An Open-Label, Pilot Study of Daratumumab SC in Mild to Moderate Alzheimer's Disease.

IF 2.8 Q2 NEUROSCIENCES
Journal of Alzheimer's disease reports Pub Date : 2024-07-31 eCollection Date: 2024-01-01 DOI:10.3233/ADR-240089
Marc L Gordon, Erica Christen, Lynda Keehlisen, Michelle Gong, Fung Lam, Luca Giliberto, Jesus J Gomar, Jeremy Koppel
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引用次数: 0

Abstract

We conducted a small, open-label, pilot study of daratumumab to explore target engagement, safety, and potential efficacy in patients with mild to moderate Alzheimer's disease. Daratumumab SC 1800 mg was given subcutaneously weekly for 8 weeks, then every 2 weeks for 16 weeks. Flow cytometry to measure the CD38+ proportion of CD8 + CD4- T cells and cognitive assessments were performed at baseline, day 176, and day 246. Daratumumab significantly reduced CD38 + CD8 + CD4- T cells after 24 weeks and this effect persisted 11 weeks thereafter. There was no hematological toxicity or unexpected adverse events. Responder analysis showed no improvement on cognitive outcome measures.

一项针对轻度至中度阿尔茨海默病的 Daratumumab SC 开放标签试验性研究。
我们对达拉单抗进行了一项小型、开放标签的试验性研究,以探索轻度至中度阿尔茨海默病患者的靶点参与、安全性和潜在疗效。Daratumumab SC 1800 毫克每周皮下注射一次,共注射 8 周,然后每两周注射一次,共注射 16 周。在基线、第176天和第246天分别进行了流式细胞术检测CD38+ CD8 + CD4- T细胞比例和认知评估。达拉土单抗在24周后明显减少了CD38 + CD8 + CD4- T细胞,这种效应在此后11周持续存在。没有出现血液毒性或意外不良事件。应答者分析显示,认知结果指标没有改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
2.80
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