首页> 美国卫生研究院文献>Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America >Progress in the Fight Against Multidrug-Resistant Bacteria 2005–2016: Modern Noninferiority Trial Designs Enable Antibiotic Development in Advance of Epidemic Bacterial Resistance
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Progress in the Fight Against Multidrug-Resistant Bacteria 2005–2016: Modern Noninferiority Trial Designs Enable Antibiotic Development in Advance of Epidemic Bacterial Resistance

机译:2005-2016年抗多药耐药细菌的研究进展:现代非劣效性试验设计可在流行性细菌耐药之前促进抗生素的开发

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摘要

From a public health perspective, new antibacterial agents should be evaluated and approved for use before widespread resistance to existing agents emerges. However, for multidrug-resistant pathogens, demonstration of superior efficacy of a new agent over a current standard-of-care agent is routinely feasible only when epidemic spread of these dangerous organisms has already occurred. One solution to enable proactive drug development is to evaluate new antibiotics with improved in vitro activity against MDR pathogens using recently updated guidelines for active control, noninferiority trials of selected severe infections caused by more susceptible pathogens. Such trials are feasible because they enroll patients with infections due to pathogens with a “usual drug resistance” phenotype that will be responsive to widely registered standard-of-care comparator antibiotics. Such anticipatory drug development has constructively reshaped the antibiotic pipeline and offers the best chance of making safe and efficacious antibiotics available to the public ahead of epidemic resistance.
机译:从公共卫生的角度出发,应在对现有抗菌剂产生广泛耐药性之前评估并批准使用新的抗菌剂。但是,对于具有多重耐药性的病原体,只有在已经发生这些危险生物的流行性传播时,证明新药优于目前的护理标准药的常规功效才是常规可行的。实现主动药物开发的一种解决方案是,使用最新更新的主动控制指南(针对由易感性病原体引起的选定严重感染的非劣效性试验)评估对MDR病原体具有增强的体外活性的新抗生素。这样的试验是可行的,因为它们招募了具有“通常耐药性”表型的病原体感染的患者,该表型将对广泛注册的护理标准比较药物产生反应。这种前瞻性的药物开发建设性地重塑了抗生素的生产渠道,并提供了在抗流行病之前向公众提供安全有效的抗生素的最佳机会。

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