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学术机构在罕见病和被忽视疾病药物研发中的作用。

The role of academic institutions in the development of drugs for rare and neglected diseases.

机构信息

Center for Orphan Drug Research, Department of Experimental and Clinical Pharmacology, College of Pharmacy, University of Minnesota, Minneapolis, MN, USA.

出版信息

Clin Pharmacol Ther. 2012 Aug;92(2):193-202. doi: 10.1038/clpt.2012.83. Epub 2012 Jul 4.

Abstract

There are approximately 7,000 rare disorders, many of which are life-threatening. Diagnosis is often problematic, and therapies are few. Before the passage of the Orphan Drug Act in 1983, neither the pharmaceutical industry nor universities devoted much effort to research on rare diseases. Important changes have occurred within and outside universities that position them to play a significant role in developing orphan drugs. Several models are being employed to promote drug-related research, including disease-focused, discovery-focused, development-focused, and industry-partnership-focused approaches. However, significant barriers challenge universities' ability to fully contribute to orphan drug development. Academic institutions, along with industry, government, and not-for-profit organizations, must address these issues in order to advance the field. New initiatives designed to increase university-based orphan drug research include creating mechanisms to ensure program continuity, building research and regulatory support infrastructure, facilitating commercialization, expanding government support, and developing mutually beneficial partnerships among academe, industry, and government.

摘要

大约有 7000 种罕见疾病,其中许多疾病是危及生命的。诊断通常存在问题,而且治疗方法很少。在 1983 年《孤儿药法案》通过之前,制药行业和大学都没有投入太多精力研究罕见疾病。大学内部和外部都发生了重要变化,使它们能够在开发孤儿药方面发挥重要作用。目前正在采用几种模式来促进与药物相关的研究,包括以疾病为重点、以发现为重点、以开发为重点和以产业伙伴关系为重点的方法。然而,大学充分参与孤儿药开发的能力面临着重大障碍。学术机构必须与行业、政府和非营利组织一起解决这些问题,以推动该领域的发展。旨在增加大学基础孤儿药研究的新举措包括建立机制以确保项目的连续性,建立研究和监管支持基础设施,促进商业化,扩大政府支持,以及在学术界、产业界和政府之间建立互利的伙伴关系。

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