AI Article Synopsis

  • - This mini-review analyzes the clinical outcomes and antifungal susceptibility of three new antifungals: fosmanogepix, ibrexafungerp, and rezafungin, based on isolates from clinical trial patients.
  • - Antifungal susceptibility data primarily comes from the CLSI broth microdilution method or a combination of CLSI and EUCAST methodologies, with specific in vitro results reported for fosmanogepix, ibrexafungerp, and rezafungin.
  • - Overall, the findings provide insights into the effectiveness of these antifungals against various fungal species, although not all clinical isolates have corresponding MIC (minimum inhibitory concentration) data available.

Article Abstract

This mini-review summarizes the clinical outcomes and antifungal susceptibility results, where available, for three new antifungals, including fosmanogepix, ibrexafungerp, and rezafungin, against isolates cultured from patients in clinical trials. When reported, most of the data were generated by the Clinical and Laboratory Standards Institute (CLSI) broth microdilution method or by both the CLSI and European Committee on Antimicrobial Susceptibility Testing (EUCAST) methodologies. For fosmanogepix, we summarize the in vitro data for isolates from 9 patients and for spp. cultured from 20 patients in two clinical trials. Ibrexafungerp has also been evaluated in several clinical trials. From conference proceedings, a total of 176 isolates were evaluated in the FURI and CARES studies, including 18 isolates (CARES study). However, MIC data are not available for all clinical isolates. Results from the ReSTORE rezafungin phase 3 clinical study also included in vitro results against spp., but no patients with infections were included. In conclusion, this mini-review summarizes insights regarding clinical outcomes and the in vitro activity of three new antifungals against spp. cultured from patients in clinical trials.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11122255PMC
http://dx.doi.org/10.3390/jof10050362DOI Listing

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