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Full Description
This study develops a detailed description of the successful technology transfer of an invention — the drug-eluting coronary stent — originating in intramural research within the US National Institutes of Health. The history of the commercialization of the invention is used to illustrate a new policy, proposed and explained in this study, for the payment to the government of royalties on the sales of biomedical products developed with substantial public funding provided through indirect as well as direct funding avenues. The proposed policy addresses concerns about the high prices that taxpayers as consumers pay for biomedical products that were developed with funding from the taxpayers as investors. The study explains the theoretical circumstances in which the policy would not adversely affect the appropriate level of R&D investment, and then uses the history of the drug-eluting coronary stent as an example where biomedical R&D is consistent with those circumstances.
Contents
1. Introduction
2. The Two Avenues for Public Funding of Pharmaceutical and Other Biomedical R&D
3. The Story of Drug-Eluting Coronary Stents
4. The Incentives Issue
5. The Circumstances Affecting Incentives for the Development of Drug-Eluting Stents
6. A Proposal for Government Royalties for Biomedical Products Developed with Substantial Public Funding for R&D
7. Conclusion
Acknowledgements
Appendices
A. Incomplete Pass Through of the Royalty to Price Given Market Power
About the Authors
References



