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在健康受试者中多次给予新型鞘氨醇-1-磷酸受体1调节剂LC51-0255后,淋巴细胞计数和心率呈剂量依赖性降低。

Dose-dependent reduction of lymphocyte count and heart rate after multiple administration of LC51-0255, a novel sphingosine-1-phosphate receptor 1 modulator, in healthy subjects.

作者信息

Hwang Inyoung, Lee Sang Won, Oh Jaeseong, Lee SeungHwan, Jang In-Jin, Yu Kyung-Sang

机构信息

Department of Clinical Pharmacology and Therapeutics, Seoul National University College of Medicine and Hospital, Seoul, South Korea.

Department of Clinical Pharmacology and Therapeutics, Hanyang University Seoul Hospital, Seoul, South Korea.

出版信息

Front Pharmacol. 2022 Aug 22;13:930615. doi: 10.3389/fphar.2022.930615. eCollection 2022.

Abstract

Sphingosine-1-phosphate receptor mediates the egress of lymphocytes from lymphoid organs, and its inhibition results in a decreased number of circulating lymphocytes. The aim of the current study was to investigate the safety and pharmacodynamic and pharmacokinetic characteristics of a novel sphingosine-1-phosphate receptor modulator, LC51-0255. A phase 1 randomized, double-blind, placebo-controlled, multiple dosing, dose-escalation study was conducted on healthy Korean male subjects. After single and daily administration of LC51-0255 for 21 days, a dose-dependent decrease in lymphocyte count and heart rate was observed through 0.25-2 mg dose range of LC51-0255. The mean elimination half-life of LC51-0255 was 76-95 h. LC51-0255 was accumulated with a mean accumulation ratio of 5.17-6.64. During the study, LC51-0255 was generally well tolerated. The most common treatment-emergent adverse event was bradycardia. No clinically significant event of arrhythmia, including AV block, was observed. No clinically significant difference in blood pressure was observed between the dose groups. In other safety assessments, no clinically significant abnormalities were observed, except for bradycardia. Daily administration of LC51-0255 in the range of 0.25-2 mg resulted in a dose-dependent reduction of lymphocyte counts and heart rate. LC51-0255 is generally safe and well tolerated in healthy volunteers.

摘要

1-磷酸鞘氨醇受体介导淋巴细胞从淋巴器官中流出,抑制该受体可导致循环淋巴细胞数量减少。本研究的目的是调查一种新型1-磷酸鞘氨醇受体调节剂LC51-0255的安全性、药效学和药代动力学特征。在健康韩国男性受试者中进行了一项1期随机、双盲、安慰剂对照、多次给药、剂量递增研究。在单次和每日给予LC51-0255 21天后,在LC51-0255 0.25至2毫克剂量范围内观察到淋巴细胞计数和心率呈剂量依赖性下降。LC51-0255的平均消除半衰期为76至95小时。LC51-0255有蓄积,平均蓄积比为5.17至6.64。在研究期间,LC51-0255总体耐受性良好。最常见的治疗中出现的不良事件是心动过缓。未观察到包括房室传导阻滞在内的心律失常的临床显著事件。各剂量组之间未观察到血压的临床显著差异。在其他安全性评估中,除心动过缓外,未观察到临床显著异常。每日给予0.25至2毫克范围内的LC51-0255可导致淋巴细胞计数和心率呈剂量依赖性降低。LC51-0255在健康志愿者中总体安全且耐受性良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b796/9442045/95971e3acaf4/fphar-13-930615-g001.jpg

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