In Vitro Antifungal Activity of Ibrexafungerp (SCY-078) Against Contemporary Blood Isolates From Medically Relevant Species of Candida: A European Study

Abstract

Background:

Ibrexafungerp (SCY-078) is the newest oral and intravenous antifungal drug with broad activity, currently undergoing clinical trials for invasive candidiasis.

Objective:

The aim of this study was to assess the in vitro activity of ibrexafungerp and comparators against a collection of 434 European blood isolates of Candida.

Methods:

Ibrexafungerp, caspofungin, fluconazole, and micafungin minimum inhibitory concentrations (MICs) were collected from 12 European laboratories for 434 blood isolates, including 163 Candida albicans, 108 Candida parapsilosis, 60 Candida glabrata, 40 Candida tropicalis, 29 Candida krusei, 20 Candida orthopsilosis, 6 Candida guilliermondii, 2 Candida famata, 2 Candida lusitaniae, and 1 isolate each of Candida bracarensis, Candida catenulata, Candida dubliniensis, and Candida kefyr. MICs were determined by the EUCAST broth microdilution method, and isolates were classified according to recommended clinical breakpoints and epidemiological cutoffs. Additionally, 22 Candida auris from different clinical specimens were evaluated.

Results:

Ibrexafungerp MICs ranged from 0.016 to ≥8 mg/L. The lowest ibrexafungerp MICs were observed for C. albicans (geometric MIC 0.062 mg/L, MIC range 0.016–0.5 mg/L) and the highest ibrexafungerp MICs were observed for C. tropicalis (geometric MIC 0.517 mg/L, MIC range 0.06–≥8 mg/L). Modal MICs/MIC₅₀s (mg/L) against Candida spp. were 0.125/0.06 for C. albicans, 0.5/0.5 for C. parapsilosis, 0.25/0.25 for C. glabrata, 0.5/0.5 for C. tropicalis, 1/1 for C. krusei, 4/2 for C. orthopsilosis, and 0.5/0.5 for C. auris. Ibrexafungerp showed activity against fluconazole- and echinocandin-resistant isolates. If adopting wild-type upper limits, a non-wild-type phenotype for ibrexafungerp was only observed for 16/434 (3.7%) isolates: 11 (4.6%) C. parapsilosis, 4 (5%) C. glabrata, and 1 (2.5%) C. tropicalis.

Conclusion:

Ibrexafungerp showed a potent in vitro activity against Candida.

Introduction

Invasive candidiasis (IC) is the most common healthcare-associated invasive mycosis, being a major cause of human morbidity and mortality. Candida albicans is the most prevalent etiology, but other species, such as Candida glabrata, Candida parapsilosis, Candida krusei (Pichia kudriavzevii), and, more recently, Candida auris, are increasing causes of IC. These emergent species are usually less susceptible to current antifungal drugs. Although Candida isolates displaying antifungal resistance are still uncommon, they are increasingly reported worldwide. Therapy of IC is an unsolved clinical challenge and, for this reason, monitoring antifungal susceptibility patterns and resistance mechanisms is of utmost importance. Moreover, new antifungal drugs are needed as the number of available antifungal drug classes, and particularly those for oral administration, is limited (Arendrup and Patterson, 2017; Quindós et al., 2018; Fuller et al., 2019; Pfaller et al., 2019).

Ibrexafungerp (formerly SCY-078) is a semisynthetic triterpenoid glycoside derived from enfumafungin, which is structurally different from echinocandins and form a new class of antifungal drugs called “fungerps” that strongly inhibit fungal 1,3-β-glucan synthase (Davis et al., 2020). Even ibrexafungerp and echinocandins share similar mechanisms of action, and their binding sites to the target enzyme is not the same, resulting in very limited cross-resistance (Jiménez-Ortigosa et al., 2017; Pfaller et al., 2017). Ibrexafungerp displays significant in vitro and in vivo activities against azole- and echinocandin-resistant isolates of Candida species, including biofilm-forming strains (Jiménez-Ortigosa et al., 2014; Pfaller et al., 2017; Schell et al., 2017; Gamal et al., 2021).

