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加速双食欲素受体拮抗剂 ACT-541468 的开发:在首例人体研究中整合微示踪剂。

Accelerated Development of the Dual Orexin Receptor Antagonist ACT-541468: Integration of a Microtracer in a First-in-Human Study.

机构信息

Department of Clinical Pharmacology, Idorsia Pharmaceuticals Ltd, Allschwil, Switzerland.

Centre for Human Drug Research (CHDR), Leiden, The Netherlands.

出版信息

Clin Pharmacol Ther. 2018 Nov;104(5):1022-1029. doi: 10.1002/cpt.1046. Epub 2018 Mar 10.

Abstract

The orexin system regulates sleep and arousal and is targeted by ACT-541468, a new dual orexin receptor antagonist (DORA). Healthy male subjects received a single oral dose of 5-200 mg to assess safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), mass balance, metabolism, and absolute bioavailability utilizing a C-labeled, orally and intravenously (i.v.) administered microtracer. The drug was safe and well tolerated; the PK profile was characterized by quick absorption and elimination, with median time to reach maximum concentration (t ) of 0.8-2.8 h and geometric mean terminal half-life (t ) of 5.9-8.8 h. Clear dose-related effects on the central nervous system were observed at ≥25 mg, indicating a suitable PK-PD profile for a sleep-promoting drug, allowing for rapid onset and duration of action limited to the intended use. This comprehensive first-in-human study created a wealth of data, while saving resources in drug development.

摘要

食欲素系统调节睡眠和觉醒,ACT-541468 是一种新型的双重食欲素受体拮抗剂(DORA),可作用于该系统。健康男性受试者单次口服 5-200mg,评估安全性、耐受性、药代动力学(PK)、药效动力学(PD)、物质平衡、代谢和绝对生物利用度,采用 C 标记的口服和静脉内(i.v.)给予微示踪剂。该药物安全且耐受良好;PK 特征为快速吸收和消除,中位达峰时间(t )为 0.8-2.8h,几何平均终末半衰期(t )为 5.9-8.8h。≥25mg 时观察到中枢神经系统的剂量相关性作用,表明具有适合促进睡眠药物的 PK-PD 特征,允许快速起效和作用持续时间限于预期用途。这项全面的首次人体研究产生了大量数据,同时节省了药物开发的资源。

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