Hepatitis B In Silico Trials Capture Functional Cure, Indicate Mechanistic Pathways, and Suggest Prognostic Biomarker Signatures.

Journal: Clinical pharmacology and therapeutics
Published Date:

Abstract

In silico trials, utilizing mathematical models calibrated with clinical data, present a transformative approach to expedite drug development. We propose a virtual trial framework for chronic Hepatitis B, accurately simulating clinical protocols, patient characteristics, and endpoints using a mechanistic mathematical model. Clinical trial simulations with this model successfully captured functional cure with standard-of-care therapies (nucleos(t)ide analogs and pegylated interferon) as well as complex clinical observations, facilitating mechanistic hypothesis generation and suggesting biomarker signatures that may predict treatment outcomes. In silico trials revealed that responders exhibited enhanced cytotoxic immunity and significant serum-alanine transaminase increases, suggesting a potential response biomarker. However, a higher baseline Hepatitis B surface antigen did not proportionately increase cytotoxic antiviral immune responses, indicating a potential immune ceiling but in the face of increasing systemic antigen burden, therefore culminating in a lower treatment response. Virtual patients enabled the generation of large virology biomarker synthetic datasets, which empowered a machine learning model to predict functional cure in virtual patients with ~ 95% accuracy. This underscores the potential of in silico trials in enhancing clinical trials, generating mechanistic hypotheses, and accelerating chronic Hepatitis B drug development.

Authors

  • Javiera Cortés-Ríos
    Department of Pharmaceutical Sciences, School of Pharmacy and Pharmaceutical Sciences, State University of New York at Buffalo, USA.
  • Tianjing Ren
    Department of Pharmaceutical Sciences, School of Pharmacy and Pharmaceutical Sciences, State University of New York at Buffalo, USA.
  • Nathan Hanan
    Clinical Pharmacology Modelling & Simulation, GSK, Collegeville, Pennsylvania, USA.
  • Anna Sher
    Clinical Pharmacology Modelling & Simulation, GSK, Waltham, MA, USA.
  • Ahmed Nader
    Clinical Pharmacology Modelling & Simulation, GSK, Collegeville, Pennsylvania, USA.
  • Mindy Magee
    GlaxoSmithKline, Upper Providence, PA, USA.
  • William J Jusko
    Department of Pharmaceutical Sciences, School of Pharmacy and Pharmaceutical Sciences, State University of New York at Buffalo, USA.
  • Rajat Desikan
    Clinical Pharmacology Modelling & Simulation, GSK, Collegeville, Pennsylvania, USA.

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