A Call to Action for New Global Approaches to Cardiovascular Disease Drug Solutions

Author:

Figtree Gemma A.1ORCID,Broadfoot Keith2,Casadei Barbara345ORCID,Califf Robert6ORCID,Crea Filippo7ORCID,Drummond Grant R.8ORCID,Freedman Jane E.9ORCID,Guzik Tomasz J.1011,Harrison David12,Hausenloy Derek J.1314151617,Hill Joseph A.18ORCID,Januzzi James L.19,Kingwell Bronwyn A.20ORCID,Lam Carolyn S.P.21,MacRae Calum A.22,Misselwitz Frank23ORCID,Miura Tetsuji24ORCID,Ritchie Rebecca H.25ORCID,Tomaszewski Maciej26ORCID,Wu Joseph C.27ORCID,Xiao Junjie28,Zannad Faiez29ORCID

Affiliation:

1. Kolling Institute, Royal North Shore Hospital, University of Sydney, Australia (G.A.F.).

2. Clinical Committee, National Heart Foundation of Australia (K.B.).

3. Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, UK (B.C.).

4. NIHR Oxford Biomedical Research Centre, UK (B.C.).

5. British Heart Foundation Centre of Research Excellence, Oxford, UK (B.C.).

6. Verily, South San Francisco, CA (R.C.).

7. Catholic University, Rome, Italy (F.C.).

8. Centre for Cardiovascular Biology and Disease Research and Department of Physiology, Anatomy and Microbiology, La Trobe University, Melbourne, Australia (G.R.D.).

9. Cardiovascular Research, University of Massachusetts Medical School, Worcester (J.E.F.).

10. Institute of Cardiovascular and Medical Sciences, University of Glasgow, UK (T.J.G.).

11. Jagiellonian University Collegium Medicum, Krakow, Poland (T.J.G.).

12. Clinical Pharmacology, Vanderbilt University School of Medicine, Nashville, TN (D.H.).

13. Signature Research Program in Cardiovascular & Metabolic Disorders Program, Duke–National University of Singapore NUS Medical School (D.J.H.).

14. National Heart Research Institute Singapore, National Heart Centre (D.J.H.).

15. Yong Loo Lin School of Medicine, National University Singapore (D.J.H.).

16. The Hatter Cardiovascular Institute, University College London, UK (D.J.H.).

17. Cardiovascular Research Center, College of Medical and Health Sciences, Asia University, Taiwan (D.J.H.).

18. University of Texas Southwestern, Dallas (J.A.H.).

19. Massachusetts General Hospital, Harvard University, Boston (J.L.J.).

20. CSL Ltd, Melbourne, Australia (B.A.K.).

21. National Heart Centre Singapore and Duke–National University of Singapore (C.S.P.L.).

22. Brigham and Women’s Hospital, Harvard Medical School, Boston, MA (C.A.M.).

23. Bayer AG, Pharmaceuticals Division, Wuppertal, Germany (F.M.).

24. Department of Cardiovascular, Renal and Metabolic Medicine, Sapporo Medical University, Japan (T.M.).

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

26. Division of Cardiovascular Sciences, Faculty of Biology, Medicine and Health and Manchester University NHS Foundation Trust, University of Manchester, UK (M.T.).

27. Stanford Cardiovascular Institute, CA (J.C.W.).

28. Cardiac Regeneration and Ageing Laboratory, Institute of Cardiovascular Sciences, School of Life Sciences, Shanghai University, China (J.X.).

29. Universite´ de Lorraine, INSERM CIC 1493, INI CRCT, CHRU, Nancy, France (F.Z.).

Abstract

While 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.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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