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.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 1019-1036 |
| Number of pages | 18 |
| Journal | Facets |
| Volume | 5 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 17 Dec 2021 |
| Externally published | Yes |
Keywords
- COVID-19
- Drug discovery
- Intellectual property rights
- Market failure
- Open science
- Pandemic preparedness
- Public private partnerships
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