Assessment of the In Vitro Antifungal Activity of SCY-078 Against a Collection of C. parapsilosis Clinical Isolates

Abstract Background Global rates of candidemia caused by C. parapsilosis are increasing with differences detected between neonates and adult patients (50% vs. 12%, respectively) and across geographic regions (5% vs. 25% in Iceland and Spain, respectively). SCY-078 is a novel, oral and intravenous, t...

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Published in:Open Forum Infectious Diseases
Main Authors: Barat, Stephen, Angulo, David, Borroto-Esoda, Katyna, Ghannoum, Mahmoud
Format: Article in Journal/Newspaper
Language:English
Published: Oxford University Press (OUP) 2017
Subjects:
Online Access:http://dx.doi.org/10.1093/ofid/ofx163.902
http://academic.oup.com/ofid/article-pdf/4/suppl_1/S368/33612578/ofx163.902.pdf
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spelling croxfordunivpr:10.1093/ofid/ofx163.902 2023-05-15T16:53:08+02:00 Assessment of the In Vitro Antifungal Activity of SCY-078 Against a Collection of C. parapsilosis Clinical Isolates Barat, Stephen Angulo, David Borroto-Esoda, Katyna Ghannoum, Mahmoud 2017 http://dx.doi.org/10.1093/ofid/ofx163.902 http://academic.oup.com/ofid/article-pdf/4/suppl_1/S368/33612578/ofx163.902.pdf en eng Oxford University Press (OUP) http://creativecommons.org/licenses/by-nc-nd/4.0 CC-BY-NC-ND Open Forum Infectious Diseases volume 4, issue suppl_1, page S368-S369 ISSN 2328-8957 Infectious Diseases Oncology journal-article 2017 croxfordunivpr https://doi.org/10.1093/ofid/ofx163.902 2022-04-15T06:30:29Z Abstract Background Global rates of candidemia caused by C. parapsilosis are increasing with differences detected between neonates and adult patients (50% vs. 12%, respectively) and across geographic regions (5% vs. 25% in Iceland and Spain, respectively). SCY-078 is a novel, oral and intravenous, triterpenoid glucan synthase inhibitor under development for the treatment of invasive candidiasis. This study evaluated the in vitro antifungal activity of SCY-078 against a collection of clinical C. parapsilosis isolates. Methods Retrospective analysis of data from 7 independent studies evaluating the activity of SCY-078 is presented. Data were available for 206 C. parapsilosis isolates collected between 2008 and 2015 in the US and EU. The collection included 186 wild-type isolates as well as 14 azole-resistant, and 6 echinocandin-resistant isolates. Minimum inhibitory concentrations (MIC) were determined according to the CLSI M27-A3 and EUCAST E.DEF 7.3 guidelines. Comparator compounds varied across studies and included fluconazole, micafungin (MCF), caspofungin (CSP), and anidulafungin (ANI). MIC50 and MIC90 values were defined as the concentrations inhibiting growth of 50% and 90% of isolates, respectively. Echinocandin and azole resistance were determined based on CLSI M27-A4 guidelines. Results The MIC50 values obtained for SCY-078 against the wild-type C. parapsilosis isolates across the 7 studies ranged from 0.25 to 1 μg/mL and the MIC90 values ranged from 0.25 -2 µg/mL. Among the echinocandins, MIC90 values ranged from 0.5 to 2 µg/mL (CSP), 1 to 4 µg/mL (MCF) and 2 to 4 µg/mL (ANI). SCY-078 was active against the 14 azole-resistant isolates (MIC ranging from 0.25 to 2 µg/mL). Similar activity was observed across the 6 echinocandin-resistant isolates with MIC values for SCY-078 ranging from 0.25 to 1 µg/mL. Among the 4 most recent studies in the US and EU (2013–2015) C. parapsilosis isolates represented 14 – 20% of the Candidaisolates; rates were similar in the EU and US. Conclusion SCY-078 demonstrated potent activity against C. parapsilosis clinical isolates. Notably, SCY-078 was effective against all the echinocandin and azole resistant C. parapsilosis isolates tested. Disclosures S. Barat, Scynexis, Inc: Employee, Salary; D. Angulo, Scynexis, Inc.: Employee, Salary; K. Borroto-Esoda, Scynexis Inc.: Consultant, Consulting fee; M. Ghannoum, Scynexis, Inc.: Consultant, Investigator and Scientific Advisor, Consulting fee, Research grant and Research support Article in Journal/Newspaper Iceland Oxford University Press (via Crossref) Open Forum Infectious Diseases 4 suppl_1 S368 S369
institution Open Polar
collection Oxford University Press (via Crossref)
