Athira Pharma, Inc., Bothell, WA, USA.
J Alzheimers Dis. 2023;92(1):1-12. doi: 10.3233/JAD-220871.
An estimated 6.5 million Americans aged 65 years or older have Alzheimer's disease (AD), which will grow to 13.8 million Americans by 2060. Despite the growing burden of dementia, no fundamental change in drug development for AD has been seen in > 20 years. Currently approved drugs for AD produce only modest symptomatic improvements in cognition with small effect sizes. A growing mismatch exists between the urgent need to develop effective drugs for symptomatic AD and the largely failed search for disease modification. The failure rate of clinical trials in AD is high overall, and in particular for disease-modifying therapies. Research efforts in AD have focused predominantly on amyloid-β and tau pathologies, but limiting clinical research to these "classical hallmarks" of the disease does not address the most urgent patient, caregiver, or societal needs. Rather, clinical research should consider the complex pathophysiology of AD. Innovative approaches are needed that provide outside-the-box thinking, and re-imagine trial design, interventions, and outcomes as well as progress in proteomics and fluid biomarker analytics for both diagnostics and disease monitoring. A new approach offering a highly specific, yet multi-pronged intervention that exerts positive modulation on the HGF/MET neurotrophic system is currently being tested in mid-to-late-stage clinical trials in mild to moderate AD. Findings from such trials may provide data to support novel approaches for development of innovative drugs for treating AD at various disease stages, including among patients already symptomatic, and may offer benefits for other neurodegenerative diseases.
据估计,有 650 万美国老年人患有阿尔茨海默病(AD),到 2060 年,这一数字将增至 1380 万。尽管痴呆症的负担不断增加,但在过去 20 年中,AD 的药物开发并没有出现根本性的变化。目前批准用于 AD 的药物仅能在认知方面产生适度的症状改善,效果较小。在迫切需要开发针对 AD 症状的有效药物与未能成功寻找疾病修饰疗法之间,存在着越来越大的差距。AD 临床试验的总体失败率很高,特别是对于疾病修饰疗法。AD 的研究主要集中在淀粉样蛋白-β和 tau 病理学上,但将临床研究仅限于这些疾病的“经典标志”并不能满足最紧迫的患者、护理人员或社会需求。相反,临床研究应该考虑 AD 的复杂病理生理学。需要创新的方法,提供新颖的思路,重新设计临床试验设计、干预措施和结果,以及在蛋白质组学和液体检生物标志物分析方面取得进展,以用于诊断和疾病监测。目前,一种新的方法正在进行中,该方法提供了一种高度特异性但多管齐下的干预措施,对 HGF/MET 神经营养系统产生积极的调节作用,正在轻度至中度 AD 的中后期临床试验中进行测试。此类试验的结果可能为开发针对不同疾病阶段的 AD 创新药物提供数据支持,包括已经出现症状的患者,并可能为其他神经退行性疾病提供益处。