Neuroenhancement Patentability and the Boundaries Conundrum in Psychiatric Disorders

IF 0.2 Q4 LAW
Riccardo Vecellio Segate
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引用次数: 0

Abstract

Patent offices worldwide deny patentability to innovations which stand against the ordre public: does enhancement represent a value-laden societal threat? Patent offices also reject applications for therapeutical methods: when is enhancement also a therapeutical method? One specific class of enhancers, i.e. pharmaceutical neuroenhancers, is particularly complex in this respect: certain molecules can potentially function both as treatment for neuropsychiatric disorders and as recreational enhancers for non-patients’ brain. Hence, the present work advances the debate on enhancement patentability in two directions: ratione loci, by scrutinising China’s stances on enhancement’s safety and morality, compared to the most frequently explored Western jurisdictions, namely the EU and the US; and ratione materiae, by illuminating the porous bioethical boundaries between treatment and enhancement in the domain of neuropsychiatry. It challenges patent offices’ de facto regulatory role in defining and policing citizens’ access to neuroenhancing substances through misplaced or pseudo-scientific intellectual-property narratives of innovativeness and morale.
神经增强专利性与精神疾病的界限难题
全世界的专利局都拒绝为违反公共秩序的创新授予专利权:增强功能是否代表了一种价值上的社会威胁?专利局也拒绝治疗方法的申请:什么时候增强也是一种治疗方法?在这方面,一类特殊的增强剂(即药物神经增强剂)尤为复杂:某些分子既可以治疗神经精神疾病,也可以作为非患者大脑的娱乐性增强剂。因此,本研究从两个方面推进了关于增强剂专利性的讨论:属地原则,与最常探讨的西方司法管辖区(即欧盟和美国)相比,研究中国在增强剂的安全性和道德性方面的立场;属事原则,阐明神经精神疾病领域中治疗和增强之间存在的生物伦理界限。它质疑了专利局在界定和监管公民获取神经增强物质方面所扮演的事实上的监管角色,这种监管是通过错位的或伪科学的创新性和道德性知识产权叙事来实现的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.60
自引率
0.00%
发文量
19
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