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EDP-938, a novel nucleoprotein inhibitor of respiratory syncytial virus,demonstrates potent antiviral activities in vitro and in a non-human primate model
Authors:Michael H. J. Rhodin  Nicole V. McAllister  Jonathan Castillo  Sarah L. Noton  Rachel Fearns  In Jong Kim  Jianming Yu  Thomas P. Blaisdell  Joseph Panarese  Brian C. Shook  Yat Sun Or  Bryan Goodwin  Kai Lin
Affiliation:1. Enanta Pharmaceuticals Inc., Watertown, Massachusetts, United States of America;2. Department of Microbiology, Boston University School of Medicine, Boston, Massachusetts, United States of America;ViiV Healthcare, UNITED STATES
Abstract:EDP-938 is a novel non-fusion replication inhibitor of respiratory syncytial virus (RSV). It is highly active against all RSV-A and B laboratory strains and clinical isolates tested in vitro in various cell lines and assays, with half-maximal effective concentrations (EC50s) of 21, 23 and 64 nM against Long (A), M37 (A) and VR-955 (B) strains, respectively, in the primary human bronchial epithelial cells (HBECs). EDP-938 inhibits RSV at a post-entry replication step of the viral life cycle as confirmed by time-of-addition study, and the activity appears to be mediated by viral nucleoprotein (N). In vitro resistance studies suggest that EDP-938 presents a higher barrier to resistance compared to viral fusion or non-nucleoside L polymerase inhibitors with no cross-resistance observed. Combinations of EDP-938 with other classes of RSV inhibitors lead to synergistic antiviral activity in vitro. Finally, EDP-938 has also been shown to be efficacious in vivo in a non-human primate model of RSV infection.
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