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Comparative Study
. 1999 Sep;43(9):2236-9.
doi: 10.1128/AAC.43.9.2236.

In vitro activities of BMS-207147 against over 600 contemporary clinical bloodstream isolates of Candida species from the SENTRY Antimicrobial Surveillance Program in North America and Latin America

Affiliations
Comparative Study

In vitro activities of BMS-207147 against over 600 contemporary clinical bloodstream isolates of Candida species from the SENTRY Antimicrobial Surveillance Program in North America and Latin America

D J Diekema et al. Antimicrob Agents Chemother. 1999 Sep.

Abstract

We compared the in vitro activity of BMS-207147, an investigational triazole, with those of itraconazole and fluconazole against 613 clinical bloodstream isolates of Candida spp. collected from SENTRY participating hospitals during 1997 and 1998. Overall, BMS-207147 was the most active azole against all Candida spp. While both BMS-207147 and itraconazole displayed a stepwise decrease in activity against isolates for which the fluconazole MICs were elevated, BMS-207147 had two- to fourfold greater activity than itraconazole both against Candida spp. that were dose-dependently fluconazole susceptible and against those that were fluconazole resistant.

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References

    1. Bartroli J, Turmo E, Alguero M. New azole antifungals. 3. Synthesis and antifungal activity of 3-substituted-4(3H)-quinozolinones. J Med Chem. 1998;41:1868–1882. - PubMed
    1. Espinel-Ingroff A. Abstracts of the 38th Interscience Conference on Antimicrobial Agents and Chemotherapy. Washington, D.C: American Society for Microbiology; 1998. Evaluation of antifungal susceptibility testing parameters for amphotericin B, itraconazole, voriconazole, SCH56592, and BMS-207147 against Aspergillus spp., abstr. J-7; p. 452.
    1. Espinel-Ingroff A, Palacio A, Carrillo-Munoz A. Abstracts of the 38th Interscience Conference on Antimicrobial Agents and Chemotherapy. Washington, D.C: American Society for Microbiology; 1998. In vitro activity of the new triazole BMS-207147 against Aspergillus spp., Candida spp., and emerging mold pathogens: a comparative study, abstr. F-154; p. 271.
    1. Fung-Tomc J C, Huczko E, Minassian B, Bonner D P. In vitro activity of a new oral triazole, BMS-207147 (ER-30346) Antimicrob Agents Chemother. 1998;42:313–318. - PMC - PubMed
    1. Hata K, Kimura J, Miki H, Toyosawa T, Moriyama M, Katsu K. Efficacy of ER-30346, a novel oral triazole antifungal agent, in experimental models of aspergillosis, candidiasis, and cryptococcosis. Antimicrob Agents Chemother. 1996;40:2243–2247. - PMC - PubMed

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