1. Academic Validation
  2. SB 9200, a novel agonist of innate immunity, shows potent antiviral activity against resistant HCV variants

SB 9200, a novel agonist of innate immunity, shows potent antiviral activity against resistant HCV variants

  • J Med Virol. 2017 Sep;89(9):1620-1628. doi: 10.1002/jmv.24809.
Meleri Jones 1 Morven E Cunningham 1 Peter Wing 1 Sampath DeSilva 1 Rupa Challa 2 Anjaneyulu Sheri 2 Seetharamaiyer Padmanabhan 2 Radhakrishnan P Iyer 2 Brent E Korba 3 Nezam Afdhal 3 Graham R Foster 1
Affiliations

Affiliations

  • 1 The Liver Unit, Blizard Institute, Barts Health, Queen Mary University of London, London, UK.
  • 2 Spring Bank Pharmaceuticals, Milford, Massachusetts.
  • 3 Department of Microbiology & Immunology, Georgetown University Medical Centre, Washington, District of Columbia.
Abstract

SB 9200 is a novel, first-in-class oral modulator of innate immunity that is believed to act via the activation of the RIG-I and NOD2 pathways. SB 9200 has broad-spectrum Antiviral activity against RNA viruses including hepatitis C virus (HCV), norovirus, respiratory syncytial virus, and influenza and has demonstrated activity against hepatitis B virus (HBV) in vitro and in vivo. In phase I clinical trials in chronically infected HCV patients, SB 9200 has been shown to reduce HCV RNA by up to 1.9 log10 . Here, we demonstrate the Antiviral activity of SB 9200 against a HCV replicon system and patient derived virus. Using the HCV capture-fusion assay, we show that SB 9200 is active against diverse HCV genotypes and is also effective against HCV derived from patients who relapse following direct-acting Antiviral treatment, including viruses containing known NS5A resistance-associated sequences. These data confirm the broad Antiviral activity of SB 9200 and indicate that it may have clinical utility in HCV patients who have failed to respond to current Antiviral regimens.

Keywords

antiviral agents; disease control, anti-hepatitis C virus DAA (directly acting antivirals); hepatitis C virus; virus classification, antiviral agents.

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