棘白菌素
金念珠菌
抗真菌药
抗真菌
念珠菌感染
光滑假丝酵母
侵袭性念珠菌病
抗真菌药
医学
白霉素类
真菌病原
重症监护医学
食管念珠菌病
药品
药理学
氟康唑
卡斯波芬金
病菌
免疫学
皮肤病科
人类免疫缺陷病毒(HIV)
病毒性疾病
摘要
Abstract: Invasive candidiasis (IC), due to the yeast pathogen Candida , is still a major cause of in-hospital morbidity and mortality. The limited number of antifungal drug classes and the emergence of multi-resistant Candida species, such as Candida auris and some Candida glabrata isolates, is concerning. However, recent advances in antifungal drug development provide promising perspectives for the therapeutic approach of IC. Notably, three novel antifungal agents, currently in Phase II/III clinical trials, are expected to have an important place for the treatment of IC in the future. Rezafungin is a novel echinocandin with prolonged half-life. Ibrexafungerp and fosmanogepix are two first-in-class antifungal drugs with broad spectrum activity against Candida spp., including C. auris and echinocandin-resistant species. These novel antifungal agents also represent interesting alternative options because of their acceptable oral bioavailability (ibrexafungerp and fosmanogepix) or their large interdose interval (once weekly intravenous administration for rezafungin) for prolonged and/or outpatient treatment of complicated IC. This review discusses the potential place of these novel antifungal drugs for the treatment of IC considering their pharmacologic properties and their preclinical and clinical data. Keywords: Candida, candidemia, rezafungin, ibrexafungerp, fosmanogepix, oteseconazole, tetrazoles, T-2307, antifungal therapy
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