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在肝损伤患者中,小干扰 RNA 疗法 inclisiran 的药代动力学和药效学。

Pharmacokinetics and pharmacodynamics of inclisiran, a small interfering RNA therapy, in patients with hepatic impairment.

机构信息

Former employees of The Medicines Company, Europaallee 41, 8004 Zurich, Switzerland (Drs. Kallend and Wijngaard).

Novartis Pharmaceuticals Corporation, 1 Health Plaza, East Hanover, NJ 07936, USA (Dr. Stoekenbroek).

出版信息

J Clin Lipidol. 2022 Mar-Apr;16(2):208-219. doi: 10.1016/j.jacl.2022.01.001. Epub 2022 Jan 10.

Abstract

BACKGROUND

Inclisiran, a small interfering RNA molecule, reduces low-density lipoprotein cholesterol (LDL-C) by inhibiting production of proprotein convertase subtilisin/kexin type 9 (PCSK9) in the liver.

OBJECTIVE

To investigate the pharmacokinetics, pharmacodynamics, and safety of inclisiran in patients with mild or moderate hepatic impairment (HI) vs participants with normal hepatic function (NHF).

METHODS

In this single-center, open-label, parallel-group study, patients with mild (Child-Pugh A) or moderate (Child-Pugh B) HI and with NHF, matched by age, body mass index, sex, and race (if possible), received a single subcutaneous therapeutic dose of inclisiran (300 mg). Pharmacokinetic profiles, pharmacodynamic endpoints (PCSK9 and LDL-C), and safety were assessed.

RESULTS

Twenty-eight participants completed the study (mild HI: n = 10; moderate HI: n = 6; NHF: n = 12). Inclisiran achieved maximum plasma concentration at 4-6 h and was undetectable in plasma at 48 h in most participants, irrespective of liver function. Inclisiran exposure was 1.24-fold higher in the mild HI vs NHF groups (90% confidence interval [CI] 1.01-1.53) and 2.03-fold higher in the moderate HI vs NHF groups (90% CI 1.60-2.58). LDL-C and PCSK9 plasma levels decreased from baseline up to the last assessment on Day 60 in all groups, with a similar response in NHF and mild HI groups but a less pronounced and more varied decrease in the moderate HI group. Inclisiran was generally safe and well tolerated.

CONCLUSION

The pharmacokinetic exposure of inclisiran increased by up to two fold in patients with moderate HI compared with those with NHF, while pharmacodynamic effects remained relatively unchanged. Inclisiran is generally safe and well tolerated in patients with mild or moderate HI, with no dose adjustment needed. However, a larger, long-term clinical trial would help to further evaluate the long-term safety profile of inclisiran in patients with liver disease.

摘要

背景

Inclisiran 是一种小干扰 RNA 分子,通过抑制肝脏中前蛋白转化酶枯草溶菌素/柯萨奇蛋白酶 9(PCSK9)的产生来降低低密度脂蛋白胆固醇(LDL-C)。

目的

研究inclisiran 在轻度或中度肝损伤(HI)患者与肝功能正常(NHF)患者中的药代动力学、药效学和安全性。

方法

在这项单中心、开放标签、平行组研究中,年龄、体重指数、性别和种族(如果可能)相匹配的轻度(Child-Pugh A)或中度(Child-Pugh B)HI 患者和 NHF 患者接受了单次皮下治疗剂量的 inclisiran(300mg)。评估了药代动力学特征、药效学终点(PCSK9 和 LDL-C)和安全性。

结果

28 名参与者完成了研究(轻度 HI:n=10;中度 HI:n=6;NHF:n=12)。在大多数参与者中,inclisiran 在 4-6 小时达到最大血浆浓度,在 48 小时时在血浆中无法检测到,无论肝功能如何。轻度 HI 组与 NHF 组相比,inclisiran 暴露量增加了 1.24 倍(90%置信区间 [CI]1.01-1.53),中度 HI 组与 NHF 组相比,增加了 2.03 倍(90%CI1.60-2.58)。所有组的 LDL-C 和 PCSK9 血浆水平从基线开始下降,直至第 60 天的最后一次评估,NHF 和轻度 HI 组的反应相似,但中度 HI 组的下降幅度较小且变化较大。inclisiran 通常是安全且耐受良好的。

结论

与 NHF 患者相比,中度 HI 患者的 inclisiran 药代动力学暴露量增加了 1 到 2 倍,而药效学作用相对不变。在轻度或中度 HI 患者中,inclisiran 通常是安全且耐受良好的,无需调整剂量。然而,更大规模的长期临床试验将有助于进一步评估inclisiran 在肝病患者中的长期安全性。

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