Population Pharmacokinetics and Dosing Simulations for Paliperidone Palmitate 351 mg as Alternative Maintenance Doses in Patients With Schizophrenia or Schizoaffective Disorder.

IF 4.2 2区 医学 Q1 PSYCHIATRY
Yonglin Chen, Leijun Hu, Jonathan M Meyer, Leslie Citrome, Hongtao Song, Siwen Wang, Pinglan Liu, John J Yang, Ying Dong
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引用次数: 0

Abstract

Objective: Once-monthly paliperidone palmitate (PP1M) extended-release injectable suspension is approved for the treatment of adults with schizophrenia or schizoaffective disorder. A 351 mg dose of PP1M (LY03010 [brand name Erzofri]) became available in the US in April 2025 and is approved as a single initiation injection followed by recommended monthly maintenance doses up to 234 mg. The objective of this study was to investigate steady-state paliperidone exposure following administration of 351 mg as a maintenance dose at different dosing intervals using population pharmacokinetic (popPK) analysis.

Methods: A popPK model was developed using Nonlinear Mixed Effects Modeling (NONMEM) based on the paliperidone concentration data from 2 phase 1 studies for LY03010. Plasma paliperidone exposures based on model simulations were summarized.

Results: Simulated plasma concentration-time profiles demonstrated that LY03010 351 mg every 4 weeks (Q4W) produced steady-state paliperidone exposure comparable to 234 mg every 3 weeks (Q3W) based on analysis of Cmax,ss and Ctrough,ss. Simulated data indicated that administration of LY03010 351 mg every 6 weeks (Q6W) provided similar paliperidone exposure to 234 mg PP1M Q4W at steady state. Simulation of LY03010 351 mg every 8 weeks (Q8W) showed that Cmax,ss of paliperidone fell in-between that of 234 mg Q4W and 156 mg Q4W while Ctrough,ss was comparable to that of 117 mg Q4W.

Conclusions: PopPK simulations suggest that LY03010 351 mg may provide alternative treatment options as a maintenance dose at different dosing intervals. Currently, there are no clinical data to support the alternative dosing regimens.

Trial Registration: ClinicalTrials.gov identifiers: NCT04572685 and NCT04922593.

棕榈酸帕利哌酮351 mg作为精神分裂症或分裂情感性障碍患者替代维持剂量的人群药代动力学和剂量模拟
目的:每月一次的棕榈酸帕利哌酮(PP1M)缓释注射混悬液被批准用于治疗成人精神分裂症或分裂情感性障碍。351 mg剂量的PP1M (LY03010[品牌Erzofri])于2025年4月在美国上市,并被批准作为单次起始注射,随后推荐每月维持剂量高达234 mg。本研究的目的是利用群体药代动力学(popPK)分析,研究在不同给药间隔给药351 mg作为维持剂量后的稳态帕利哌酮暴露。方法:采用非线性混合效应模型(NONMEM),以LY03010的2个一期研究的帕利哌酮浓度数据为基础,建立popPK模型。总结了基于模型模拟的血浆帕利哌酮暴露。结果:模拟血浆浓度-时间曲线显示,基于Cmax,ss和cough,ss的分析,LY03010 351 mg每4周(Q4W)产生的稳态帕利哌酮暴露与234 mg每3周(Q3W)相当。模拟数据表明,每6周给药LY03010 351 mg (Q6W)在稳定状态下提供与234 mg PP1M Q4W相似的帕立酮暴露。LY03010 351 mg每8周(Q8W)的模拟显示,帕利哌酮的Cmax,ss介于234 mg Q4W和156 mg Q4W之间,而Cmax,ss与117 mg Q4W相当。结论:PopPK模拟表明,LY03010 351 mg可以作为不同给药间隔的维持剂量提供替代治疗选择。目前,没有临床数据支持替代给药方案。试验注册:ClinicalTrials.gov标识符:NCT04572685和NCT04922593。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Clinical Psychiatry
Journal of Clinical Psychiatry 医学-精神病学
CiteScore
7.40
自引率
1.90%
发文量
0
审稿时长
3-8 weeks
期刊介绍: For over 75 years, The Journal of Clinical Psychiatry has been a leading source of peer-reviewed articles offering the latest information on mental health topics to psychiatrists and other medical professionals.The Journal of Clinical Psychiatry is the leading psychiatric resource for clinical information and covers disorders including depression, bipolar disorder, schizophrenia, anxiety, addiction, posttraumatic stress disorder, and attention-deficit/hyperactivity disorder while exploring the newest advances in diagnosis and treatment.
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