Challenges and opportunities in drug development for nonalcoholic steatohepatitis

Eur J Pharmacol. 2020 Mar 5:870:172913. doi: 10.1016/j.ejphar.2020.172913. Epub 2020 Jan 10.

Abstract

Nonalcoholic fatty liver disease (NAFLD) and nonalcoholic steatohepatitis (NASH) are considered major global medical burdens with high prevalence and steeply rising incidence. Despite the characterization of numerous pathophysiologic pathways leading to metabolic disorder, lipid accumulation, inflammation, fibrosis, and ultimately end-stage liver disease or liver cancer formation, so far no causal pharmacological therapy is available. Drug development for NAFLD and NASH is limited by long disease duration and slow progression and the need for sequential biopsies to monitor the disease stage. Additional non-invasive biomarkers could therefore improve design and feasibility of such. Here, the current concepts on preclinical models, biomarkers and clinical endpoints and trial designs are briefly reviewed.

Keywords: Biomarker; Clinical trials; Drug development; Drug discovery; Nonalcoholic fatty liver disease (NAFLD); Nonalcoholic steatohepatitis (NASH).

Publication types

  • Review

MeSH terms

  • Animals
  • Biomarkers
  • Disease Progression
  • Drug Development
  • Fibrosis / complications
  • Fibrosis / drug therapy
  • Humans
  • Incidence
  • Inflammation / complications
  • Inflammation / drug therapy
  • Liver / metabolism
  • Liver Neoplasms / complications
  • Liver Neoplasms / drug therapy
  • Metabolic Diseases / complications
  • Metabolic Diseases / drug therapy
  • Non-alcoholic Fatty Liver Disease / drug therapy*
  • Non-alcoholic Fatty Liver Disease / metabolism*
  • Prevalence
  • Severity of Illness Index
  • Treatment Outcome

Substances

  • Biomarkers