Fixing the paradigm for biopharmaceutical R&D: Where to start?

C. Milne
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引用次数: 8

Abstract

The basic thesis of this paper is that the R&D sector of the new medicines' business is experiencing evolutionary stress. Due to the failure of the regulatory framework and applied sciences to keep pace with advances in discovery, there is a bottleneck in the development phase of R&D. While improved process may help, there are still problems related to the products themselves, such as the need to move from a population-based model of product development, in which one size fits all, to a more targeted approach based on specialty drugs for patient subpopulations. The old paradigm dominated by big pharma and blockbusters must evolve, in order for a new bio-pharmaceutical paradigm to emerge. Despite the challenge that the fates of the pharmaceutical and biotech sectors are currently intertwined, it may be the dark before the dawn that betokens real change.
修复生物制药研发模式:从哪里开始?
本文的基本论点是新药研发部门正经历着进化压力。由于监管框架和应用科学未能跟上发现的步伐,在研发的发展阶段存在瓶颈。虽然改进的过程可能会有所帮助,但与产品本身有关的问题仍然存在,例如需要从基于人群的产品开发模式(一刀切)转向基于针对患者亚群体的特殊药物的更有针对性的方法。为了让新的生物制药模式出现,由大型制药公司和大片公司主导的旧模式必须进化。尽管制药和生物技术行业的命运目前交织在一起,但可能是黎明前的黑暗,预示着真正的变化。
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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