在 I、II 或 III 期临床试验中对革兰氏阴性杆菌有效的抗菌剂。

IF 4.9 2区 医学 Q1 PHARMACOLOGY & PHARMACY
David L Paterson
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引用次数: 0

摘要

简介:抗菌药耐药性是对现代医疗保健的一大威胁,人们通常认为抗生素管道已经 "干涸":专家意见:目前有近 50 种对革兰氏阴性杆菌有效的抗菌药物(28 种小分子药物和 21 种非传统抗菌药物)正在进行临床试验。尽管众所周知,由于临床试验中发现的毒性,这些药物有可能从管道中 "流失"。值得注意的是,由于缺乏用于大型 III 期临床试验的资金,因此可能无法针对与抗菌药耐药性导致的生命损失最相关的适应症(如呼吸机相关性肺炎)进行试验。非传统抗菌药物在临床开发中面临一些问题,如缺乏现成可靠的药敏试验,以及可能需要进行优效试验而非劣效试验。最重要的是,在临床开发过程中,必须制定具体计划,让新的抗菌药物进入世界上革兰阴性杆菌耐药性最常见的地区。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antibacterial agents active against Gram Negative Bacilli in phase I, II, or III clinical trials.

Introduction: Antimicrobial resistance is a major threat to modern healthcare, and it is often regarded that the antibiotic pipeline is 'dry.'

Areas covered: Antimicrobial agents active against Gram negative bacilli in Phase I, II, or III clinical trials were reviewed.

Expert opinion: Nearly 50 antimicrobial agents (28 small molecules and 21 non-traditional antimicrobial agents) active against Gram-negative bacilli are currently in clinical trials. These have the potential to provide substantial improvements to the antimicrobial armamentarium, although it is known that 'leakage' from the pipeline occurs due to findings of toxicity during clinical trials. Significantly, a lack of funding for large phase III clinical trials is likely to prevent trials occurring for the indications most relevant to loss of life attributed to antimicrobial resistance such as ventilator-associated pneumonia. Non-traditional antimicrobial agents face issues in clinical development such as a lack of readily available and reliable susceptibility tests, and the potential need for superiority trials rather than non-inferiority trials. Most importantly, concrete plans must be made during clinical development for access of new antimicrobial agents to areas of the world where resistance to Gram negative bacilli is most frequent.

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来源期刊
CiteScore
10.00
自引率
0.00%
发文量
71
审稿时长
6-12 weeks
期刊介绍: Expert Opinion on Investigational Drugs (ISSN 1354-3784 [print], 1744-7658 [electronic]) is a MEDLINE-indexed, peer-reviewed, international journal publishing review articles and original papers on drugs in preclinical and early stage clinical development, providing expert opinion on the scope for future development. The Editors welcome: Reviews covering preclinical through to Phase II data on drugs or drug classes for specific indications, and their potential impact on future treatment strategies Drug Evaluations reviewing the clinical and pharmacological data on a particular drug Original Research papers reporting the results of clinical investigations on agents that are in Phase I and II clinical trials The audience consists of scientists, managers and decision-makers in the pharmaceutical industry, and others closely involved in R&D.
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