Ibrexafungerp aims to be the first orally and intravenously available glucan synthase inhibitor useful in the treatment of life-threatening fungal infections (Davis et al., 2020) as well as superficial ones, such as vulvovaginal candidiasis (Schwebke et al., 2021; Sobel et al., 2022). Currently, there are 13 listed clinical trials for ibrexafungerp, eight of which have been completed (https://ClinicalTrials.gov/; accessed on March 8, 2022).

In the current study, we have determined the anti-Candida in vitro activity of ibrexafungerp, caspofungin, fluconazole, and micafungin against 434 European Candida blood isolates analyzed in 12 European laboratories.

Materials and Methods

Microorganisms

In vitro susceptibility of a collection of 434 Candida blood isolates (2016–2018) from 434 patients was determined at 12 laboratories from Belgium, Germany, Italy, Portugal, and Spain. Each laboratory studied its own clinical isolates. The collection included 163 C. albicans, 108 C. parapsilosis, 60 C. glabrata, 40 C. tropicalis, 29 C. krusei, 20 Candida orthopsilosis, 6 Candida guilliermondii (Meyerozyma guilliermondii), 2 Candida famata (Debaryomyces hansenii), 2 Candida lusitaniae (Clavispora lusitaniae), and 1 isolate each of Candida bracarensis, Candida catenulata (Diutina catenulata), Candida dubliniensis, and Candida kefyr (Kluyveromyces marxianus). Additionally, 22 C. auris from different clinical specimens were evaluated: Eight isolates were from blood, seven from oral specimens, and 7 from urine (Ruiz-Gaitán et al., 2017; Ruiz-Gaitán et al., 2018). Isolates were identified by phenotypic methods, MALDI-TOF (proteomic method), and, when needed, internal transcribed spacer (ITS) sequencing (genotypic method) (Miranda-Zapico et al., 2011). C. parapsilosis ATCC 22019 and C. krusei ATCC 6258 were included as quality control (QC) strains. Reference strain C. albicans ATCC 64550 was also included as recommended by EUCAST for detecting variation in echinocandin activities. Prior to testing, each isolate was cultured onto Sabouraud dextrose agar and/or CHROMagar Candida medium (Becton Dickinson, Sparks, MD, USA) to ensure purity and viability. QC and reference strain were included every testing day and all their results were within published ranges.

Antifungal Drugs and Susceptibility Testing

All isolates were tested for in vitro susceptibility to ibrexafungerp, caspofungin, fluconazole, and micafungin using the EUCAST broth microdilution method (Arendrup et al., 2020a; Arendrup et al., 2020b; EUCAST, 2020; EUCAST, 2021). The reference powder of ibrexafungerp was obtained from the manufacturer (SCYNEXIS Inc., Jersey City, NJ, USA). Stock solutions were prepared in dimethyl sulfoxide (DMSO), and the final range of ibrexafungerp, caspofungin, and micafungin concentrations tested was 0.008 to 8 mg/L except for fluconazole, which ranged from 0.125 to 128 mg/L. The EUCAST method was performed by using RPMI 1640 with 2% glucose and buffered to pH 7.0 with 0.165 M morpholinopropane sulphate (MOPS). Panels were inoculated with a final standardized cell concentration of 0.5–2.5 × 10⁵ cells/ml. Panels were read spectrophotometrically at 450 nm after 24 h of incubation at 36 ± 1°C. Although caspofungin presents excessive inter-laboratory variation in minimum inhibitory concentration (MIC) results by the EUCAST broth microdilution method (Espinel-Ingroff et al., 2013), MICs were calculated for comparison purposes.

Data Analysis

MIC values were determined as the lowest concentration of antifungal drug that inhibited 50% of growth compared to that of the growth control. For individual species of Candida for which ten or more isolates were tested, summary descriptive statistics, including MIC ranges, modal MIC (MM) (the most reported MIC), geometric mean MIC (GM), MIC at which 50% of the isolates was inhibited (MIC₅₀), and MIC at which 90% of the isolates was inhibited (MIC₉₀), were calculated for each species and drug. High off-scale MIC results were converted to the next highest concentration, and low off-scale MIC results were left unchanged. Epidemiological cutoff values (ECVs) were used to differentiate wild-type (WT) (without acquired resistance mechanisms) from non-wild-type (NWT) (may harbor acquired resistance mechanisms) isolates. For antifungal drugs, such as ibrexafungerp and caspofungin, or/and species, such as C. auris and C. orthopsilosis, without EUCAST ECVs, WT upper limits (WTUL) were used as the susceptibility cutoff values and MICs > 2 dilution steps above the MM were regarded as NWT (Table 1). Comparison of efficacy among antifungal drugs was based on MIC₉₀ differences: Those antifungal drugs with a difference of one double dilution were considered to have a similar activity (Wiederhold, 2021). This comparison should not be considered absolute, as other pharmacokinetics and pharmacodynamics (PK/PD) parameters should be taken into account. The study was approved by the Ethics Committee of the Universidad del País Vasco/Euskal Herriko Unibertsitatea (UPV/EHU, Bilbao, Spain, CEIAB Ethics reference number M30_2015_248).

