Toward Consensus on Benefit Sharing in Genetics Research
Toward Consensus on Benefit Sharing in Genetics Research
批准号:
6532184
负责人:
Jon F. Merz
金额:
$4.85万
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-07-18 至 2004-06-30
中文摘要
描述(由申请人提供):患者团体越来越积极地促进和
促进临床前和临床研究。虽然患者群体长期以来一直在
参与研究,各种团体已经或正在建立资助研究的基金会,
编制特定疾病的患者登记册、家谱和医学数据库,并建立组织和DNA库,为遗传学研究提供关键资源。参与这些倡议的个人及其家人往往直接参与研究。这一不断发展的作用是与生物医学研究的另外两个重大变化同时发生的:技术转让的产生和迅速发展以及生物技术科学和投资的爆炸式增长。与科学家的密切合作关系极大地促进了有针对性的研究,因为它提供了进入受影响社区的机会,在确定和争取这些社区的潜在参与者方面给予积极的协助,为研究人员提供可信度,从而增加信任和参与,并分担招募费用。但是,受试者之间的关系和参与也提出了分享研究成果的公平要求。拟议的会议将
汇集了众多对遗传学研究感兴趣的群体,包括患者和疾病倡导团体,基金会,NIH,研究人员,大学,制药公司和生物技术公司,以及带来知识产权法,经济学和卫生政策方面的学科专业知识。目标不是寻求共识,而是确定关键问题和提出最能满足所有有关各方利益和需要的想法。
英文摘要
DESCRIPTION (provided by applicant): Patient groups are becoming more active in promoting and
facilitating pre-clinical and clinical research. While patient groups have long played a key role in
participating in research, various groups have or are starting foundations for funding research,
compiling disease-specific patient registries and genealogical and medical databases, and establishing tissue and DNA banks to provide resources crucial for genetics research. Individuals involved in these initiatives and their families often participate directly in research. This developing role has occurred concurrently with two other significant changes in biomedical research: the creation and rapid evolution of technology transfer and the explosion in biotechnology science and investment. The close collaborative relationships with scientists greatly facilitate targeted research by providing access to affected communities, giving highly motivated assistance in identifying and soliciting potential participants from these communities, lending credibility to the researchers that can increase trust and participation, and sharing the costs of recruitment. But the relationship and involvement of the subjects also raises equitable claims to share in the financial fruits of research. The proposed conference will
bring together numerous constituencies interested in genetics research, including patient and disease advocacy groups, foundations, the NIH, researchers, universities, pharmaceutical companies, and biotechnology firms, as well as bring disciplinary expertise in intellectual property law, economics, and health policy. The goal is not to find consensus, but to identify key issues and generate ideas to best satisfy the interests and needs of all involved parties.
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