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用于器官移植药物研发的生物标志物的鉴定

Qualification of biomarkers for drug development in organ transplantation.

作者信息

Burckart Gilbert J, Amur Shashi, Goodsaid Federico M, Lesko Lawrence J, Frueh Felix W, Huang Shiew-Mei, Cavaille-Coll Marc W

机构信息

School of Pharmacy, University of Southern California, Los Angeles, CA, USA.

出版信息

Am J Transplant. 2008 Feb;8(2):267-70. doi: 10.1111/j.1600-6143.2007.02063.x. Epub 2007 Dec 18.

Abstract

The drug development process is dependent upon having established end points for measuring drug efficacy and adverse effects. New drug development in organ transplantation suffers from having end points which are either outdated or which do not serve the purpose of addressing the current critical drug therapy problems. Numerous biomarkers have been examined in organ transplantation, but almost all would be classified as exploratory for drug development purposes. Some of the possible pathways out of this dilemma include investigator- or consortium-initiated research that would qualify the biomarkers as either probable or known valid biomarkers, help in identification of new end points in transplantation and their associated biomarkers, co-development of a new biomarker and drug for transplantation and the use of new clinical trial design methods which facilitate enriched or stratified transplant patient populations. With new biomarkers and new study design methodologies for drug development, improvement in the drug development process for transplantation is a real possibility that the transplant clinical and research community can help to bring about.

摘要

药物研发过程依赖于已确立的用于衡量药物疗效和不良反应的终点指标。器官移植领域的新药研发面临终点指标过时或无法解决当前关键药物治疗问题的困境。在器官移植中已对众多生物标志物进行了研究,但几乎所有这些生物标志物从药物研发目的来看都属于探索性的。摆脱这一困境的一些可能途径包括研究者或研究联盟发起的研究,这些研究可将生物标志物鉴定为可能的或已知有效的生物标志物,有助于识别移植中的新终点指标及其相关生物标志物,共同研发用于移植的新生物标志物和药物,以及使用有助于富集或分层移植患者群体的新临床试验设计方法。借助用于药物研发的新生物标志物和新研究设计方法,移植药物研发过程确实有可能得到改进,而移植临床和研究界能够助力实现这一点。

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