Medicine for Tomorrow: Some Alternative Proposals to Promote Socially Beneficial Research and Development in Pharmaceuticals

@article{Stiglitz2010MedicineFT,
  title={Medicine for Tomorrow: Some Alternative Proposals to Promote Socially Beneficial Research and Development in Pharmaceuticals},
  author={J. E. Stiglitz and Arjun Jayadev},
  journal={Journal of Generic Medicines: The Business Journal for the Generic Medicines Sector},
  year={2010},
  volume={7},
  pages={217 - 226}
}
  • J. StiglitzArjun Jayadev
  • Published 1 July 2010
  • Political Science
  • Journal of Generic Medicines: The Business Journal for the Generic Medicines Sector
The current models of pharmaceutical drug discovery display significant inefficiencies. One inefficiency is the widespread prevalence of me-too drugs. Second, some patents can act as barriers to knowledge, by slowing down the pace of new discoveries. Third, there are higher costs for the public, who end up paying double costs — subsidizing or funding research and development (R & D) that leads to new discoveries on the one hand, and, on the other, paying the social costs of restricted access to… 

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References

SHOWING 1-10 OF 29 REFERENCES

The Benefits and Savings from Publicly Funded Clinical Trials of Prescription Drugs

  • D. Baker
  • Medicine, Political Science
    International journal of health services : planning, administration, evaluation
  • 2008
A system of publicly financed clinical trials under which all results are fully available to the public is outlined, financed by paying lower drug prices under the Medicare drug program and other public health care programs.

Two ideas to increase innovation and reduce pharmaceutical costs and prices.

This Perspective reviews two policies that could assist in realigning incentives toward genuine innovation while also keeping drug spending growth under check.

Paying for Delay: Pharmaceutical Patent Settlement as a Regulatory Design Problem

Over the past decade, drug makers have settled patent litigation by making large payments to potential rivals who, in turn, abandon suits that (if successful) would increase competition. Because such

The Health Impact Fund: A Useful Supplement to the Patent System?

The Health Impact Fund has been proposed as an optional, comprehensive advance market commitment system offering financial payments or ‘prizes’ to patentees of new drugs, which are sold globally at

Beware Those Bearing Gifts: Physicians' Fiduciary Duty to Avoid Pharmaceutical Marketing

The physicians’ fiduciary duty to their patients is used as a means to further encourage physicians to refrain from inappropriately accepting gifts from agents of pharmaceutical companies seeking to market their products and to ensure that the well-being of their patients remains their focus.

Prescription drug spending trends in the United States: looking beyond the turning point.

Trends are documented and underlying components are identified: declines in the role of blockbuster drugs, increased importance of biologics and vaccines relative to traditional pharmaceuticals, and a changing medication mix away from those prescribed principally by primary care physicians toward those mostly prescribed by specialists.

The Case for Public Funding and Public Oversight of Clinical Trials

Clinical drug trials are public goods and should be publicly funded to avoid undersupply, the suppression of adverse results and other problems, according to Tracy R. Lewis, Jerome H. Reichman and

Pharmaceutical expenditure, total health-care expenditure and GDP.

It is concluded that the changes in the elasticity of pharmaceutical expenditure and in the Total HCE elasticity are due to the private component and the pharmaceutical expenditure behaviour, respectively.

Antitrust Limits to Patent Settlements

This paper focuses on the class of legal rules that governs intellectual property rights: the antitrust limits imposed on patent settlements. The paper discusses the benefits and costs of settlements