Results

MICs of ibrexafungerp against all species were tested in vitro ranging from 0.016 to ≥8 mg/L (MIC₉₀ 2 mg/L). These values were comparable to those of caspofungin and micafungin (MIC₉₀ 2 mg/L). The lowest ibrexafungerp MICs were observed for C. albicans (GM 0.062 mg/L, MIC range 0.016–0.5 mg/L, MIC₉₀ 0.125 mg/L) and the highest ibrexafungerp MICs were observed for C. tropicalis (GM 0.517 mg/L, MIC range 0.06–≥8 mg/L, MIC₉₀ 2 mg/L) (Table 2). Echinocandins MIC values for C. albicans ranged from ≤ 0.008 mg/L to 2 mg/L for micafungin (MM 0.008 mg/L, GM 0.001 mg/L, MIC₉₀ 0.016 mg/L) and from 0.016 mg/L to 2 mg/L for caspofungin (MM 0.125 mg/L, GM 0.104 mg/L, MIC₉₀ 0.125 mg/L). For the three isolates with elevated caspofungin or/and micafungin MICs, ibrexafungerp MIC range was 0.06 mg/L to 0.25 mg/L. In the current report, ibrexafungerp MICs ranged from 0.016 mg/L to 8 mg/L for 108 C. parapsilosis isolates (MM 0.5 mg/L, GM 0.660 mg/L, MIC₉₀ 4 mg/L) (Table 2). If we consider ibrexafungerp WTULs (>2 mg/L) obtained in this study, 11 C. parapsilosis isolates were NWT (4.6%). These NWT isolates were inhibited by ≤1 mg/L of fluconazole and by ≤4 mg/L of caspofungin or micafungin. We also observed that for six C. parapsilosis NWT (5.6%) and two resistant isolates to fluconazole (0.9%), the MIC range of ibrexafungerp was 0.5–2 mg/L. According to MIC90s, ibrexafungerp showed comparable values with caspofungin (MM 1 mg/L, GM 0.846 mg/L, MIC₉₀ 2 mg/L) and micafungin (MM 2 mg/L, GM 0.933 mg/L, MIC₉₀ 2 mg/L). Moreover, two isolates resistant to micafungin were inhibited by 2 mg/L of ibrexafungerp.

Ibrexafungerp also displayed potent in vitro activity against 60 C. glabrata isolates (MIC range 0.016–8 mg/L, MM 0.25 mg/L, GM 0.322 mg/L, MIC₉₀ 1 mg/L) (Table 2). Sixteen C. glabrata isolates resistant to fluconazole were inhibited by ≤1 mg/L of ibrexafungerp. Among 9 C. glabrata isolates with elevated MICs to caspofungin or/and micafungin, the MIC range for ibrexafungerp was 0.25 mg/L to 4 mg/L with a MIC₅₀ of 1 mg/L. It was notable that whereas the increase in MM between C. glabrata WT and NWT isolates was 4-fold for caspofungin and 63-fold for micafungin, MM values for ibrexafungerp did not increase (Table 3).

In vitro activity of ibrexafungerp was also observed against 40 C. tropicalis blood isolates and MICs ranged from 0.06 mg/L to ≥8 mg/L (MM 0.5 mg/L, GM 0.517 mg/L, MIC₉₀ 2 mg/L) (Table 2). Against 14 C. tropicalis resistant to fluconazole, ibrexafungerp MIC range was 0.25–2 mg/L (MIC₉₀ 1 mg/L).

