医学
临床试验
食品药品监督管理局
代理终结点
临床终点
周围神经病变
糖尿病神经病变
定量感官测试
重症监护医学
药品
糖尿病
病理
药理学
感觉系统
神经科学
内分泌学
生物
作者
Ioannis N. Petropoulos,Georgios Ponirakis,Adnan Khan,Hamad Almuhannadi,Hoda Gad,Rayaz A. Malik
标识
DOI:10.4093/dmj.2018.0056
摘要
There are potentially many ways of assessing diabetic peripheral neuropathy (DPN). However, they do not fulfill U.S. Food and Drug Administration (FDA) requirements in relation to their capacity to assess therapeutic benefit in clinical trials of DPN. Over the past several decades symptoms and signs, quantitative sensory and electrodiagnostic testing have been strongly endorsed, but have consistently failed as surrogate end points in clinical trials. Therefore, there is an unmet need for reliable biomarkers to capture the onset and progression and to facilitate drug discovery in DPN. Corneal confocal microscopy (CCM) is a non-invasive ophthalmic imaging modality for in vivo evaluation of sensory C-fibers. An increasing body of evidence from multiple centers worldwide suggests that CCM fulfills the FDA criteria as a surrogate endpoint of DPN.
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