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Application of biomarkers in the development of drugs intended for the treatment of osteoarthritis

机译:生物标志物在开发用于治疗骨关节炎的药物中的应用

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摘要

Objective: Osteoarthritis (OA) is a chronic and slowly progressive disease for which biomarkers may be able to provide a more rapid indication of therapeutic responses to therapy than is currently available; this could accelerate and facilitate OA drug discovery and development programs. The goal of this document is to provide a summary and guide to the application of in vitro (biochemical and other soluble) biomarkers in the development of drugs for OA and to outline and stimulate a research agenda that will further this goal. Methods: The Biomarkers Working Group representing experts in the field of OA biomarker research from both academia and industry developed this consensus document between 2007 and 2009 at the behest of the Osteoarthritis Research Society International Federal Drug Administration initiative (OARSI FDA initiative). Results: This document summarizes definitions and classification systems for biomarkers, the current outcome measures used in OA clinical trials, applications and potential utility of biomarkers for development of OA therapeutics, the current state of qualification of OA-related biomarkers, pathways for biomarker qualification, critical needs to advance the use of biomarkers for drug development, recommendations regarding practices and clinical trials, and a research agenda to advance the science of OA-related biomarkers. Conclusions: Although many OA-related biomarkers are currently available they exist in various states of qualification and validation. The biomarkers that are likely to have the earliest beneficial impact on clinical trials fall into two general categories, those that will allow targeting of subjects most likely to either respond and/or progress (prognostic value) within a reasonable and manageable time frame for a clinical study (for instance within 1-2 years for an OA trial), and those that provide early feedback for preclinical decision-making and for trial organizers that a drug is having the desired biochemical effect. As in vitro biomarkers are increasingly investigated in the context of specific drug treatments, advances in the field can be expected that will lead to rapid expansion of the list of available biomarkers with increasing understanding of the molecular processes that they represent. (C) 2011 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.
机译:目的:骨关节炎(OA)是一种慢性缓慢进展的疾病,对于该疾病,生物标志物可能能够提供比目前更快速的治疗反应指示;这可以加快和促进OA药物的发现和开发计划。本文档的目的是提供摘要和指导,以体外(生物化学和其他可溶性)生物标志物在OA药物开发中的应用,并概述和刺激将推动这一目标的研究议程。方法:代表骨关节炎研究协会国际联邦药物管理局倡议(OARSI FDA倡议),由学术界和工业界的OA生物标志物研究领域的专家组成的生物标志物工作组在2007年至2009年之间制定了该共识文件。结果:该文件概述了生物标志物的定义和分类系统,OA临床试验中使用的当前结果指标,生物标志物在OA治疗药物开发中的应用和潜在用途,OA相关生物标志物的鉴定现状,生物标志物鉴定的途径,迫切需要促进将生物标志物用于药物开发,有关实践和临床试验的建议以及促进与OA相关的生物标志物科学的研究议程。结论:尽管目前可获得许多与OA相关的生物标记,但它们以各种鉴定和验证状态存在。可能对临床试验产生最早的有益影响的生物标志物可分为两大类,即能够靶向最可能在合理且可管理的临床时间内响应和/或进展的患者(预后价值)的生物标志物。研究(例如OA试验在1-2年内),以及那些为临床前决策和试验组织者提供早期反馈的药物具有所需生化作用的药物。随着在特定药物治疗的背景下对体外生物标记物的研究越来越多,可以预见该领域的进展,随着对它们代表的分子过程的日益了解,将导致可用生物标记物列表的迅速扩展。 (C)2011年国际骨关节炎研究学会。由Elsevier Ltd.出版。保留所有权利。

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