阿尔茨海默病药物试验采用癌症的多靶点策略

阿尔茨海默病试验正转向受癌症研究启发的多靶点方法,即便Novo Nordisk的司美格鲁肽试验失败。只有两种药物——Eli Lilly的Kisunla和Eisai与Biogen的Leqembi——被广泛批准用于减缓疾病进展。这种演变将这种脑部退化疾病视为复杂系统,在其全球影响下寻求新的遏止途径。

阿尔茨海默病导致全球超过5500万痴呆病例中的约60%,其特征是大脑中淀粉样蛋白和tau蛋白积聚。

目前仅有两种药物被广泛批准用于减缓其进展:Eli Lilly的Kisunla和Eisai与Biogen的Leqembi。这两种药物通过清除有毒的淀粉样蛋白斑块,将进展速度降低约30%。

专家们强调试验中的关键转变,例如Novo Nordisk的重磅GLP-1药物司美格鲁肽用于阿尔茨海默病的试验失败。这些努力凸显了将这种脑部退化疾病视为复杂通路网络的观点,类似于癌症治疗领域的近期变革。

借鉴癌症的多靶点策略,研究人员正在推进工作,以识别更多靶点和方法,更全面地阻断该疾病。

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