Moreover, ibrexafungerp showed high in vitro activity against 29 C. krusei (MIC range 0.125–1 mg/L, MM 1 mg/L, GM 0.666 mg/L, MIC₉₀ were 1 mg/L). MIC values of micafungin ranged from 0.03 mg/L to 0.25 mg/L (MM 0.125 mg/L, GM 0.122 mg/L, MIC₉₀ 0.125 mg/L) and from 0.25 mg/L to 1 mg/L for caspofungin (MM 0.5 mg/L, GM 0.465 mg/L, MIC₉₀ 1 mg/L). Additionally, all C. auris isolates were resistant in vitro to fluconazole (MIC ≥ 128 mg/L) while ibrexafungerp showed activity (MIC range 0.5 mg/L to 8 mg/L, MM 0.5 mg/L, GM 0.753 mg/L, MIC₉₀ 2 mg/L) (Table 4). C. auris urinary isolates showed higher MICs (data not shown). Against this species, the activity of ibrexafungerp was similar to the activity of micafungin (MIC range 0.125–>8 mg/L, MM 0.125 mg/L, GM 0.377 mg/L, MIC₉₀ 4 mg/L) and 8-fold more active than caspofungin (MIC range 0.25–>8 mg/L, MM 0.25 mg/L, GM 0.585 mg/L, MIC₉₀ >8 mg/L). Among six isolates with elevated caspofungin or/and micafungin MICs, ibrexafungerp MICs ranged from 0.5 mg/L to 8 mg/L (MIC₅₀ 0.5 mg/L).

MICs of ibrexafungerp were ≤ 1 mg/L for the 2 C. famata isolates and 1 isolate each of C. bracarensis, C. catenulata, C. dubliniensis, and C. kefyr (Table 5). Ibrexafungerp MIC₅₀ was 2 mg/L for the 6 C. guilliermondii blood isolates with a MIC range from 2 to 4 mg/L, being twofold less active than caspofungin or micafungin.

Discussion

The present study aimed to evaluate the in vitro activity of ibrexafungerp against a collection of 434 European blood isolates of Candida. Ibrexafungerp showed a potent in vitro activity against Candida, with MICs ranging from 0.016 to 16 mg/L. The lowest ibrexafungerp MICs were observed against C. albicans and the highest ibrexafungerp MICs were observed against C. tropicalis Moreover, ibrexafungerp also displayed remarkable activity against fluconazole- and echinocandin-resistant isolates.

Five species of Candida (C. albicans, C. parapsilosis, C. glabrata, C. tropicalis, and C. krusei) cause more than 90% of IC (Quindós, 2014; Arendrup and Patterson, 2017; Quindós et al., 2018). C. albicans remains the predominant cause, but there is an evident shift in the etiology, and IC caused by other species less susceptible to current antifungal drugs is becoming more frequent (Fuller et al., 2019; Pfaller et al., 2019). Echinocandins, such as anidulafungin, caspofungin, and micafungin, are considered first-line therapy for IC because they possess fungicidal activity against Candida (Gil-Alonso et al., 2015a; Gil-Alonso et al., 2015b). However, emergence of azole- and echinocandin-resistant [multidrug-resistant (MDR)] isolates has been reported for C. auris, C. glabrata, C. guilliermondii, C. lusitaniae, and C. parapsilosis (Lortholary et al., 2011; Pemán et al., 2012; Pfaller et al., 2012; Alexander et al., 2013; Pham et al., 2014; Dudiuk et al., 2017; Ruiz-Gaitán et al., 2019; Tortorano et al., 2021). MDR Candida isolates complicate clinical decision-making and are associated with treatment failure and high mortality rates (Lortholary et al., 2011; Alexander et al., 2013; Shields et al., 2013; Quindós et al., 2018; Tortorano et al., 2021).

Ibrexafungerp is a novel orally bioavailable semi-synthetic derivative of the terpenoid enfumafungin that inhibits glucan synthase, decreasing 1,3-β-D-glucan polymers and weakening fungal cell wall (Jiménez-Ortigosa et al., 2014; Pfaller et al., 2017; Schell et al., 2017; Davis et al., 2020). The current study that has evaluated European blood isolates confirms and extends the observations published in previous studies (Pfaller et al., 2013; Jiménez-Ortigosa et al., 2014; Berkow et al., 2017; Larkin et al., 2017; Marcos-Zambrano et al., 2017; Pfaller et al., 2017; Schell et al., 2017; Nunnally et al., 2019; Gamal et al., 2021). However, these previous studies have mostly tested American isolates. Our study with European isolates is in line with the conclusion that ibrexafungerp displays potent in vitro activity against the most clinically relevant species of Candida.

