亨廷顿氏病监管科学联盟:加速医疗产品开发。

IF 2.1 Q3 NEUROSCIENCES
Emily C. Turner, Emily C. Gantman, C. Sampaio, Sudhir Sivakumaran
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引用次数: 1

摘要

亨廷顿氏病(HD)是一种毁灭性的神经退行性疾病,迫切需要改善疾病的治疗方法。为此,合作使该领域的临床研究实践标准化并推动应对药物开发挑战的进展至关重要。在2017年由CHDI基金会和关键路径研究所组织的一次会议上,制药行业、学术界、监管机构和患者倡导团体的利益相关者讨论了成立一个致力于HD监管科学的联盟的必要性和潜在影响。因此,亨廷顿病监管科学联盟(HD- rsc)成立了,这是一个致力于建立监管战略以加快亨廷顿病治疗药物批准的竞争前联盟。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Huntington's Disease Regulatory Science Consortium: Accelerating Medical Product Development.
Huntington's disease (HD) is a devastating neurodegenerative disorder that urgently needs disease-modifying therapeutics. To this end, collaboration to standardize clinical research practices in the field and drive progress in addressing drug development challenges is paramount. At a meeting in 2017 organized by CHDI Foundation and the Critical Path Institute, stakeholders across the pharmaceutical industry, academia, regulatory agencies, and patient advocacy groups discussed the need for and potential impact of a consortium dedicated to HD regulatory science. Consequently, the Huntington's Disease Regulatory Science Consortium (HD-RSC) was formed, a precompetitive consortium that is dedicated to building a regulatory strategy to expedite the approval of HD therapeutics.
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来源期刊
CiteScore
4.80
自引率
9.70%
发文量
60
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