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Abstract
Science has made remarkable advances in understanding the molecular basis of disease, generating new and effective rationally-designed treatments at an accelerating rate. Ironically, the successes of science is creating a crisis in the affordability of equitable health care. The COVID-19 pandemic underscores both the value of science in health care, and the apparently inevitable tension between health and the economy. Drug development in ever-smaller target populations is a critical component of the rising costs of care. For structural and historical reasons, drug development is inefficient and poorly integrated across the public and private sectors. We postulate an alternative, integrated model in which governments and industry share the risks and benefits of drug development. The Australian government recently announced support for a AU$185 million innovative multi-stakeholder public-private partnership model for sustainable precision oncology, accelerating biomarker-dependent drug development through integrating clinical trials into the standard of care.
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Details

1 Harvard Medical School and Harvard Pilgrim Health Care Institute, Department of Population Medicine, Boston, USA (GRID:grid.38142.3c) (ISNI:000000041936754X)
2 Omico: Australian Geneomic Cancer Medicine Centre Ltd, Darlinghurst, Australia (GRID:grid.38142.3c)
3 UNSW, Genomic Cancer Medicine Laboratory, Garvan Institute of Medical Research, Omico: Australian Genomic Cancer Medicine Centre Ltd, St Vincent’s Clinical School, Faculty of Medicine, Sydney, Australia (GRID:grid.1005.4) (ISNI:0000 0004 4902 0432)