Combination Therapy with Ibrexafungerp (Formerly SCY-078), a First-in-Class Triterpenoid Inhibitor of (1→3)-β- d -Glucan Synthesis, and Isavuconazole for Treatment of Experimental Invasive Pulmonary Aspergillosis

Author:

Petraitis Vidmantas1,Petraitiene Ruta1,Katragkou Aspasia2,Maung Bo Bo Win1,Naing Ethan1,Kavaliauskas Povilas1,Barat Stephen3,Borroto-Esoda Katyna3,Azie Nkechi3,Angulo David3,Walsh Thomas J.145

Affiliation:

1. Transplantation-Oncology Infectious Diseases Program, Division of Infectious Diseases, Department of Medicine, Weill Cornell Medicine of Cornell University, New York, New York, USA

2. Pediatric Infectious Disease Department, Nationwide Children’s Hospital, The Ohio State University, Columbus, Ohio, USA

3. Scynexis, Inc., Jersey City, New Jersey, USA

4. Department of Pediatrics, Weill Cornell Medicine, New York, New York, USA

5. Department of Microbiology and Immunology, Weill Cornell Medicine, New York, New York, USA

Abstract

Ibrexafungerp (formerly SCY-078) is a semisynthetic triterpenoid and potent (1→3)-β- d -glucan synthase inhibitor. We investigated the in vitro activity, pharmacokinetics, and in vivo efficacy of ibrexafungerp (SCY) alone and in combination with antimold triazole isavuconazole (ISA) against invasive pulmonary aspergillosis (IPA). The combination of ibrexafungerp and isavuconazole in in vitro studies resulted in additive and synergistic interactions against Aspergillus spp.

Funder

Scynexis, Inc.

Save Our Sick Kids Foundation

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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