Ibrexafungerp showed an excellent activity against the C. albicans isolates included in the present study (MICs range 0.016–0.5 mg/L). These results confirm previous findings by other authors, such as Jiménez-Ortigosa et al. (2014); Schell et al. (2017), and Mesquida et al. (2021), demonstrating that ibrexafungerp showed activity against most FKS-mediated echinocandin-resistant C. albicans and against azole-resistant C. albicans.

Although there are no clinical breakpoints (CBPs) or ECVs available for ibrexafungerp, the study by Mesquida et al. (2022) as well as the present work have proposed WTULs. There are no differences in the proposed limits for C. glabrata (1 mg/L). However, our study suggests higher WTUL for C. albicans (0.5 mg/L vs. 0.25 mg/L by Mesquida et al.), for C. parapsilosis and C. tropicalis (2 mg/L vs. 1 mg/L by Mesquida et al.), and for C. krusei (4 mg/L vs. 2 mg/L by Mesquida et al.).

C. parapsilosis is the first or second etiology of IC in China, Japan, Latin America, and the Mediterranean countries of Africa, Asia, and Europe, such as Italy, Portugal, and Spain (Quindós et al., 2018). In the current report, ibrexafungerp MICs ranged from 0.016 mg/L to 8 mg/L. Our results are in accordance to those by Marcos-Zambrano et al. (2017). In both studies, ibrexafungerp displayed remarkably lower MICs than micafungin against C. parapsilosis. Although Mesquida et al. (2022) did not differentiate among C. parapsilosis species complex, they also reported lower MICs for ibrexafungerp than for echinocandins. These high MIC values reported for echinocandins against C. parapsilosis have been associated with substitutions in the hs1 region of FKS1 (Garcia-Effron et al., 2008; Dudiuk et al., 2017; Marcos-Zambrano et al., 2017; Mesquida et al., 2022). Schell et al. (2017) also reported lower ibrexafungerp MIC₉₀ values for 19 C. parapsilosis blood isolates (0.25 mg/L) compared with echinocandins, suggesting that changes in FKS1 may not affect the capacity of ibrexafungerp to inhibit glucan synthase in this species.

C. glabrata has increased its etiological importance in IC in Australia, Canada, the USA, and countries in Central and Northern Europe, such as Belgium and Germany (Quindós, 2014; Trouvé et al., 2017; Quindós et al., 2018). In our study, ibrexafungerp displayed potent activity (MIC range 0.016–8 mg/L) also against fluconazole-resistant isolates. No cross-resistance has been found between ibrexafungerp and fluconazole, as previously noted by Marcos-Zambrano et al. (2017). The incidence of echinocandin resistance in C. glabrata is generally considered low, approximately 3%–4%, but can be as high as 30% in specific institutions (Alexander et al., 2013; Pham et al., 2014; Arendrup and Patterson, 2017). In the current study, ibrexafungerp MIC was ≤4 mg/L against four C. glabrata resistant to both fluconazole and micafungin. Pfaller et al. (2013) found similar results to ours but, in their report, ibrexafungerp was 8-fold more active than caspofungin against C. glabrata. Furthermore, ibrexafungerp showed activity against 31 C. glabrata strains with mutations in the hs of FKS1 or FKS2 (MIC ≤ 2 mg/L) and against 14 strains resistant to both caspofungin and fluconazole. In a later study by the same authors (Pfaller et al., 2017), 20 out of 25 FKS mutant C. glabrata isolates (80%) were NWT to one or more echinocandins, but only six (24%) were NWT to ibrexafungerp. Isolates of C. glabrata for which the ibrexafungerp MIC was > 2 mg/L (NWT) all were NWT and either intermediate or resistant to anidulafungin, caspofungin, and micafungin. In our study, 3 out of 4 isolates potentially NWT for ibrexafungerp were inhibited by ≤1 mg/L of caspofungin and one by 0.03 mg/L of micafungin. However, three of these four ibrexafungerp NWT isolates were resistant to micafungin.

