Background: Rezafungin is an investigational echinocandin under development for the treatment and prevention of invasive fungal infections, with a long half-life in humans (∼130 h) and potent in vitro activity against Aspergillus spp. Our objective was to further evaluate its activity against Aspergillus fumigatus isolates, including azole-resistant isolates and cryptic Aspergillus spp.
Methods: Clinical isolates of Aspergillus were used, including 15 WT and 31 azole-resistant A.
Background: While echinocandins demonstrate excellent efficacy against species in disseminated infections and demonstrate potent minimal inhibitory concentration (MIC) values under standard susceptibility testing conditions, investigation under conditions relevant to the vaginal environment was needed. We assessed the antifungal activity and time-kill kinetics of the novel echinocandin rezafungin (formerly CD101) under such conditions, against species relevant to vulvovaginal candidiasis (VVC).
Methods: Susceptibility testing of fluconazole-susceptible and fluconazole-resistant , , , , and was performed in RPMI at pH 7.
Antimicrob Agents Chemother
November 2017
CD101 is a novel echinocandin with concentration-dependent fungicidal activity and a long half-life (∼133 h in humans, ∼70 to 80 h in mice). Given these characteristics, it is likely that the shape of the CD101 exposure (i.e.
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