JMI Laboratories, North Liberty, Iowa, USA
JMI Laboratories, North Liberty, Iowa, USA.
Antimicrob Agents Chemother. 2017 Nov 22;61(12). doi: 10.1128/AAC.01230-17. Print 2017 Dec.
Nafithromycin (WCK 4873), a novel antimicrobial agent of the lactone ketolide class, is currently in phase 2 development for treatment of community-acquired bacterial pneumonia (CABP). A total of 4,739 nonduplicate isolates were selected from a 2014 global surveillance program at medical institutions located in 43 countries within the United States, Europe, Latin America, and the Asia-Pacific region. Nafithromycin and comparator agents were used for susceptibility testing by reference broth microdilution methods. Nafithromycin was active against (MIC, 0.06/>2 μg/ml), including erythromycin-resistant strains exhibiting an inducible clindamycin resistance phenotype (MIC, 0.06/0.06 μg/ml) and telithromycin-susceptible strains (MIC, 0.06/0.06 μg/ml), but it exhibited limited activity against most telithromycin-resistant and clindamycin-resistant isolates that were constitutively resistant to macrolides (MIC, >2/>2 μg/ml). Nafithromycin was very active (MIC, 0.015/0.06 μg/ml) against 1,911 strains, inhibiting all strains, with MIC values of ≤0.25 μg/ml. Telithromycin susceptibility was 99.9% for strains, and nafithromycin was up to 8-fold more potent than telithromycin. Overall, 37.9% of strains were resistant to erythromycin, and 19.7% were resistant to clindamycin. Nafithromycin was highly active against 606 strains (MIC, 0.015/0.015 μg/ml), inhibiting 100.0% of isolates at ≤0.5 μg/ml, and MIC values (0.015/0.015 to 0.03 μg/ml) were similar for the 4 geographic regions. Nafithromycin and telithromycin demonstrated comparable activities against 1,002 isolates and 504 isolates. Overall, nafithromycin showed potent activity against a broad range of contemporary (2014) global pathogens. These results support the continued clinical development of nafithromycin for treatment of CABP.
那氟沙星(WCK4873)是一种新型的内酯酮内酯类抗菌药物,目前处于治疗社区获得性细菌性肺炎(CABP)的 2 期开发阶段。从 2014 年在美国、欧洲、拉丁美洲和亚太地区的 43 个国家的医疗机构进行的全球监测计划中选择了总共 4739 个非重复分离株。采用参考肉汤微量稀释法对那氟沙星和对照剂进行药敏试验。那氟沙星对大多数(MIC,0.06/>2μg/ml)表现出诱导克林霉素耐药表型的红霉素耐药株(MIC,0.06/0.06μg/ml)和对替利霉素敏感的菌株(MIC,0.06/0.06μg/ml)均具有活性,但对大多数对大环内酯类药物固有耐药(MIC,>2/>2μg/ml)且对替利霉素耐药的菌株活性有限。那氟沙星对 1911 株 1 表现出非常强的活性(MIC,0.015/0.06μg/ml),抑制所有菌株,MIC 值均≤0.25μg/ml。替利霉素对 菌株的敏感性为 99.9%,那氟沙星的活性比替利霉素强 8 倍。总体而言,37.9%的 菌株对红霉素耐药,19.7%的菌株对克林霉素耐药。那氟沙星对 606 株 6 表现出高度活性(MIC,0.015/0.015μg/ml),在≤0.5μg/ml 时抑制 100.0%的分离株,MIC 值(0.015/0.015 至 0.03μg/ml)在 4 个地理区域相似。那氟沙星和替利霉素对 1002 株和 504 株 1 表现出相当的活性。总体而言,那氟沙星对广泛的当代(2014 年)全球病原体表现出强大的 活性。这些结果支持那氟沙星继续用于治疗 CABP 的临床开发。