Schell et al. (2017) evaluated 34 echinocandin-resistant C. glabrata isolates along with 34 paired control C. glabrata isolates, observing that ibrexafungerp MICs for individual C. glabrata isolates tended to be three to five dilutions higher than those for the echinocandins. However, ibrexafungerp MICs trended in agreement with those for the echinocandins. These authors detected that C. glabrata isolates with FKS1 or FKS2 mutations or echinocandin resistance were inhibited by ≤4 mg/L of ibrexafungerp. Nunnally et al. (2019) also reported good ibrexafungerp activity against 89 C. glabrata isolates with FKS1 or FKS2 mutations that conferred resistance to at least one echinocandin. Ibrexafungerp MIC values ranged from <0.03 mg/L to 4 mg/L while caspofungin and micafungin MICs ranged from 0.03 to >16 mg/L and 0.008 to >16 mg/L, respectively. In the study by Mesquida et al. (2022), an isolate of C. glabrata that displayed an ibrexafungerp MIC of 2 mg/L and echinocandin NWT phenotype harbored a mutation at FKS2. The spectrum of resistance mutations found in C. glabrata suggested a partially overlapping but independent binding site for ibrexafungerp relative to echinocandins on glucan synthase as these drugs are structurally dissimilar and interact differently with the target (Jiménez-Ortigosa et al., 2014). Consequently, this potent in vitro activity for ibrexafungerp has been reported against C. glabrata isolates harboring FKS1 and FKS2 point mutations that cause echinocandin resistance (Marcos-Zambrano et al., 2017; Pfaller et al., 2017; Schell et al., 2017; Nunnally et al., 2019; Mesquida et al., 2022). Moreover, the in vitro efficacy of ibrexafungerp has been supported by successful treatments in murine IC caused by C. glabrata resistant to echinocandins (Lepak et al., 2015; Wiederhold et al., 2018). In a murine model of IC caused by C. albicans, C. parapsilosis, or C. glabrata using an oral therapy with ibrexafungerp, Lepak et al. (2015) demonstrated that the AUC/MIC was the best pharmacodynamics parameter predicting clinical response. A MIC ≤ 1 mg/L obtained by CLSI would predict a clinical response using oral ibrexafungerp (Marcos-Zambrano et al., 2017).

In Asia, C. tropicalis was the second etiological agent of IC in many hospitals from China, India, Singapore, Thailand, and Taiwan (Quindós et al., 2018). We observed that ibrexafungerp MICs ranged from 0.06 mg/L to ≥ 8 mg/L for 40 C. tropicalis blood isolates, which confirms the consistently low ibrexafungerp MICs for azole-resistant C. tropicalis reported by Schell et al. (2017). Mesquida et al. (2022) found mutations in the FKS1 gene of two NWT isolates of C. tropicalis that resulted, in both cases, in ibrexafungerp MICs between 0.5 and 1 mg/L.

We observed high activity of ibrexafungerp against 29 C. krusei (MIC range 0.125–1 mg/L). Schell et al. (2017) reported ibrexafungerp MICs for six isolates of C. krusei (MIC range from 0.5 mg/L to 4 mg/L), which were higher than those for the other Candida species. These authors suggested that a naturally occurring unidentified substitution may be responsible for the reduced activity of ibrexafungerp on glucan synthase in C. krusei. However, it is unknown if this translates into clinical failure.

In a recent Spanish nationwide study on candidemia, C. orthopsilosis was the fifth most frequently isolated species, preceding C. krusei (Pemán et al., 2012). In the present study, ibrexafungerp showed good activity against 20 C. orthopsilosis (MIC range 0.06–4 mg/L). To our knowledge, this is the first study on in vitro activity of ibrexafungerp against C. orthopsilosis. The lack of previous reports in this regard precludes comparison. Differences in ibrexafungerp activity against the closely related species C. orthopsilosis and C. parapsilosis highlights the importance of a correct identification of the Candida species involved in invasive infections.

