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A call to action for new global approaches to cardiovascular disease drug solutions

  • Gemma A Figtree
  • , Keith Broadfoot
  • , Barbara Casadei
  • , Robert Califf
  • , Filippo Crea
  • , Grant R Drummond
  • , Jane E Freedman
  • , Tomasz J Guzik
  • , David Harrison
  • , Derek J Hausenloy
  • , Joseph A Hill
  • , James L Januzzi
  • , Bronwyn A Kingwell
  • , Carolyn S P Lam
  • , Calum A MacRae
  • , Frank Misselwitz
  • , Tetsuji Miura
  • , Rebecca H Ritchie
  • , Maciej Tomaszewski
  • , Joseph C Wu
  • Junjie Xiao, Faiez Zannad
  • Western Sydney University
  • National Heart Foundation of Australia
  • Oxford University
  • Verily Life Sciences
  • Lyon Catholic University
  • La Trobe University
  • University of Massachusetts Medical School
  • University Court of the University of Glasgow
  • Duke-NUS Medical School
  • University of Texas Southwestern Medical Centre, Dallas
  • Harvard University
  • CSL Limited
  • National University Heart Centre
  • Harvard Medical School
  • Bayer CropScience AG
  • Sapporo Medical University
  • Monash University
  • Stanford University Medical Center
  • Shanghai Jiao Tong University
  • Université de Lorraine
  • National University of Singapore (NUS)

Research output: Contribution to journalArticlepeer-review

Abstract

Whilst we continue to wrestle with the immense challenge of implementing equitable access to established evidence-based treatments, substantial gaps remain in our pharmacotherapy armament for common forms of cardiovascular disease including coronary and peripheral arterial disease, heart failure, hypertension, and arrhythmia. We need to continue to invest in the development of new approaches for the discovery, rigorous assessment, and implementation of new therapies. Currently, the time and cost to progress from lead compound/product identification to the clinic, and the success rate in getting there reduces the incentive for industry to invest, despite the enormous burden of disease and potential size of market. There are tremendous opportunities with improved phenotyping of patients currently batched together in syndromic 'buckets'. Use of advanced imaging and molecular markers may allow stratification of patients in a manner more aligned to biological mechanisms that can, in turn, be targeted by specific approaches developed using high-throughput molecular technologies. Unbiased 'omic' approaches enhance the possibility of discovering completely new mechanisms in such groups. Furthermore, advances in drug discovery platforms, and models to study efficacy and toxicity more relevant to the human disease, are valuable. Re-imagining the relationships among discovery, translation, evaluation, and implementation will help reverse the trend away from investment in the cardiovascular space, establishing innovative platforms and approaches across the full spectrum of therapeutic development.

Original languageEnglish
Pages (from-to)1464-1475
Number of pages12
JournalEuropean Heart Journal
Volume42
Issue number15
DOIs
Publication statusPublished - 14 Apr 2021

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being
  2. SDG 9 - Industry, Innovation, and Infrastructure
    SDG 9 Industry, Innovation, and Infrastructure

Keywords

  • Atherosclerosis
  • Cardiovascular
  • Drug discovery
  • Heart failure
  • Multi-omics
  • Organoids
  • Pharmacotherapy
  • Precision medicine
  • Therapeutic target

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