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The revolution re-visited: Clinical and genetics research paradigms and the productivity paradox in drug discovery

机译:重新进行了革命:药物发现中的临床和遗传学研究范式和生产率悖论

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Breakthroughs in genetics and molecular biology in the 1970s and 1980s were heralded as a major technological revolution in medicine that would yield a wave of new drug discoveries. However, some forty years later the expected benefits have not materialized. I question the narrative of biotechnology as a Schumpeterian revolution by comparing it to the academic research paradigm that preceded it, clinical research in hospitals. 1 analyze these as distinct research paradigms that involve different epistemolo-gies, practices, and institutional loci. I develop the claim that the complexity of biological systems means that clinical research was well adapted to medical innovation, and that the genetics/molecular biology paradigm imposed a predictive logic to search that was less effective at finding new drugs. The paper describes how drug discovery unfolds in each paradigm: in clinical research, discovery originates with observations of human subjects and proceeds through feedback-based learning, whereas in the genetics model, discovery originates with a precisely-defined molecular target; feedback from patients enters late in the process. The paper reviews the post-War institutional history that witnessed the relative decline of clinical research and the rise of genetics and molecular science in the United States bio-medical research landscape. The history provides a contextual narrative to illustrate that, in contrast to the framing of biotechnology as a Schumpeterian revolution, the adoption of biotechnology as a core drug discovery platform was propelled by institutional changes that were largely disconnected from processes of scientific or technological selection. Implications for current medical policy initiatives and translational science are discussed.
机译:遗传学和分子生物学在1970年代和1980年代取得的突破被预示为医学领域的重大技术革命,它将掀起一波新药发现浪潮。但是,大约四十年后,预期的收益仍未实现。我将生物技术的叙事与之前的学术研究范式(医院的临床研究)进行比较,从而质疑生物技术作为熊彼特式革命的叙事。 1将它们作为涉及不同认识论,实践和机构位点的独特研究范式进行分析。我提出这样的说法,即生物系统的复杂性意味着临床研究非常适合医学创新,而遗传学/分子生物学范式强加了一种预测性逻辑,以寻找在寻找新药方面不太有效的搜索方式。本文描述了药物发现在每个范式中如何发展:在临床研究中,发现起源于对人类受试者的观察,并通过基于反馈的学习进行,而在遗传学模型中,发现起源于精确定义的分子靶标;来自患者的反馈进入过程的后期。这篇论文回顾了战后的制度历史,见证了临床研究相对衰落以及遗传学和分子科学在美国生物医学研究领域的兴起。历史提供了一个背景叙事,以说明与将生物技术构想为熊彼特式革命相反,生物技术作为核心药物发现平台的采用是受到体制变革的推动,而体制变革与科学或技术选择过程大体上是脱节的。讨论了对当前医疗政策计划和转化科学的影响。

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