Diagnostic Kits/The Argument Framework: Difference between revisions

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we should cover asap the following bibliography...
== Outstanding Questions ==
Our debate should be structured around the debate from IP scholars ("problems with patents") and what the empirical research points to ("not that much problem with patents")...we need to understand clearly both sides and be able to write about it
Finally, how they impact in kits...remembering the research inputs (genetic information, for instance) is different from research output (a product, such as a kit)


  1. our debate should be structured around the debate from IP scholars ("problems with patents") and what the empirical research points to ("not that much problem with patents")...we need to understand clearly both sides and be able to write about it
Thus, while we may have a "research commons" being formed by projects such as the human genomics + scientific practices of ignoring patents (as stated in the June report), we may have blocking patents later on the research outputs  
  2. finally, how they impact in kits...remembering the research inputs (genetic information, for instance) is different from research output (a product, such as a kit)
 
  3. thus, while we may have a "research commons" being formed by projects such as the human genomics + scientific practices of ignoring patents (as stated in the June report), we may have blocking patents later on the research outputs  
* MTAs?
* Do perceived patent licensing / infringement concerns convince researchers to focus on other areas?
* Do exclusive non-sublicensed patent licenses limit incremental improvement?  Do non-exclusively licensed diagnostics experience more incremental improvement than exclusively licensed diagnostics?
* Do exclusive licenses limit consumer access to genetic diagnostic products (cost and/or access?) 


== Despite patent challenges, research continues ==
== Despite patent challenges, research continues ==

Revision as of 15:20, 20 November 2009

Outstanding Questions

Our debate should be structured around the debate from IP scholars ("problems with patents") and what the empirical research points to ("not that much problem with patents")...we need to understand clearly both sides and be able to write about it

Finally, how they impact in kits...remembering the research inputs (genetic information, for instance) is different from research output (a product, such as a kit)

Thus, while we may have a "research commons" being formed by projects such as the human genomics + scientific practices of ignoring patents (as stated in the June report), we may have blocking patents later on the research outputs

  • MTAs?
  • Do perceived patent licensing / infringement concerns convince researchers to focus on other areas?
  • Do exclusive non-sublicensed patent licenses limit incremental improvement? Do non-exclusively licensed diagnostics experience more incremental improvement than exclusively licensed diagnostics?
  • Do exclusive licenses limit consumer access to genetic diagnostic products (cost and/or access?)

Despite patent challenges, research continues

Interviews with personnel from firms, universities, and other organizations indicate that biomedical research typically proceeds despite challenges posed by a growing number of patents on research tools. Respondents address these challenges with licensing, inventing around patents, going offshore, the development and use of public databases and research tools, court challenges, and simply using the technology without a license (i.e., infringement), often informally invoking a de facto broad "research exemption."

Biotech IP literature focus

Patents on genomic materials vs. compound "composition of matter" patents

The bulk of the "IP literature" around patents in biotechnology focuses either on (1) the number of patents on genomic materials (i.e., "50% of the genome is patented!") or (2) around the impact of the use of compound "composition of matter" patents on maintaining high drug prices and preventing generic manufacture.

Empirical analysis of the impact of gene patents on research is absent from the literature

While the impact of patents on drug prices is undeniable and carries a brutal human cost, very little literature is based on systematic, empirical analysis of the impact of the gene patents on research itself.

Are gene patents used in a method similar to drug patents?

Gene patents can, and occasionally are, used in a method similar to a drug patent. This occurs most frequently in gene diagnostic testing kits, which carry a regulatory profile similar to drugs, and similar if lower costs

The majority of gene patents are held by universities and remain unlicensed

But the vast majority of gene patents are obtained by universities and unlicensed, or by companies and unprosecuted.

Empirical studies suggest the negative impact gene patents have on research is limited

Thus, the empirical surveys of research laboratories in genomics and proteomics report almost no negative impacts of patents on research.

Choice of research is unaffected by patent activity

It is essential to distinguish between the number of patents extant on genetic materials, the impact of chemical patents on drug prices, the impact of genetic patents on diagnostic kits, and the day-to-day operations of a research lab. While much time and effort has been invested in chronicles of the first three, the consensus is that there is little impact on the fourth.