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首页> 外文期刊>Therapeutic innovation & regulatory science. >Coalition Against Major Diseases: Precompetitive Collaborations and Regulatory Paths to Accelerating Drug Development for Neurodegenerative Diseases
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Coalition Against Major Diseases: Precompetitive Collaborations and Regulatory Paths to Accelerating Drug Development for Neurodegenerative Diseases

机译:反对主要疾病的联盟:竞争前的合作和加速神经退行性疾病药物开发的监管途径

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摘要

Precompetitive collaborations have been successful in several disease areas and industries. Such collaborations are critical to address the gaps and challenges in therapeutic development for chronic neurodegenerative diseases. On November 5, 2012, members of the scientific community, advocates, regulators, industry, and government officials met at the US Food and Drug Administration to develop tools to expedite drug development and maximize the potential for success in future drug trials for Alzheimer disease and Parkinson disease. The meeting established that multiple collaborative approaches are essential for accelerating drug development. Such approaches include precompetitive data sharing, regulatory qualification of biomarkers and clinical outcome assessments, implementation of data standards, and development of quantitative drug disease trial models. While challenges to collaboration among industry partners are formidable, they are not insurmountable. The Coalition Against Major Diseases (CAMD) has several positive examples to highlight. This review represents proceedings from CAMD's annual conference and discusses the key themes that are being advanced by the Critical Path Institute.
机译:竞争前的合作已经在多个疾病领域和行业中取得了成功。这种合作对于解决慢性神经退行性疾病的治疗发展中的差距和挑战至关重要。 2012年11月5日,科学界的成员,拥护者,监管者,行业和政府官员在美国食品和药物管理局举行了会议,以开发加速药物开发的工具,并最大程度地提高阿尔茨海默氏病和帕金森综合症。会议确定了多种协作方法对于加速药物开发至关重要。这些方法包括竞争前的数据共享,生物标志物的监管资格和临床结果评估,数据标准的实施以及药物性疾病定量试验模型的开发。尽管行业合作伙伴之间的协作面临巨大挑战,但并非无法克服。重大疾病联盟(CAMD)有几个积极的例子值得强调。此次审查代表了CAMD年度会议的议事情况,并讨论了关键路径研究所提出的关键主题。

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