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两种长效注射用阿立哌唑制剂给药后的血浆浓度:间接比较(2个月疗程)

Aripiprazole Plasma Concentrations Delivered from Two 2-Month Long-Acting Injectable Formulations: An Indirect Comparison.

作者信息

Harlin Matthew, Chepke Craig, Larsen Frank, Bell Lynum Karimah S, Chumki Sanjeda R, Fitzgerald Heather, Such Pedro, Madera-McDonough Jessica, Yildirim Murat, Panni Moeen, Saklad Stephen R

机构信息

Quantitative Pharmacology, Clinical Pharmacology, Early Phase & Translational Medicine, Otsuka Pharmaceutical Development & Commercialization Inc., Princeton, NJ, USA.

Department of Psychiatry, University of North Carolina School of Medicine, Chapel Hill, NC, USA.

出版信息

Neuropsychiatr Dis Treat. 2023 Jun 8;19:1409-1416. doi: 10.2147/NDT.S412357. eCollection 2023.

Abstract

Aripiprazole 2-month ready-to-use 960 mg (Ari 2MRTU 960) is a novel long-acting injectable (LAI) formulation of aripiprazole monohydrate for administration once every 2 months, developed for the treatment of schizophrenia or maintenance monotherapy treatment of bipolar I disorder in adults (indication will vary by country). Aripiprazole lauroxil 1064 mg (AL 1064) is an LAI formulation of aripiprazole lauroxil, an aripiprazole prodrug, for administration once every 2 months, indicated for the treatment of schizophrenia in adults. This analysis provides an indirect comparison of aripiprazole plasma concentrations following multiple doses of either formulation. Clinical trial data were used to determine average steady-state aripiprazole plasma concentration (C), maximum aripiprazole plasma concentration (C), and other pharmacokinetic parameters of either formulation following four administrations (96 patients received Ari 2MRTU 960; 28 patients received AL 1064). All pharmacokinetic parameters were considered in the context of a minimum aripiprazole therapeutic concentration (C) of ≥95 ng/mL. An exposure-response analysis using data from two Phase III trials of aripiprazole once-monthly (an aripiprazole monohydrate LAI, administered monthly), showed that patients with a C ≥95 ng/mL are 4.41 times less likely to relapse than patients with a C <95 ng/mL. A similar analysis has not been performed for AL 1064. However, consensus guidelines for therapeutic drug monitoring recommend a range of 100-350 ng/mL for aripiprazole. Following four administrations, mean (standard deviation [SD]) C over the 2-month dosing interval was 263 (133) ng/mL for Ari 2MRTU 960 and 140.7 (57.3) ng/mL for AL 1064. Mean (SD) C during the fourth dosing interval was 342 (157) ng/mL for Ari 2MRTU 960 and 188.8 (79.8) ng/mL for AL 1064. This indirect comparison showed that, following four administrations, Ari 2MRTU 960 and AL 1064 delivered mean aripiprazole plasma concentrations that remained above the minimum therapeutic concentration of aripiprazole over the 2-month dosing interval.

摘要

阿立哌唑2个月即用型960毫克制剂(阿立哌唑2MRTU 960)是一种新型的阿立哌唑一水合物长效注射剂(LAI),每2个月给药一次,用于治疗成人精神分裂症或双相I型障碍的维持单药治疗(适应症因国家而异)。阿立哌唑月桂酸酯1064毫克制剂(AL 1064)是阿立哌唑月桂酸酯(一种阿立哌唑前药)的LAI制剂,每2个月给药一次,用于治疗成人精神分裂症。本分析对两种制剂多次给药后的阿立哌唑血浆浓度进行了间接比较。临床试验数据用于确定两种制剂在四次给药后(96例患者接受阿立哌唑2MRTU 960;28例患者接受AL 1064)的平均稳态阿立哌唑血浆浓度(C)、最大阿立哌唑血浆浓度(C)和其他药代动力学参数。所有药代动力学参数均在阿立哌唑最低治疗浓度(C)≥95纳克/毫升的背景下进行考虑。一项使用阿立哌唑每月一次(一种阿立哌唑一水合物LAI,每月给药)的两项III期试验数据进行的暴露-反应分析表明,C≥95纳克/毫升的患者复发可能性比C<95纳克/毫升的患者低4.41倍。尚未对AL 1064进行类似分析。然而,治疗药物监测的共识指南建议阿立哌唑的范围为100-350纳克/毫升。四次给药后,阿立哌唑2MRTU 960在2个月给药间隔内的平均(标准差[SD])C为263(133)纳克/毫升,AL 1064为140.7(57.3)纳克/毫升。第四次给药间隔期间,阿立哌唑2MRTU 960的平均(SD)C为342(157)纳克/毫升,AL 1064为188.8(79.8)纳克/毫升。这种间接比较表明,四次给药后,阿立哌唑2MRTU 960和AL 1064在2个月给药间隔内的平均阿立哌唑血浆浓度均保持在阿立哌唑最低治疗浓度以上。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deaa/10259522/0537927c8edd/NDT-19-1409-g0001.jpg

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