A Randomized, Open-Label, Phase I, Single-Dose Study of Antisense Oligonucleotide, Vupanorsen, in Chinese Adults with Elevated Triglycerides.

IF 2.2 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Drugs in Research & Development Pub Date : 2024-06-01 Epub Date: 2024-07-01 DOI:10.1007/s40268-024-00467-5
Xiaojie Wu, Jicheng Yu, Beikang Ge, Jeffrey Wang, Xiaoran Han, Chunye Zhang, Xiaomeng Mao, Hindu Kalluru, Candace Bramson, Steven G Terra, Jing Liu
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引用次数: 0

Abstract

Background: Vupanorsen is a GalNAc3-conjugated antisense oligonucleotide targeting angiopoietin-like 3 (ANGPTL3) mRNA shown to reduce atherogenic lipoproteins in individuals with dyslipidemia.

Objectives: The aim of this study was to satisfy Chinese regulatory requirements and support ethnic sensitivity assessment by evaluating pharmacokinetics (PK), pharmacodynamics (PD), and safety of vupanorsen in healthy Chinese adults with elevated triglycerides (TG).

Methods: In this phase I, parallel-cohort, open-label study, 18 Chinese adults with elevated fasting TG (≥ 90 mg/dL) were randomized 1:1 to receive a single subcutaneous dose of vupanorsen 80 mg or 160 mg. PK parameters, PD markers (including ANGPTL3, TG, non-high-density lipoprotein cholesterol [non-HDL-C]), and safety were assessed.

Results: Absorption of vupanorsen was rapid (median time to maximum concentration [Tmax]: 2.0 h for both doses), followed by a multiphasic decline (mean terminal half-life 475.9 [80 mg] and 465.2 h [160 mg]). Exposure (area under curve [AUC] and maximum plasma concentration [Cmax]) generally increased in a greater than dose-proportional manner from 80 mg to 160 mg. Time-dependent reductions in ANGPTL3 and lipid parameters were observed. Mean percentage change from baseline for the 80-mg and 160-mg doses, respectively, were - 59.7% and - 69.5% for ANGPTL3, - 41.9% and - 52.5% for TG, and - 23.2% and - 25.4% for non-HDL-C. No serious or severe adverse events (AEs), deaths, or discontinuations due to AEs were reported. Three participants experienced treatment-related AEs; all were mild and resolved by end of study.

Conclusions: This study provided the first clinical vupanorsen data in China. In Chinese participants with elevated TG, PK and PD parameters were consistent with those reported previously in non-Chinese participants, including in Japanese individuals. No safety concerns were noted.

Trial registration: ClinicalTrials.gov identifier: NCT04916795.

Abstract Image

反义寡核苷酸 Vupanorsen 在甘油三酯升高的中国成人中的随机、开放标签、I 期、单剂量研究。
背景:武帕诺森是一种以血管生成素样 3 (ANGPTL3) mRNA 为靶点的 GalNAc3 结合物反义寡核苷酸,被证明可降低血脂异常患者的致动脉粥样脂蛋白:本研究旨在通过评估武帕诺森在甘油三酯(TG)升高的中国健康成人中的药代动力学(PK)、药效学(PD)和安全性,满足中国法规要求并支持种族敏感性评估:在这项 I 期平行队列开放标签研究中,18 名空腹甘油三酯(TG)升高(≥ 90 mg/dL)的中国成年人按 1:1 随机分配接受单剂量皮下注射武潘诺森 80 毫克或 160 毫克。对PK参数、PD指标(包括ANGPTL3、TG、非高密度脂蛋白胆固醇[non-HDL-C])和安全性进行了评估:武帕诺森的吸收速度很快(两种剂量达到最大浓度[Tmax]的中位时间:2.0小时),随后出现多相下降(平均终末半衰期分别为475.9小时[80毫克]和465.2小时[160毫克])。从80毫克到160毫克,暴露量(曲线下面积[AUC]和最大血浆浓度[Cmax])的增加幅度一般大于剂量比例。观察到 ANGPTL3 和血脂参数的降低具有时间依赖性。与基线相比,80 毫克和 160 毫克剂量的平均百分比变化分别为:ANGPTL3 - 59.7% 和 - 69.5%;TG - 41.9% 和 - 52.5%;非 HDL-C - 23.2% 和 - 25.4%。没有严重或严重不良事件 (AE)、死亡或因 AE 而停药的报告。三名参与者出现了与治疗相关的不良反应,但均为轻微不良反应,并在研究结束时得到缓解:这项研究为中国提供了首个武帕诺森临床数据。在TG升高的中国参与者中,PK和PD参数与之前报道的非中国参与者(包括日本人)的参数一致。未发现任何安全性问题:试验注册:ClinicalTrials.gov identifier:NCT04916795.
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来源期刊
Drugs in Research & Development
Drugs in Research & Development Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
5.10
自引率
0.00%
发文量
31
审稿时长
8 weeks
期刊介绍: Drugs in R&D is an international, peer reviewed, open access, online only journal, and provides timely information from all phases of drug research and development that will inform clinical practice. Healthcare decision makers are thus provided with knowledge about the developing place of a drug in therapy. The Journal includes: Clinical research on new and established drugs; Preclinical research of direct relevance to clinical drug development; Short communications and case study reports that meet the above criteria will also be considered; Reviews may also be considered.
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