford Hosp, Ctr Anti Infect Res & Dev, Ishikari, Hokkaido 06102, Japan
[2] Hartford Hosp, Div Infect Dis, Hartford, CT 06115 USA
关键词
glycopeptide; LY333328; oritavancin; Staphylococcus aureus; vancomycin-resistant Enterococcus;
D O I
10.2217/17460913.3.3.251
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Oritavancin is a lipoglycopeptide antibiotic with activity against aerobic and anaerobic Gram-positive bacteria. Oritavancin separates itself from other glycopeptides through its potent in vitro activity against resistant isolates of Staphylococcus aureus, Enterococcus spp. and Streptococcus spp. Oritavancin possesses a long half-life that should allow, at maximum, once-daily dosing. Currently, oritavancin has completed two Phase III trials and one Phase II trial for the treatment of complicated skin and skin structure infections, and two Phase II trials for the treatment of Gram-positive bacteremia. In all instances, oritavancin displayed favorable outcomes and was noninferior to comparator agents (vancomycin followed by oral cephalexin) when a comparison was made. Further studies are necessary to fully characterize dose and clinical role.
引用
收藏
页码:251 / 263
页数:13
相关论文
共 60 条
[1]   Activities of LY333328 and vancomycin administered alone or in combination with gentamicin against three strains of vancomycin-intermediate Staphylococcus aureus in an in vitro pharmacodynamic infection model [J].
Aeschlimann, JR ;
Allen, GP ;
Hershberger, E ;
Rybak, MJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (11) :2991-2998
[2]   Mechanism of action of oritavancin and related glycopeptide antibiotics [J].
Allen, NE ;
Nicas, TI .
FEMS MICROBIOLOGY REVIEWS, 2003, 26 (05) :511-532
[3]  
[Anonymous], 47 INT C ANT AG CHEM
[4]   The emergence of vancomycin-intermediate and vancomycin-resistant Staphylococcus aureus [J].
Appelbaum, PC .
CLINICAL MICROBIOLOGY AND INFECTION, 2006, 12 :16-23
[5]  
ARHIN F, 2008, ANTIMICROB AGENTS CH
[6]  
ARHIN F, 2007, 17 EUR C CLIN MICR I
[7]  
ARHIN FF, 2007, 47 INT C ANT AG CHEM
[8]   Comparison of inhibitory and bactericidal activities and postantibiotic effects of LY333328 and ampicillin used singly and in combination against vancomycin-resistant Enterococcus faecium [J].
Baltch, AL ;
Smith, RP ;
Ritz, WJ ;
Bopp, LH .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (10) :2564-2568
[9]  
BARCIAMACAY M, 2003, 43 INT C ANT AG CHEM
[10]  
BELLEY A, 2006, 46 INT C ANT AG CHEM