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Data Exclusivity Periods and Pharmaceutical Innovation Print E-mail
SciMed - Healthcare
TS-Si News Service   
Monday, 10 January 2011 16:00
Los Angeles, CA, USA. A new study finds that extending the term of exclusive access will lead to higher drug costs in the short term, but also to more than 200 extra drug approvals and to greater life expectancy in the next several decades. The study published in Health Affairs is the first to estimate the financial and social impact of extending exclusive access to clinical trial data for conventional drugs.

Pharmaceutical companies and generic drug manufacturers have long been at odds over regulations about data exclusivity, the period of time before generic manufacturers can make use of valuable clinical trial data.

The pharmaceutical companies that introduce new drugs are currently granted five years of exclusive access to the clinical trial data they submit during the approval process. An extension of three years is available if new applications arise and a six month extension is granted if the drug is approved for use in pediatric populations.



Dana Goldman
Health Policy and Economics
University of Southern California (USC)
"Elected officials are unlikely to embrace legislation that would result in higher drug prices, but our research suggests that legislation to extend data exclusivity would spur innovation that would benefit future generations," says Dana Goldman, lead author, director of the Schaeffer Center for Health Policy and Economics at USC and the Chair in Medicine and Public Policy.

In 2007, the National Academies Committee on Science, Engineering and Public Policy called for extending the data exclusivity term to the longer period used in Europe, ten to 11 years. But generic manufacturers have argued for shorter limits so that they can bring less expensive versions of drugs to patients sooner.

"Unfortunately, the health policy literature contains no information about the effects such a policy would have on innovation, population longevity and social welfare," said Darius Lakdawalla, research director at the Schaeffer Center and associate professor in the USC School of Policy, Planning and Development.

The researchers estimate that extending the term of data exclusivity to 12 years would increase the lifetime revenue of a drug by 5 percent, on average. With empirical evidence that profits drive drug innovation, this longer term would lead to an additional 228 drug approvals over the next fifty years and an increase of 1.7 months in average life expectancy, according to the study.

John Romley, an economist with the Schaeffer Center at USC and research assistant professor at the USC School of Policy, Planning and Development, acknowledged the trade-off between current and future generations.

"Americans in the early 2020's would bear the cost of increasing drug spending. However, people turning 55 in 2060 could expect increased life expectancy as a result of innovation in the interceding years — that is, new drugs brought to market because of lengthier data exclusivity."
FundingThe research was sponsored by the National Institute on Aging through its support of the Roybal Center for Health Policy Simulation and INTERPAT, an association of research-based pharmaceutical companies.
ParticipationJesse D. Malkin at Precision Health Economics and Tomas Philipson of the University of Chicago are also authors on the study.
CitationThe Benefits from Giving Makers of Conventional 'Small Molecule' Drugs Longer Exclusivity Over Clinical Trial Data. Dana P. Goldman, Darius N. Lakdawalla, Jesse D. Malkin, John Romley, and Tomas Philipson. Health Affairs 2011; 30(1): 84-90. doi:10.1377/hlthaff.2009.1056

Abstract

Pharmaceutical companies and generic drug manufacturers have long been at odds over “data exclusivity” regulations. These rules require a waiting period of at least five years before generic drug companies can access valuable clinical trial data necessary to bring less expensive forms of innovative drugs to market. Pharmaceutical companies want the data exclusivity period lengthened to protect their investment. Generic manufacturers want the period shortened so that they can bring less expensive versions of drugs to patients sooner. We examine the long-term effect of extending the data exclusivity period for conventional “small-molecule” drugs to twelve years—the same exclusivity period already extended to large-molecule biologic drugs under the Affordable Care Act. We conclude that Americans would benefit from a longer period of data exclusivity.

Keywords: pharmaceuticals, health promotion, disease prevention, research and technology, health spending.

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TS-Si is dedicated to the acceptance, medical treatment, and legal protection of individuals correcting the misalignment of their brains and their anatomical sex, while supporting their transition into society as hormonally reconstituted and surgically corrected citizens.

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Last Updated on Monday, 10 January 2011 01:31
 
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