Susceptibility of Herpes Simplex Virus Isolated from Genital Herpes Lesions to ASP2151, a Novel Helicase-Primase Inhibitor

Author:

Katsumata Kiyomitsu1,Weinberg Adriana2,Chono Koji1,Takakura Shoji1,Kontani Toru1,Suzuki Hiroshi1

Affiliation:

1. Department of Drug Discovery Research, Astellas Pharma Inc., Tsukuba, Ibaraki, Japan

2. University of Colorado Hospital and Departments of Pediatrics, Medicine and Pathology, University of Colorado, Denver, Aurora, Colorado, USA

Abstract

ABSTRACT ASP2151 (amenamevir) is a helicase-primase inhibitor against herpes simplex virus type 1 (HSV-1), HSV-2, and varicella-zoster virus. To evaluate the anti-HSV activity of ASP2151, susceptibility testing was performed on viruses isolated from patients participating in a placebo- and valacyclovir-controlled proof-of-concept phase II study for recurrent genital herpes. A total of 156 HSV strains were isolated prior to the dosing of patients, and no preexisting variants with less susceptibility to ASP2151 or acyclovir (ACV) were detected. ASP2151 inhibited HSV-1 and HSV-2 replication with mean 50% effective concentrations (EC 50 s) of 0.043 and 0.069 μM, whereas ACV exhibited mean EC 50 s of 2.1 and 3.2 μM, respectively. Notably, the susceptibilities of HSV isolates to ASP2151 and ACV were not altered after dosing with the antiviral agents. Taken together, these results demonstrate that ASP2151 inhibits the replication of HSV clinical isolates more potently than ACV, and HSV resistant to this novel helicase-primase inhibitor as well as ACV may not easily emerge in short-term treatment for recurrent genital herpes patients.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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