op_collection_id croxfordunivpr
language English
topic Infectious Diseases
Oncology
spellingShingle Infectious Diseases
Oncology
Barat, Stephen
Angulo, David
Borroto-Esoda, Katyna
Ghannoum, Mahmoud
Assessment of the In Vitro Antifungal Activity of SCY-078 Against a Collection of C. parapsilosis Clinical Isolates
topic_facet Infectious Diseases
Oncology
description Abstract Background Global rates of candidemia caused by C. parapsilosis are increasing with differences detected between neonates and adult patients (50% vs. 12%, respectively) and across geographic regions (5% vs. 25% in Iceland and Spain, respectively). SCY-078 is a novel, oral and intravenous, triterpenoid glucan synthase inhibitor under development for the treatment of invasive candidiasis. This study evaluated the in vitro antifungal activity of SCY-078 against a collection of clinical C. parapsilosis isolates. Methods Retrospective analysis of data from 7 independent studies evaluating the activity of SCY-078 is presented. Data were available for 206 C. parapsilosis isolates collected between 2008 and 2015 in the US and EU. The collection included 186 wild-type isolates as well as 14 azole-resistant, and 6 echinocandin-resistant isolates. Minimum inhibitory concentrations (MIC) were determined according to the CLSI M27-A3 and EUCAST E.DEF 7.3 guidelines. Comparator compounds varied across studies and included fluconazole, micafungin (MCF), caspofungin (CSP), and anidulafungin (ANI). MIC50 and MIC90 values were defined as the concentrations inhibiting growth of 50% and 90% of isolates, respectively. Echinocandin and azole resistance were determined based on CLSI M27-A4 guidelines. Results The MIC50 values obtained for SCY-078 against the wild-type C. parapsilosis isolates across the 7 studies ranged from 0.25 to 1 μg/mL and the MIC90 values ranged from 0.25 -2 µg/mL. Among the echinocandins, MIC90 values ranged from 0.5 to 2 µg/mL (CSP), 1 to 4 µg/mL (MCF) and 2 to 4 µg/mL (ANI). SCY-078 was active against the 14 azole-resistant isolates (MIC ranging from 0.25 to 2 µg/mL). Similar activity was observed across the 6 echinocandin-resistant isolates with MIC values for SCY-078 ranging from 0.25 to 1 µg/mL. Among the 4 most recent studies in the US and EU (2013–2015) C. parapsilosis isolates represented 14 – 20% of the Candidaisolates; rates were similar in the EU and US. Conclusion SCY-078 demonstrated potent activity against C. parapsilosis clinical isolates. Notably, SCY-078 was effective against all the echinocandin and azole resistant C. parapsilosis isolates tested. Disclosures S. Barat, Scynexis, Inc: Employee, Salary; D. Angulo, Scynexis, Inc.: Employee, Salary; K. Borroto-Esoda, Scynexis Inc.: Consultant, Consulting fee; M. Ghannoum, Scynexis, Inc.: Consultant, Investigator and Scientific Advisor, Consulting fee, Research grant and Research support
format Article in Journal/Newspaper
author Barat, Stephen
Angulo, David
Borroto-Esoda, Katyna
Ghannoum, Mahmoud
author_facet Barat, Stephen
Angulo, David
Borroto-Esoda, Katyna
Ghannoum, Mahmoud
author_sort Barat, Stephen
title Assessment of the In Vitro Antifungal Activity of SCY-078 Against a Collection of C. parapsilosis Clinical Isolates
title_short Assessment of the In Vitro Antifungal Activity of SCY-078 Against a Collection of C. parapsilosis Clinical Isolates
title_full Assessment of the In Vitro Antifungal Activity of SCY-078 Against a Collection of C. parapsilosis Clinical Isolates
title_fullStr Assessment of the In Vitro Antifungal Activity of SCY-078 Against a Collection of C. parapsilosis Clinical Isolates
title_full_unstemmed Assessment of the In Vitro Antifungal Activity of SCY-078 Against a Collection of C. parapsilosis Clinical Isolates
title_sort assessment of the in vitro antifungal activity of scy-078 against a collection of c. parapsilosis clinical isolates
publisher Oxford University Press (OUP)
publishDate 2017
url http://dx.doi.org/10.1093/ofid/ofx163.902
http://academic.oup.com/ofid/article-pdf/4/suppl_1/S368/33612578/ofx163.902.pdf
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op_source Open Forum Infectious Diseases
volume 4, issue suppl_1, page S368-S369
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op_doi https://doi.org/10.1093/ofid/ofx163.902
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