首页> 美国卫生研究院文献>Springer Open Choice >Population Pharmacokinetic Analysis and Model-Based Simulations of Aripiprazole for a 1-Day Initiation Regimen for the Long-Acting Antipsychotic Aripiprazole Lauroxil
【2h】

Population Pharmacokinetic Analysis and Model-Based Simulations of Aripiprazole for a 1-Day Initiation Regimen for the Long-Acting Antipsychotic Aripiprazole Lauroxil

机译:长效抗精神病药物阿立哌唑月桂醇的1天启动方案阿立哌唑的群体药代动力学分析和基于模型的模拟

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Background and ObjectivesAripiprazole lauroxil (AL), a long-acting injectable antipsychotic for the treatment of schizophrenia, requires 21 days of oral aripiprazole supplementation upon initiation (21-day initiation regimen). An alternative 1-day initiation regimen utilizing a nano-crystalline milled dispersion of AL (ALNCD) plus a single 30 mg oral aripiprazole dose achieved aripiprazole concentrations associated with therapeutic doses of aripiprazole in the same time frame as the 21-day initiation regimen when starting AL (441 or 882 mg). A population pharmacokinetic (PopPK) model was developed to describe aripiprazole pharmacokinetics following administration of ALNCD, AL and oral aripiprazole, and evaluate dosing scenarios likely to be encountered in clinical practice.
机译:背景与目的阿立哌唑月桂酯(AL)是一种用于精神分裂症的长效注射抗精神病药,在开始使用时需要21天口服阿立哌唑补充剂(21天开始治疗方案)。在开始使用21天起始方案的同一时间范围内,另一种利用纳米晶体研磨的AL(ALNCD)研磨分散液加上30 mg口服阿立哌唑的替代方案达到了阿立哌唑浓度与阿立哌唑治疗剂量的相关剂量AL(441或882毫克)。开发了一种群体药代动力学(PopPK)模型来描述阿立哌唑在ALNCD,AL和口服阿立哌唑给药后的药代动力学,并评估临床实践中可能遇到的给药方案。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号