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Activity of a novel 1,3-beta-D-glucan Synthase Inhibitor, Ibrexafungerp (formerly SCY-078), Against Candida glabrata.
Ghannoum, M; Long, L; Isham, N; Hager, C; Wilson, R; Borroto-Esoda, K; Barat, S; Angulo, D.
  • Ghannoum M; Center for Medical Mycology, Case Western Reserve University and University Hospitals Cleveland Medical Center, Cleveland, OH Mahmoud.ghannoum@case.edu.
  • Long L; Center for Medical Mycology, Case Western Reserve University and University Hospitals Cleveland Medical Center, Cleveland, OH.
  • Isham N; Center for Medical Mycology, Case Western Reserve University and University Hospitals Cleveland Medical Center, Cleveland, OH.
  • Hager C; Center for Medical Mycology, Case Western Reserve University and University Hospitals Cleveland Medical Center, Cleveland, OH.
  • Wilson R; Center for Medical Mycology, Case Western Reserve University and University Hospitals Cleveland Medical Center, Cleveland, OH.
  • Borroto-Esoda K; Scynexis, Inc, Jersey City, New Jersey, USA.
  • Barat S; Scynexis, Inc, Jersey City, New Jersey, USA.
  • Angulo D; Scynexis, Inc, Jersey City, New Jersey, USA.
Antimicrob Agents Chemother ; 63(12)2019 09 09.
Article en En | MEDLINE | ID: mdl-31570395
Ibrexafungerp (formerly SCY-078), a novel glucan synthase inhibitor with oral availability, was evaluated for activity against Candida glabrata Susceptibility of clinical strains to Ibrexafungerp was determined by microdilution and time kill assays. The MIC range against wild type strains was 1-2 µg/mL. IBX was also active against the majority of echinocandin-resistant strains. Time kill studies showed a 4 to 6-log reduction in growth at concentrations of 0.25 to 4 µg/ml at 24 and 48 hr.