白霉素类
药效学
抗真菌
抗真菌药
药理学
抗药性
耐受性
药品
抗真菌药
药物作用
生物
医学
药代动力学
伏立康唑
微生物学
卡斯波芬金
不利影响
出处
期刊:Journal of Fungi
[Multidisciplinary Digital Publishing Institute]
日期:2022-08-16
卷期号:8 (8): 857-857
被引量:43
摘要
Several new antifungals are currently in late-stage development, including those with novel pharmacodynamics/mechanisms of action that represent new antifungal classes (manogepix, olorofim, ATI-2307, GR-2397). Others include new agents within established classes or with mechanisms of action similar to clinically available antifungals (ibrexafungerp, rezafungin, oteseconazole, opelconazole, MAT2203) that have been modified in order to improve certain characteristics, including enhanced pharmacokinetics and greater specificity for fungal targets. Many of the antifungals under development also have activity against Candida and Aspergillus strains that have reduced susceptibility or acquired resistance to azoles and echinocandins, whereas others demonstrate activity against species that are intrinsically resistant to most clinically available antifungals. The tolerability and drug-drug interaction profiles of these new agents also appear to be promising, although the number of human subjects that have been exposed to many of these agents remains relatively small. Overall, these agents have the potential for expanding our antifungal armamentarium and improving clinical outcomes in patients with invasive mycoses.
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