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首页> 外文期刊>Future microbiology >Iclaprim, a dihydrofolate reductase inhibitor antibiotic in Phase III of clinical development: a review of its pharmacology, microbiology and clinical efficacy and safety
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Iclaprim, a dihydrofolate reductase inhibitor antibiotic in Phase III of clinical development: a review of its pharmacology, microbiology and clinical efficacy and safety

机译:ICLAPRIM,临床发展第III期的二氢醇还原酶抑制剂抗生素:对其药理学,微生物学和临床疗效和安全性的综述

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摘要

Iclaprim is under clinical development for treating acute bacterial skin and skin structure infections (AB-SSSI) and nosocomial pneumonia most often due to Gram-positive bacteria, including infections due to drug-resistant bacteria. In two recent Phase III studies of patients with acute bacterial skin and skin structure infections, intravenous iclaprim 80 mg every 12 h was noninferior to dose-adjusted vancomycin. Additional studies are planned for patients with nosocomial pneumonia. Iclaprim represents an alternative for the treatment of severe skin and pulmonary infections due to Gram-positive bacteria.
机译:Iclaprim正在临床开发,用于治疗急性细菌皮肤和皮肤结构感染(AB-SSSI)和医院肺炎最常见的是由于革兰氏阳性细菌,包括由于耐药细菌引起的感染。 在最近急性细菌皮肤和皮肤结构感染患者的两期研究中,每12小时静脉内ICLAPRIM 80mg不受剂量调节的万古霉素。 针对医院肺炎患者计划额外的研究。 Iclaprim表示由于革兰氏阳性细菌治疗严重的皮肤和肺部感染的替代方案。

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