C. auris is an emerging pathogen that has been identified in many countries associated with high mortality and a marked ability to develop resistance to multiple commonly used antifungal agents and to withstand standard infection control practices (Larkin et al., 2017; Ruiz-Gaitán et al., 2017; Ruiz-Gaitán et al., 2018; Ruiz-Gaitán et al., 2019). Data from Larkin et al. (2017) show that the C. auris isolates exhibited multidrug resistance against fluconazole and amphotericin B. Moreover, some isolates also exhibited high MIC values for voriconazole and itraconazole. In the present report, all C. auris isolates were resistant to fluconazole while ibrexafungerp showed notable activity (MIC range 0.5 mg/L to 8 mg/L). The in vitro activity of ibrexafungerp against European C. auris isolates from our study was similar to that described by Berkow et al. (2017) who studied 100 isolates of this species from Asia, Africa, and America. Of note, in the current study, MM values between C. auris WT and NWT isolates increased 64-fold for caspofungin and 4-fold for micafungin, whereas MM values for ibrexafungerp did not change. Interestingly, ibrexafungerp has been shown to be effective in vivo in the treatment of experimental infections with C. auris (Wiederhold et al., 2021).

Ibrexafungerp was twofold less active than caspofungin or micafungin against six C. guilliermondii blood isolates. Accordingly, Mesquida et al. (2022) also found higher ibrexafungerp MICs for 12 C. guilliermondii isolates, from 0.125 to 8 mg/L. Naturally occurring high echinocandins MICs against C. guilliermondii have been recognized since these antifungal agents were first introduced probably in association to substitutions in the hs1 region of FKS1 (Dudiuk et al., 2017; Schell et al., 2017). In addition, Schell et al. (2017) reported that ibrexafungerp MIC ranges for three C. lusitaniae blood isolates were 1 to 2 mg/L and ibrexafungerp MICs for C. lusitaniae were three to five dilutions higher than those for the other species of Candida. Ibrexafungerp MICs for the two isolates of C. lusitaniae (MICs 4 and 8 mg/L) tested in the current study were higher than those observed for the other Candida species.

Aside from emerging resistance, an important limitation of echinocandins is that they must be administered daily by intravenous infusion, potentially prolonging hospital stays for patients undergoing echinocandin therapy and limiting them to inpatient settings in most instances. Of note, Wring et al. (2018) reported that the risk for interactions of ibrexafungerp with drugs metabolized via the cytochrome P450 family of enzymes is low. Ibrexafungerp exhibited concentration- and time-dependent fungicidal activity against C. albicans, C. glabrata, C. krusei, C. parapsilosis, and C. tropicalis in time-kill curve studies (Scorneaux et al., 2017). Moreover, ibrexafungerp has demonstrated efficacy for IC in phase 2 and 3 clinical studies (Spec et al., 2019).

The current study demonstrates that ibrexafungerp shows potent in vitro activity against Candida blood isolates and its activity is comparable to that of micafungin. Ibrexafungerp even exhibits good activity against fluconazole-resistant Candida isolates. Moreover, echinocandin-resistant isolates exhibit ibrexafungerp MICs consistent with those of echinocandin-susceptible isolates. However, direct comparisons of ibrexafungerp MICs with those of other antifungal drugs should be interpreted with caution, as different drugs may produce diverse ranges of MICs and yet have equivalent clinical efficacy because of their differences in bioavailability and in PK/PD properties. Although Pfaller et al. (2013) reported >90% essential agreement between both methods, CLSI and EUCAST, the comparison between our results and those of American authors should consider that the EUCAST method tends to yield higher MICs than CLSI, regardless of the studied species. Although the most clinically relevant species of Candida have been included in the current study, it would be interesting to assess the activity of ibrexafungerp against additional species as well as more NWT isolates.

In conclusion, we demonstrated that ibrexafungerp, a potent inhibitor of glucan synthase, could be an important acquisition to the antifungal toolbox for the therapy of patients suffering from IC caused by MDR species, such as C. auris, C. glabrata, or C. krusei. Considering the excellent pharmacokinetic properties of ibrexafungerp (oral availability and excellent tissue distribution and concentrations) as well as the potent activity observed against the main species causing candidiasis, ibrexafungerp should be regarded as a potential candidate for the therapy of these important diseases.

Funding

This study received funding from SCYNEXIS. The funder was not involved in the study design, collection, analysis, interpretation of data, the writing of the article, or the decision to submit it for publication. CM-A is a recipient of a grant from Fundación ONCE (Oportunidad al Talento). EE, AG, NJ, CM-A, and GQ have received grant support from Consejería de Educación, Universidades e Investigación del Gobierno Vasco (GIC15 IT-990-16), Fondo de Investigación Sanitaria del Gobierno de España (FIS PI11/00203), and UPV/EHU (UFI 11/25). All authors declare no other competing interests.

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