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Safety tolerability and efficacy of the glutaminyl cyclase inhibitor PQ912 in Alzheimer’s disease: results of a randomized double-blind placebo-controlled phase 2a study

机译:谷氨酰环化酶抑制剂PQ912在阿尔茨海默氏病中的安全性耐受性和功效:一项随机双盲安慰剂对照2a期研究的结果

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摘要

BackgroundPQ912 is an inhibitor of the glutaminyl cyclase enzyme that plays a central role in the formation of synaptotoxic pyroglutamate-A-beta oligomers. We report on the first clinical study with PQ912 in subjects with biomarker-proven Alzheimer’s disease (AD). The aim was to determine the maximal tolerated dose, target occupancy and treatment-related pharmacodynamic effects. The exploratory efficacy readouts selected were tailored to the patient population with early AD. The therapeutic approach focuses on synaptic dysfunction as captured by various measures such as electroencephalography (EEG), synaptic biomarkers and sensitive cognitive tests.
机译:背景PQ912是谷氨酰胺酰环化酶的抑制剂,在突触毒性焦谷氨酸-A-β低聚物的形成中起着核心作用。我们报告了P​​Q912在具有生物标志物证明的阿尔茨海默氏病(AD)的受试者中进行的首次临床研究。目的是确定最大耐受剂量,目标占有率和与治疗有关的药效学作用。所选的探索性功效读数是针对早期AD患者的量身定制的。治疗方法侧重于通过各种措施捕获的突触功能障碍,例如脑电图(EEG),突触生物标记和敏感的认知测试。

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