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Antimicrobial Agents and Chemotherapy, December 1998, p. 3242-3244, Vol. 42, No. 12
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
In Vitro Susceptibilities of Candida
Bloodstream Isolates to the New Triazole Antifungal Agents BMS-207147,
Sch 56592, and Voriconazole
M. A.
Pfaller,1,*
S. A.
Messer,1
R. J.
Hollis,1
R. N.
Jones,1
G. V.
Doern,1
M. E.
Brandt,2 and
R.
A.
Hajjeh2
Department of Pathology, University of Iowa
College of Medicine, Iowa City, Iowa,1 and
Mycotic Diseases Branch, Centers for Disease Control and
Prevention, Atlanta, Georgia2
Received 16 July 1998/Returned for modification 21 August
1998/Accepted 15 September 1998
BMS-207147, Sch 56592, and voriconazole are three new
investigational triazoles with broad-spectrum antifungal activity. The in vitro activities of these three agents were compared with those of
itraconazole and fluconazole against 1,300 bloodstream isolates of
Candida species obtained from over 50 different medical
centers in the United States. The MICs of all of the antifungal drugs were determined by broth microdilution tests performed according to the
National Committee for Clinical Laboratory Standards method using RPMI
1640 as a test medium. BMS-207147, Sch 56592, and voriconazole were all
quite active against all Candida sp. isolates (MICs for 90% of the isolates tested [MIC90s], 0.5, 1.0, and 0.5 µg/ml, respectively). Candida albicans was the most
susceptible species (MIC90s, 0.03, 0.06, and 0.06 µg/ml,
respectively), and C. glabrata was the least susceptible
(MIC90s, 4.0, 4.0, and 2.0 µg/ml, respectively). BMS-207147, Sch 56592, and voriconazole were all more active than itraconazole and fluconazole against C. albicans, C. parapsilosis, C. tropicalis, and C. krusei. There existed a clear rank order of in vitro activity of
the five azoles examined in this study when they were tested versus
C. glabrata: voriconazole > BMS-207147 = Sch
56592 = itraconazole > fluconazole (MIC90s, 2.0, 4.0, 4.0, 4.0, and 64 µg/ml, respectively). For isolates of
Candida spp. with decreased susceptibility to both
itraconazole and fluconazole, the MICs of BMS-207147, Sch 56592, and
voriconazole were also elevated. These results suggest that BMS-207147,
Sch 56592, and voriconazole all possess promising antifungal activity
and that further in vitro and in vivo investigations are warranted to
establish the clinical value of this improved potency.
*
Corresponding author. Mailing address: Medical
Microbiology Division, C606 GH, Department of Pathology, University of
Iowa College of Medicine, Iowa City, IA 52242. Phone: (319) 394-9566. Fax: (319) 356-4916. E-mail: michael-pfaller{at}uiowa.edu.
Antimicrobial Agents and Chemotherapy, December 1998, p. 3242-3244, Vol. 42, No. 12
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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