Targeting the angiopoietin-like protein 3/8 complex with a monoclonal antibody in patients with mixed hyperlipidemia: a phase 1 trial

IF 58.7 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Daniel Gaudet, Malgorzata Gonciarz, Xi Shen, Jennifer K. Leohr, Thomas P. Beyer, Jonathan W. Day, Garrett R. Mullins, Eugene Y. Zhen, Maryalice Hartley, Miriam Larouche, Robert J. Konrad, Olivier Benichou, Giacomo Ruotolo
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Abstract

The angiopoietin-like protein 3/8 complex (ANGPTL3/8) inhibits lipoprotein lipase (LPL) activity, primarily in oxidative tissues, and does so more potently than ANGPTL3, making ANPTL3/8 an attractive target for treating dyslipidemia. This study enrolled 48 adults (36 men, 12 women) with mixed hyperlipidemia to assess the primary outcome of safety and the secondary outcomes of pharmacokinetics and pharmacodynamics of ascending doses of LY3475766, a human monoclonal antibody that specifically blocks ANGPTL3/8-mediated inhibition of LPL activity. Participants received a single dose of LY3475766 or placebo. LY3475766 was well tolerated with no severe adverse events or adverse event-related discontinuations. Compared with placebo, LY3475766 dose-dependently reduced the concentration of triglycerides (−70%), remnant cholesterol (−86%), low-density lipoprotein cholesterol (−32%), non-high-density lipoprotein cholesterol (non-HDL-C) (−35%) and apolipoprotein B (−29%) while increasing HDL-C (+27%). LY3475766 thus significantly reduced atherogenic lipoprotein levels while increasing HDL-C levels; however, the effects on cardiovascular risk remain to be established. ClinicalTrials.gov registration: NCT04052594.

Abstract Image

针对混合高脂血症患者的血管生成素样蛋白3/8复合物的单克隆抗体:一项1期试验
血管生成素样蛋白3/8复合物(ANGPTL3/8)主要在氧化组织中抑制脂蛋白脂肪酶(LPL)活性,并且比ANGPTL3更有效,使ANPTL3/8成为治疗血脂异常的有吸引力的靶点。该研究招募了48名患有混合性高脂血症的成年人(36名男性,12名女性),以评估增加剂量LY3475766的主要安全性结果,以及药代动力学和药效学的次要结果。LY3475766是一种特异性阻断angptl3 /8介导的LPL活性抑制的人单克隆抗体。参与者接受单剂量LY3475766或安慰剂。LY3475766耐受性良好,无严重不良事件或不良事件相关停药。与安慰剂相比,LY3475766剂量依赖性地降低了甘油三酯(- 70%)、残余胆固醇(- 86%)、低密度脂蛋白胆固醇(- 32%)、非高密度脂蛋白胆固醇(非HDL-C)(- 35%)和载脂蛋白B(- 29%)的浓度,同时增加了HDL-C(+27%)。LY3475766因此显著降低致动脉粥样硬化脂蛋白水平,同时增加HDL-C水平;然而,对心血管风险的影响仍有待确定。ClinicalTrials.gov注册:NCT04052594。
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来源期刊
Nature Medicine
Nature Medicine 医学-生化与分子生物学
CiteScore
100.90
自引率
0.70%
发文量
525
审稿时长
1 months
期刊介绍: Nature Medicine is a monthly journal publishing original peer-reviewed research in all areas of medicine. The publication focuses on originality, timeliness, interdisciplinary interest, and the impact on improving human health. In addition to research articles, Nature Medicine also publishes commissioned content such as News, Reviews, and Perspectives. This content aims to provide context for the latest advances in translational and clinical research, reaching a wide audience of M.D. and Ph.D. readers. All editorial decisions for the journal are made by a team of full-time professional editors. Nature Medicine consider all types of clinical research, including: -Case-reports and small case series -Clinical trials, whether phase 1, 2, 3 or 4 -Observational studies -Meta-analyses -Biomarker studies -Public and global health studies Nature Medicine is also committed to facilitating communication between translational and clinical researchers. As such, we consider “hybrid” studies with preclinical and translational findings reported alongside data from clinical studies.
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