Early Clinical Development Research and Early Development Cardiovascular, Renal and Metabolism BioPharmaceuticals R&D AstraZeneca Gaithersburg MD.
Bioscience Research and Early Development Cardiovascular, Renal and Metabolism BioPharmaceuticals R&D AstraZeneca Gaithersburg MD.
J Am Heart Assoc. 2021 Jul 6;10(13):e014572. doi: 10.1161/JAHA.119.014572. Epub 2021 Jun 14.
Background MEDI6012 is recombinant human lecithin cholesterol acyltransferase, the rate-limiting enzyme in reverse cholesterol transport. Infusions of lecithin cholesterol acyltransferase have the potential to enhance reverse cholesterol transport and benefit patients with coronary heart disease. The purpose of this study was to test the safety, pharmacokinetic, and pharmacodynamic profile of MEDI6012. Methods and Results This phase 2a double-blind study randomized 48 subjects with stable coronary heart disease on a statin to a single dose of MEDI6012 or placebo (6:2) (NCT02601560) with ascending doses administered intravenously (24, 80, 240, and 800 mg) and subcutaneously (80 and 600 mg). MEDI6012 demonstrated rates of treatment-emergent adverse events that were similar to those of placebo. Dose-dependent increases in high-density lipoprotein cholesterol were observed with area under the concentration-time curves from 0 to 96 hours of 728, 1640, 3035, and 5318 should be: mg·h/mL in the intravenous dose groups and 422 and 2845 mg·h/mL in the subcutaneous dose groups. Peak mean high-density lipoprotein cholesterol percent change was 31.4%, 71.4%, 125%, and 177.8% in the intravenous dose groups and 18.3% and 111.2% in the subcutaneous dose groups, and was accompanied by increases in endogenous apoA1 (apolipoprotein A1) and non-ATP-binding cassette transporter A1 cholesterol efflux capacity. Decreases in apoB (apolipoprotein B) were observed across all dose levels and decreases in atherogenic small low-density lipoprotein particles by 41%, 88%, and 79% at the 80-, 240-, and 800-mg IV doses, respectively. Conclusions MEDI6012 demonstrated an acceptable safety profile and increased high-density lipoprotein cholesterol, endogenous apoA1, and non-ATP-binding cassette transporter A1 cholesterol efflux capacity while reducing the number of atherogenic low-density lipoprotein particles. These findings are supportive of enhanced reverse cholesterol transport and a functional high-density lipoprotein phenotype. Registration URL: https://www.clinicaltrials.gov; Unique identifier: NCT02601560.
MEDI6012 是重组人卵磷脂胆固醇酰基转移酶,是胆固醇逆转运的限速酶。卵磷脂胆固醇酰基转移酶输注可能增强胆固醇逆转运,有益于冠心病患者。本研究旨在检测 MEDI6012 的安全性、药代动力学和药效学特征。
这项 2a 期双盲研究将 48 例稳定型冠心病患者随机分为 MEDI6012 或安慰剂(6:2)组(NCT02601560),静脉内(24、80、240 和 800mg)和皮下(80 和 600mg)递增剂量给药。MEDI6012 治疗期间出现的不良事件发生率与安慰剂相似。观察到剂量依赖性的高密度脂蛋白胆固醇升高,静脉剂量组的 0 至 96 小时浓度-时间曲线下面积分别为 728、1640、3035 和 5318mg·h/mL,皮下剂量组分别为 422 和 2845mg·h/mL。静脉剂量组的高密度脂蛋白胆固醇平均峰值百分比变化分别为 31.4%、71.4%、125%和 177.8%,皮下剂量组分别为 18.3%和 111.2%,并伴有内源性载脂蛋白 A1(载脂蛋白 A1)和非 ATP 结合盒转运蛋白 A1 胆固醇流出能力增加。所有剂量水平均观察到载脂蛋白 B(载脂蛋白 B)降低,80、240 和 800mg 静脉剂量时小而致动脉粥样硬化的低密度脂蛋白颗粒分别降低 41%、88%和 79%。
MEDI6012 具有良好的安全性,可增加高密度脂蛋白胆固醇、内源性载脂蛋白 A1 和非 ATP 结合盒转运蛋白 A1 胆固醇流出能力,同时减少致动脉粥样硬化的低密度脂蛋白颗粒数量。这些发现支持增强胆固醇逆转运和具有功能的高密度脂蛋白表型。