Open drug discovery of anti-virals critical for Canada’s pandemic strategy

Author:

Bubela Tania1,Gold E. Richard2,Goel Vivek3,Morgan Max45,Mossman Karen6,Nickerson Jason78,Patrick David910,Edwards Aled1112

Affiliation:

1. Faculty of Health Sciences, Simon Fraser University, Burnaby, BC V5A 1S6, Canada

2. Faculty of Law, McGill University, Montreal, QC H3A 1W9, Canada

3. Institute of Health Policy, Management and Evaluation, Dalla Lana School of Public Health, University of Toronto, Toronto, ON M5T 3M6, Canada

4. M4K Pharma, Inc., Toronto, ON M5G 1L7, Canada

5. Structural Genomics Consortium (SGC), Toronto, ON M5G 1L7, Canada

6. Pathology and Molecular Medicine, McMaster Immunology Research Centre, McMaster University, Hamilton, ON L8S 4L8, Canada

7. University of Ottawa, Ottawa, ON K1N 6K5, Canada

8. Bruyère Research Institute, Ottawa, ON K1N 5C8, Canada

9. British Columbia Centre for Disease Control, Vancouver, BC V5Z 4R4, Canada

10. School of Population and Public Health, University of British Columbia, Vancouver, BC V6T 1Z3, Canada

11. Molecular Genetics and Medical Biophysics, University of Toronto, Toronto, ON M5G 1L5, Canada

12. SGC, London, UK

Abstract

In the event of the current COVID-19 pandemic and in preparation for future pandemics, open science can support mission-oriented research and development, as well as commercialization. Open science shares skills and resources across sectors; avoids duplication and provides the basis for rapid and effective validation due to full transparency. It is a strategy that can adjust quickly to reflect changing incentives and priorities, because it does not rely on any one actor or sector. While eschewing patents, it can ensure high-quality drugs, low pricing, and access through existing regulatory mechanisms. Open science practices and partnerships decrease transaction costs, increase diversity of actors, reduce overall costs, open new, higher-risk/higher-impact approaches to research, and provide entrepreneurs freedom to operate and freedom to innovate. We argue that it is time to re-open science, not only in its now restricted arena of fundamental research, but throughout clinical translation. Our model and attendant recommendations map onto a strategy to accelerate discovery of novel broad-spectrum anti-viral drugs and clinical trials of those drugs, from first-in-human safety-focused trials to late stage trials for efficacy. The goal is to ensure low-cost and rapid access, globally, and to ensure that Canadians do not pay a premium for drugs developed from Canadian science.

Publisher

Canadian Science Publishing

Subject

Multidisciplinary

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