Ionis Pharmaceuticals, Carlsbad, CA, USA.
Novartis Pharma AG, Basel, Switzerland.
Lipids Health Dis. 2024 Oct 3;23(1):329. doi: 10.1186/s12944-024-02297-5.
Olezarsen is a GalNAc-conjugated, hepatic-targeted antisense oligonucleotide that lowers apolipoprotein C-III (apoC-III) and triglyceride levels. The efficacy and safety of olezarsen has not previously been studied in ethnically diverse American populations. The aim of this study is to assess the effect of olezarsen in healthy Japanese Americans.
A randomized, placebo-controlled, double-blind phase 1 study was performed in 28 healthy Japanese American participants treated with olezarsen in single-ascending doses (SAD; 30, 60, 90 mg) or multiple doses (MD; 60 mg every 4 weeks for 4 doses). The primary, secondary, and exploratory objectives were safety and tolerability, pharmacokinetics, and effects of olezarsen on fasting serum triglycerides and apoC-III, respectively.
There were 20 participants (16 active:4 placebo) in the SAD part of the study, and 8 participants (6 active:2 placebo) in the MD part of the study. For the primary endpoint, no serious adverse events or clinically relevant laboratory abnormalities were reported. The majority of olezarsen plasma exposure occurred within 24 h post-dose. In the SAD cohorts at Day 15 the percentage reduction in apoC-III/TG was - 39.4%/ - 17.8%, - 60.8%/ - 52.7%, and - 68.1%/ - 39.2% in the 30, 60 and 90 mg doses, respectively, vs 2.3%/44.5% increases in placebo. In the MD cohort, at Day 92 the percentage reduction in apoC-III/TG was - 81.6/ - 73.8% vs - 17.2/ - 40.8% reduction in placebo. Favorable changes were also present in VLDL-C, apoB and HDL-C.
Single- and multiple-dose administration of olezarsen was safe, was well tolerated, and significantly reduced apoC-III and triglyceride levels in healthy Japanese Americans.
Olezarsen 是一种 GalNAc 缀合的、靶向肝脏的反义寡核苷酸,可降低载脂蛋白 C-III(apoC-III)和甘油三酯水平。Olezarsen 的疗效和安全性此前尚未在种族多样化的美国人群中进行研究。本研究旨在评估 olezarsen 在健康的日本裔美国人中的效果。
在 28 名健康的日本裔美国人参与者中进行了一项随机、安慰剂对照、双盲的 1 期研究,他们接受了单剂量递增(SAD;30、60、90mg)或多剂量(MD;60mg 每 4 周一次,共 4 次)的 olezarsen 治疗。主要、次要和探索性目标分别是安全性和耐受性、药代动力学以及 olezarsen 对空腹血清甘油三酯和 apoC-III 的影响。
在研究的 SAD 部分有 20 名参与者(16 名活性:4 名安慰剂),在 MD 部分有 8 名参与者(6 名活性:2 名安慰剂)。对于主要终点,没有报告严重不良事件或临床相关的实验室异常。大多数 olezarsen 血浆暴露发生在给药后 24 小时内。在 SAD 队列中,在第 15 天,apoC-III/TG 的百分比降低分别为-39.4%/-17.8%、-60.8%/-52.7%和-68.1%/-39.2%,而安慰剂组分别为 2.3%/44.5%的增加。在 MD 队列中,在第 92 天,apoC-III/TG 的百分比降低分别为-81.6%/-73.8%,而安慰剂组分别为-17.2%/-40.8%。VLDL-C、apoB 和 HDL-C 也出现了有利的变化。
在健康的日本裔美国人中,单次和多次给药 olezarsen 是安全的,耐受性良好,可显著降低 apoC-III 和甘油三酯水平。