Youssef Amir S, Ismail Mohamed, Han Kelong, Magee Mindy, Nader Ahmed
Clinical Pharmacology Modeling and Simulation, GSK, Collegeville, PA, USA.
Enhanced Pharmacodynamics LLC, Buffalo, NY, USA.
Infect Dis Ther. 2024 Jul;13(7):1515-1530. doi: 10.1007/s40121-024-00980-9. Epub 2024 May 25.
Bepirovirsen is a novel antisense oligonucleotide in development for chronic hepatitis B virus (HBV) infection therapy. Understanding the impact that clinical characteristics may have on bepirovirsen exposure is important for determining efficacious and well-tolerated dosing regimens. This analysis evaluated demographics and clinical characteristics associated with bepirovirsen exposure using a population pharmacokinetic (PK) analysis.
Population PK analyses were conducted using pooled data from three phase 1/2 clinical studies (NCT03020745/NCT02981602/NCT04449029) to construct a structural PK model for bepirovirsen that adequately described plasma concentration-time profiles and identify covariates that affect systemic exposure. The final population PK model was used to simulate bepirovirsen exposure measures to inform exposures at different dose levels and within different subpopulations.
Bepirovirsen PK data were well-described by a linear, three-compartment model with first-order absorption and absorption delay. Chronic HBV infection status, body weight, and Asian versus non-Asian race were key covariates included in the final model. Visual inspection of correlation scatter plots confirmed general agreement between observed and predicted data from the studies. In simulations, bepirovirsen systemic exposure was dosed proportionally and predicted to be almost completely washed out by 12 weeks following the final 300-mg dose. Differences in body weight, Asian race, or disease status did not result in clinically relevant differences in exposure.
This analysis demonstrated that the linear three-compartmental model accurately described bepirovirsen PK data. The lack of clinically relevant differences seen in exposure indicate that dose adjustments are not recommended for bepirovirsen based on demographics or clinical characteristics.
贝派罗韦生是一种正在开发用于治疗慢性乙型肝炎病毒(HBV)感染的新型反义寡核苷酸。了解临床特征对贝派罗韦生暴露量的影响对于确定有效且耐受性良好的给药方案很重要。本分析使用群体药代动力学(PK)分析评估了与贝派罗韦生暴露相关的人口统计学和临床特征。
使用来自三项1/2期临床研究(NCT03020745/NCT02981602/NCT04449029)的汇总数据进行群体PK分析,以构建能充分描述贝派罗韦生血浆浓度-时间曲线的结构PK模型,并识别影响全身暴露的协变量。最终的群体PK模型用于模拟贝派罗韦生暴露量测量,以了解不同剂量水平和不同亚组中的暴露情况。
贝派罗韦生的PK数据通过具有一级吸收和吸收延迟的线性三室模型得到了很好的描述。慢性HBV感染状态、体重以及亚洲与非亚洲种族是最终模型中包含的关键协变量。对相关性散点图的直观检查证实了研究中观察到的数据与预测数据之间的总体一致性。在模拟中,贝派罗韦生的全身暴露量按比例给药,预计在最后一次300毫克剂量后的12周内几乎完全清除。体重、亚洲种族或疾病状态的差异并未导致暴露量出现临床相关差异。
本分析表明线性三室模型准确描述了贝派罗韦生的PK数据。暴露量方面未观察到临床相关差异,这表明不建议根据人口统计学或临床特征对贝派罗韦生进行剂量调整。