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The investigational agent E1210 is effective in treatment of experimental invasive candidiasis caused by resistant Candida albicans.
- Source :
-
Antimicrobial agents and chemotherapy [Antimicrob Agents Chemother] 2015 Jan; Vol. 59 (1), pp. 690-2. Date of Electronic Publication: 2014 Oct 20. - Publication Year :
- 2015
-
Abstract
- The in vitro and in vivo activity of the inositol acyltransferase inhibitor E1210 was evaluated against echinocandin-resistant Candida albicans. E1210 demonstrated potent in vitro activity, and in mice with invasive candidiasis caused by echinocandin-resistant C. albicans, oral doses of 10 and 40 mg E1210/kg of body weight twice daily significantly improved survival and reduced fungal burden compared to those of controls and mice treated with caspofungin (10 mg/kg/day). These results demonstrate the potential use of E1210 against resistant C. albicans infections.<br /> (Copyright © 2015, American Society for Microbiology. All Rights Reserved.)
- Subjects :
- Aminopyridines therapeutic use
Animals
Antifungal Agents therapeutic use
Caspofungin
Dose-Response Relationship, Drug
Drug Resistance, Fungal
Echinocandins pharmacology
Echinocandins therapeutic use
Fluconazole pharmacology
Fluconazole therapeutic use
Isoxazoles therapeutic use
Lipopeptides
Male
Mice
Mice, Inbred ICR
Microbial Sensitivity Tests
Aminopyridines pharmacology
Antifungal Agents pharmacology
Candida albicans drug effects
Candidiasis, Invasive drug therapy
Isoxazoles pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1098-6596
- Volume :
- 59
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Antimicrobial agents and chemotherapy
- Publication Type :
- Academic Journal
- Accession number :
- 25331706
- Full Text :
- https://doi.org/10.1128/AAC.03944-14