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支持雷特综合征患者使用托伐替丁的暴露-反应疗效建模。

Exposure-Response Efficacy Modeling to Support Trofinetide Dosing in Individuals with Rett Syndrome.

机构信息

Acadia Pharmaceuticals Inc., 12830 El Camino Real, Suite 400, San Diego, CA, 92130, USA.

Cognigen Corporation (a Simulations Plus Company), Buffalo, NY, USA.

出版信息

Adv Ther. 2024 Apr;41(4):1462-1480. doi: 10.1007/s12325-024-02796-y. Epub 2024 Feb 16.

Abstract

INTRODUCTION

Trofinetide was recently approved for the treatment of Rett syndrome (RTT) on the basis of the efficacy and safety findings of the phase 3 LAVENDER study, which used a body weight-based dosing regimen. Exposure-response (E-R) efficacy modeling was used to characterize relationships between trofinetide exposure measures (maximum drug concentration and area under the concentration-time curve for the dosing interval of 0-12 h [AUC]) and efficacy endpoints in RTT clinical studies to support the trofinetide dosing regimen.

METHODS

Efficacy endpoints were modeled using trofinetide exposure measures predicted from the population pharmacokinetic model and Bayesian estimates. The analysis population for each E-R model comprised individuals receiving placebo or trofinetide who had available trofinetide exposure measures. Efficacy endpoints were scores from the Rett Syndrome Behaviour Questionnaire (RSBQ), the Clinical Global Impression-Improvement, the Communication and Symbolic Behavior Scales Developmental Profile™ Infant-Toddler Checklist (CSBS-DP-IT) Social Composite, and the Rett Syndrome Clinician Rating of Ability to Communicate Choices (RTT-COMC).

RESULTS

Higher trofinetide exposure was associated with improvements in RSBQ, CSBS-DP-IT Social Composite, and RTT-COMC scores. Assuming target trofinetide AUC values of 800-1200 μg·h/mL, the reductions in RSBQ total scores at week 12 were approximately five- to seven-fold greater with trofinetide (range 3.55-4.94) versus placebo (0.76). Significant E-R relationships were also found for the CSBS-DP-IT Social Composite and RTT-COMC scores.

CONCLUSION

E-R efficacy modeling demonstrated significant relationships between trofinetide exposure and RSBQ, CSBS-DP-IT Social Composite, and RTT-COMC scores. Trofinetide is efficacious within the target exposure range, supporting the approved dosing regimen for trofinetide.

TRIAL REGISTRATION

NCT01703533, NCT02715115, NCT04181723.

摘要

简介

特立氟胺基于 3 期 LAVENDER 研究的疗效和安全性结果获得了雷特综合征(RTT)的批准,该研究采用了基于体重的给药方案。为了支持特立氟胺的给药方案,使用暴露-反应(E-R)疗效建模来描述 RTT 临床研究中特立氟胺暴露量(最大药物浓度和 0-12 小时给药间隔的浓度-时间曲线下面积[AUC])与疗效终点之间的关系。

方法

使用来自群体药代动力学模型和贝叶斯估计的特立氟胺暴露量来对疗效终点进行建模。每个 E-R 模型的分析人群包括接受安慰剂或特立氟胺治疗且具有特立氟胺暴露量的个体。疗效终点是雷特综合征行为问卷(RSBQ)、临床总体印象-改善、沟通与象征行为量表发展概况评定™婴儿-幼儿检查表(CSBS-DP-IT)社会综合评分和雷特综合征临床医生评定的沟通选择能力(RTT-COMC)的评分。

结果

较高的特立氟胺暴露量与 RSBQ、CSBS-DP-IT 社会综合评分和 RTT-COMC 评分的改善相关。假设目标特立氟胺 AUC 值为 800-1200μg·h/mL,特立氟胺(范围为 3.55-4.94)与安慰剂(0.76)相比,第 12 周的 RSBQ 总分降低约五到七倍。CSBS-DP-IT 社会综合评分和 RTT-COMC 评分也存在显著的 E-R 关系。

结论

E-R 疗效建模表明,特立氟胺暴露量与 RSBQ、CSBS-DP-IT 社会综合评分和 RTT-COMC 评分之间存在显著关系。特立氟胺在目标暴露范围内是有效的,支持特立氟胺的批准给药方案。

试验注册

NCT01703533、NCT02715115、NCT04181723。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ced/10960884/956bb88f59db/12325_2024_2796_Fig1_HTML.jpg

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