In vitro activities of the new antifungal triazole SCH 56592 against common and emerging yeast pathogens

A broth microdilution method performed in accordance with the National Comm ittee for Clinical Laboratory Standards guidelines was used to compare the in vitro activity of the new antifungal triazole SCH 56592 (SCH) to that of fluconazole (FLC), itraconazole (ITC), and ketoconazole (KETO) against 257 clinical yeast isolates. They included 220 isolates belonging to 12 differ ent species of Candida, 15 isolates each of Cryptococcus neoformans and Sac charomyces cerevisiae, and seven isolates of Rhodotorula rubra. The MICs of SCH at which 50% (MIC50) and 90% (MIC90) of the isolates were inhibited we re 0.06 and 2.0 mu g/ml, respectively. In general, SCH was considerably mor e active than FLC (MIC50 and MIC90 of 1.0 and 64 mu g/ml, respectively) and slightly more active than either ITC (MIC50 and MIC90 of 0.25 and 2.0 mu g /ml, respectively) and KETO (MIC50 and MIC90 of 0.125 and 4.0 mu g/ml, resp ectively). Our in vitro data suggest that SCH has significant potential for clinical development.