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

Author:

Figtree Gemma A1ORCID,Broadfoot Keith2,Casadei Barbara345ORCID,Califf Robert6ORCID,Crea Filippo7ORCID,Drummond Grant R8ORCID,Freedman Jane E9ORCID,Guzik Tomasz J10,Harrison David11,Hausenloy Derek J1213141516,Hill Joseph A17ORCID,Januzzi James L18,Kingwell Bronwyn A19ORCID,Lam Carolyn S P20,MacRae Calum A21,Misselwitz Frank22ORCID,Miura Tetsuji23ORCID,Ritchie Rebecca H24ORCID,Tomaszewski Maciej25ORCID,Wu Joseph C26ORCID,Xiao Junjie27,Zannad Faiez28ORCID

Affiliation:

1. Kolling Institute, Royal North Shore Hospital, University of Sydney, Sydney, Australia

2. Clinical Committee, National Heart Foundation of Australia

3. Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK

4. NIHR Oxford Biomedical Research Centre, Oxford, UK

5. British Heart Foundation Centre of Research Excellence, Oxford, UK

6. Verily

7. Catholic University, Roma, Italy

8. Centre for Cardiovascular Biology and Disease Research; and Department of Physiology, Anatomy and Microbiology, La Trobe University, Melbourne, Australia

9. Cardiovascular Research, University of Massachusetts Medical School, MA, USA

10. Institute of Cardiovascular and Medical Sciences, University of Glasgow, UK and Jagiellonian University Collegium Medicum, Krakow, Poland

11. Clinical Pharmacology, Vanderbilt University School of Medicine, Nashville, TN, USA

12. Signature Research Program in Cardiovascular & Metabolic Disorders Program, Duke-National University of Singapore NUS Medical School, Singapore

13. National Heart Research Institute Singapore, National Heart Centre, Singapore

14. Yong Loo Lin School of Medicine, National University Singapore, Singapore

15. The Hatter Cardiovascular Institute, University College London, London, UK

16. Cardiovascular Research Center, College of Medical and Health Sciences, Asia University, Taiwan

17. University of Texas Southwestern, Dallas, TX, USA

18. Massachusetts General Hospital, Harvard University, Boston, MA, USA

19. CSL Limited, Melbourne, Australia

20. National Heart Centre Singapore and Duke-National University of Singapore

21. Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, USA

22. Bayer AG, Pharmaceuticals Division, Wuppertal, Germany

23. Department of Cardiovascular, Renal and Metabolic Medicine, Sapporo Medical University, Sapporo, Japan

24. Drug Discovery Biology, Monash Institute of Pharmaceutical Sciences, Monash University (Parkville Campus), Parkville, VIC, Australia

25. Division of Cardiovascular Sciences, Faculty of Biology, Medicine and Health and Manchester University NHS Foundation Trust, University of Manchester, Manchester, UK

26. Stanford Cardiovascular Institute, Stanford, CA, USA

27. Cardiac Regeneration and Ageing Lab, Institute of Cardiovascular Sciences, School of Life Sciences, Shanghai University, Shanghai, 200444, China

28. Université de Lorraine, INSERM CIC 1493, INI CRCT, CHRU Nancy, France

Abstract

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.

Funder

National Health and Medical Research Council

Biomarkers and Oxidative Stress awarded USA

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

Reference55 articles.

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