Literature DB >> 18432281

Patenting and licensing in genetic testing: recommendations of the European Society of Human Genetics.

S Aymé1, Gert Matthijs, S Soini.   

Abstract

Patents for inventions can be beneficial for society, if they drive innovation and promote progress. In most areas, the patenting system works satisfactorily. However, it must be recognized that in some instances it can also be problematic; this is the case in the field of genetics, and particularly in the area of genetic testing. As patents should serve their original purpose (promoting innovation through a fair reward system for the inventors), the European Society of Human Genetics (ESHG) suggests ways to improve the mechanisms that already form part of the patents system as a whole. In brief, the ESHG recommends limiting the breadth of the claims in genetic patents and, more practically, to reduce the number of patents by limiting the patentable subject matter, thereby improving the quality of the patents that will eventually be granted. There is also a suggestion to redefine the concept of utility in patent law, by taking account of downstream clinical experience. The ESHG sees no harm in the patenting of novel technical tools for genetic testing (eg PCR or chip technologies), as they can promote investment and still allow for invention around them. Many disputes between supporters of the patenting system and the public revolve around ethical issues. The European Patent Office should consider the benefit of having an ethics committee to consider issues of major interest, such as patents applied to genes. The problem of licensing should also be addressed. Practically, this means supporting the Organisation for Economic Co-operation and Development guidelines, which prescribe that licences should be non-exclusive and easily obtainable, both in practical and in financial terms. To promote this, the practical exploration of alternative models for licensing, like patent pools and clearinghouses, is a prerequisite. To better track developments in this field, the establishment of a voluntary reporting system, whereby geneticists could report on any issues related to new and/or old patents or licences in the light of service provision to patients, would be worthwhile. Finally, the ESHG is calling upon all stakeholders to start the process of developing a code of conduct for partners with patents, covering ethical aspects as well as smooth licensing arrangements.

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Year:  2008        PMID: 18432281     DOI: 10.1038/ejhg.2008.37

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  5 in total

1.  Detection of inherited mutations for hereditary cancer using target enrichment and next generation sequencing.

Authors:  Yanfang Guan; Hong Hu; Yin Peng; Yuhua Gong; Yuting Yi; Libin Shao; Tengfei Liu; Gairui Li; Rongjiao Wang; Pingping Dai; Yves-Jean Bignon; Zhe Xiao; Ling Yang; Feng Mu; Liang Xiao; Zeming Xie; Wenhui Yan; Nan Xu; Dongxian Zhou; Xin Yi
Journal:  Fam Cancer       Date:  2015-03       Impact factor: 2.375

2.  Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing.

Authors:  Tom Walsh; Ming K Lee; Silvia Casadei; Anne M Thornton; Sunday M Stray; Christopher Pennil; Alex S Nord; Jessica B Mandell; Elizabeth M Swisher; Mary-Claire King
Journal:  Proc Natl Acad Sci U S A       Date:  2010-06-28       Impact factor: 11.205

3.  Gene patents and licensing: case studies prepared for the Secretary's Advisory Committee on Genetics, Health, and Society.

Authors:  Robert Cook-Deegan; Christopher Heaney
Journal:  Genet Med       Date:  2010-04       Impact factor: 8.822

Review 4.  Patent pools and clearinghouses in the life sciences.

Authors:  Esther van Zimmeren; Sven Vanneste; Gert Matthijs; Wim Vanhaverbeke; Geertrui Van Overwalle
Journal:  Trends Biotechnol       Date:  2011-07-04       Impact factor: 19.536

5.  Gene patents and personalized medicine - what lies ahead?

Authors:  Subhashini Chandrasekharan; Robert Cook-Deegan
Journal:  Genome Med       Date:  2009-09-28       Impact factor: 11.117

  5 in total

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