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Clinical drug development for dementia with Lewy bodies: past and present

机译:痴呆症患有Lewy Stodies的临床药物开发:过去和现在

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ABSTRACT Introduction: Dementia with Lewy bodies (DLB) is an under-researched area despite being the second most common type of degenerative dementia after Alzheimer's disease. It is an area of unmet need with no approved symptomatic or disease-modifying therapies. The pharmacological management of DLB is complex and challenging because early trials of drugs for DLB have resulted in no demonstrable efficacy. Randomized controlled trials (RCTs) in the DLB population have only recently been initiated. Understanding results from previous and current clinical trials in DLB can provide insights for future research and development. Areas covered: We provide an overview of the DLB drug development landscape and the current treatment strategies. We reviewed ClinicalTrials.gov to identify all clinical trials for the treatment of DLB. Expert opinion: DLB drug development has significantly improved in recent years with eight agents now in clinical trials. However, more rigorous RCTs are urgently needed. Diagnostic criteria must be optimized to accurately diagnose patients for clinical trials and care. New biomarker strategies are necessary to improve diagnostic capabilities and trial designs, and novel drug targets should be identified to develop DLB specific disease-modifying therapies. Evaluating the current drug development landscape can provide insight into how best to optimize development practices.
机译:摘要介绍:痴呆症与lewy尸体(DLB)是一个研究的下面的地区,尽管是阿尔茨海默病后的第二种最常见的退化性痴呆类型。它是未受满足的需求,没有批准的症状或疾病修饰疗法。 DLB的药理学管理是复杂的和挑战性,因为DLB的药物的早期试验导致了没有明显的疗效。 DLB人口中的随机对照试验(RCT)才已启动。在DLB中的先前和当前临床试验的理解结果可以为未来的研发提供见解。涵盖了地区:我们提供DLB药物开发景观和当前治疗策略的概述。我们回顾了Clinicaltrials.gov以确定治疗DLB的所有临床试验。专家意见:近年来,DLB药物发育在临床试验中八年有八个代理商。但是,迫切需要更严格的RCT。必须优化诊断标准,以准确诊断患者进行临床试验和护理。新的生物标志物策略是改善诊断能力和试验设计所必需的,并且应识别新的药物靶标以发展DLB特异性疾病改性疗法。评估目前的药物开发景观可以深入了解如何最好地优化开发实践。

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