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Comparative Effectiveness, Personalized Medicine and Innovation

The Path Forward

  • Industry Perspectives
  • Comparative Effectiveness and Personalized Medicine
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Notes

  1. For patients, avoidance of unnecessary or unbeneficial therapies offers potentially far-reaching benefits, including avoidance of long-term complications and the worsening of a health condition or overall health.

  2. Although the possibility exists for faster and less expensive phase III trials, with reduced required trial sizes for personalized therapies for which biomarkers and/or companion diagnostics might be available, on the whole — and especially in early stages — development costs and timelines could actually increase.[6]

  3. The Genetic Information Nondiscrimination Act of 2008[9] is a newly implemented federal law that aims to protect individuals from being treated unfairly because of differences in their DNA that may affect their health. The law prevents discrimination from health insurers and employers. The law was crafted with the intent to help ease concerns about discrimination that might keep some people from getting genetic tests that could benefit their health. The law also enables people to take part in research studies without fear that their DNA information might be used against them in terms of their health insurance or in the workplace.

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Acknowledgements

The authors are all employees of, and shareholders in, Johnson & Johnson.

No external sources of funding were used to assist in the preparation of this article.

The authors extend a special thank you to Jami Taylor for her invaluable assistance in research and in the preparation of this manuscript.

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Thomas, A., Phillips, A., Donnelly, R. et al. Comparative Effectiveness, Personalized Medicine and Innovation. Pharmacoeconomics 28, 923–930 (2010). https://doi.org/10.2165/11539030-000000000-0000010.2165/11537370-000000000-00000

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