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Translational Biomarkers and Ex Vivo Models of Joint Tissues as a Tool for Drug Development in Rheumatoid Arthritis

机译:平移生物标志物和关节组织的体内模型作为类风湿关节炎药物开发的工具

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摘要

ObjectiveRheumatoid arthritis (RA) is a chronic and degenerative autoimmune joint disease that leads to disability, reduced quality of life, and increased mortality. Although several synthetic and biologic disease‐modifying antirheumatic drugs are available, there is still a medical need for novel drugs that control disease progression. As only 10% of experimental drug candidates for treatment of RA that enter phase I trials are eventually registered by the Food and Drug Administration, there is an immediate need for translational tools to facilitate early decision‐making in drug development. In this study, we aimed to determine if the inability of fostamatinib (a small molecule inhibitor of Syk) to demonstrate sufficient efficacy in phase III of a previous clinical study could have been predicted earlier in the development process.
机译:目的类风湿关节炎(RA)是一种慢性变性性自身免疫性关节疾病,可导致残疾,生活质量下降和死亡率增加。尽管有几种合成的和可改善生物疾病的抗风湿药,但医学上仍需要控制疾病进展的新药。由于进入I期试验的仅10%的用于RA治疗的实验性药物候选者最终获得了美国食品和药物管理局(FDA)的注册,因此迫切需要使用翻译工具来促进药物开发的早期决策。在这项研究中,我们旨在确定是否可以在开发过程的较早阶段就预测出fostamatinib(Syk的小分子抑制剂)无法在先前临床研究的III期中证明足够的疗效。

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