Petersen Ronald C, Graf Ana, Brady Chris, De Santi Susan, Florian Hana, Landen Jaren, Pontecorvo Mike, Randolph Christopher, Sink Kaycee, Carrillo Maria, Weber Christopher J
Department of Neurology Mayo Clinic Rochester Minnesota USA.
Novartis Pharma AG Basel Switzerland.
Alzheimers Dement (N Y). 2025 Feb 11;11(1):e70038. doi: 10.1002/trc2.70038. eCollection 2025 Jan-Mar.
The design of clinical trials in Alzheimer's disease (AD) must consider the development of new plasma, cerebrospinal fluid (CSF), and imaging biomarkers. They must also define clinically meaningful outcomes for patients and set endpoints that measure these outcomes accurately. With the accelerated United States Food and Drug Administration (FDA) approval of the first anti-amyloid, disease-modifying treatment for AD, a monoclonal antibody called aducanumab, the landscape of clinical trial design is evolving. Enrolment in clinical trials may be impacted by the availability of this and other treatments, and trial design must take into consideration that patients may desire a disease-modifying treatment rather than potentially being randomized to the placebo arm. The Alzheimer's Association Research Roundtable (AARR) Fall 2021 meeting discussed the consideration of well-defined AD staging criteria in protocol design and how they influence more standardized inclusion/exclusion criteria for trials, as well as what constitutes meaningful differentiation between the stages. Discussion explored the current state of knowledge regarding biomarkers and how they can inform AD staging criteria, as many trials are now designed based on specific biomarker features, further underscoring the importance of coordinating AD staging criteria and biomarkers. The relationship between cognition and biomarkers has been studied and this must continue as trials move forward. Researchers, patients, clinicians, regulatory scientists, and payers discussed the state of the field as well as the future of symptomatic Alzheimer's disease clinical trials.
The Alzheimer's Association Research Roundtable (AARR) convened leaders from academia and industry as well as patients, care partners, clinicians, regulators, and payers to discuss the topic of operationalizing selection criteria for clinical trials and the role of biomarkers.Well-defined Alzheimer's disease (AD) staging criteria are an important consideration in study protocol design.Staging criteria and biomarkers must be coordinated to yield high-quality clinical trial results that have meaning for patients with AD by selecting a population most likely to benefit from a specific treatment.
阿尔茨海默病(AD)临床试验的设计必须考虑新型血浆、脑脊液(CSF)和影像学生物标志物的发展。它们还必须为患者定义具有临床意义的结局,并设定能够准确测量这些结局的终点。随着美国食品药品监督管理局(FDA)加速批准了首个用于AD的抗淀粉样蛋白、疾病修饰疗法——一种名为阿杜卡努单抗的单克隆抗体,临床试验设计的格局正在演变。临床试验的入组情况可能会受到这种及其他疗法可用性的影响,并且试验设计必须考虑到患者可能希望接受疾病修饰疗法,而不是可能被随机分配到安慰剂组。阿尔茨海默病协会研究圆桌会议(AARR)2021年秋季会议讨论了在方案设计中考虑明确的AD分期标准,以及它们如何影响更标准化的试验纳入/排除标准,以及各阶段之间有意义的差异是什么。讨论探讨了关于生物标志物的当前知识状态,以及它们如何为AD分期标准提供信息,因为现在许多试验都是基于特定的生物标志物特征设计的,这进一步强调了协调AD分期标准和生物标志物的重要性。认知与生物标志物之间的关系已经得到研究,并且随着试验的推进这一研究必须继续。研究人员、患者、临床医生、监管科学家和支付方讨论了该领域的现状以及有症状阿尔茨海默病临床试验的未来。
阿尔茨海默病协会研究圆桌会议(AARR)召集了学术界和产业界的领导者以及患者、护理伙伴、临床医生、监管人员和支付方,讨论临床试验选择标准的实施主题以及生物标志物的作用。明确的阿尔茨海默病(AD)分期标准是研究方案设计中的一个重要考虑因素。分期标准和生物标志物必须相互协调,通过选择最有可能从特定治疗中获益的人群,得出对AD患者有意义的高质量临床试验结果。