Preclinical Profile of AB-423, an Inhibitor of Hepatitis B Virus Pregenomic RNA Encapsidation

Author:

Mani Nagraj1ORCID,Cole Andrew G.1,Phelps Janet R.1,Ardzinski Andrzej1,Cobarrubias Kyle D.1,Cuconati Andrea1,Dorsey Bruce D.1,Evangelista Ellen1,Fan Kristi1,Guo Fang1,Guo Haitao2,Guo Ju-Tao3,Harasym Troy O.1,Kadhim Salam1,Kultgen Steven G.1,Lee Amy C. H.1,Li Alice H. L.1,Long Quanxin2,Majeski Sara A.1,Mao Richeng2,McClintock Kevin D.1,Reid Stephen P.1,Rijnbrand Rene1,Snead Nicholas M.1,Micolochick Steuer Holly M.1,Stever Kim1,Tang Sunny1,Wang Xiaohe1,Zhao Qiong3,Sofia Michael J.1

Affiliation:

1. Arbutus Biopharma Inc., Warminster, Pennsylvania, USA, and Burnaby, British Columbia, Canada

2. Indiana University, Indianapolis, Indiana, USA

3. Baruch S. Blumberg Institute, Doylestown, Pennsylvania, USA

Abstract

ABSTRACT AB-423 is a member of the sulfamoylbenzamide (SBA) class of hepatitis B virus (HBV) capsid inhibitors in phase 1 clinical trials. In cell culture models, AB-423 showed potent inhibition of HBV replication (50% effective concentration [EC 50 ] = 0.08 to 0.27 μM; EC 90 = 0.33 to 1.32 μM) with no significant cytotoxicity (50% cytotoxic concentration > 10 μM). Addition of 40% human serum resulted in a 5-fold increase in the EC 50 s. AB-423 inhibited HBV genotypes A through D and nucleos(t)ide-resistant variants in vitro . Treatment of HepDES19 cells with AB-423 resulted in capsid particles devoid of encapsidated pregenomic RNA and relaxed circular DNA (rcDNA), indicating that it is a class II capsid inhibitor. In a de novo infection model, AB-423 prevented the conversion of encapsidated rcDNA to covalently closed circular DNA, presumably by interfering with the capsid uncoating process. Molecular docking of AB-423 into crystal structures of heteroaryldihydropyrimidines and an SBA and biochemical studies suggest that AB-423 likely also binds to the dimer-dimer interface of core protein. In vitro dual combination studies with AB-423 and anti-HBV agents, such as nucleos(t)ide analogs, RNA interference agents, or interferon alpha, resulted in additive to synergistic antiviral activity. Pharmacokinetic studies with AB-423 in CD-1 mice showed significant systemic exposures and higher levels of accumulation in the liver. A 7-day twice-daily administration of AB-423 in a hydrodynamic injection mouse model of HBV infection resulted in a dose-dependent reduction in serum HBV DNA levels, and combination with entecavir or ARB-1467 resulted in a trend toward antiviral activity greater than that of either agent alone, consistent with the results of the in vitro combination studies. The overall preclinical profile of AB-423 supports its further evaluation for safety, pharmacokinetics, and antiviral activity in patients with chronic hepatitis B.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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