Clinical Pharmacology and Pharmacometrics, AbbVie Inc., North Chicago, Illinois, USA.
Immunology Development, AbbVie Inc., North Chicago, Illinois, USA.
Clin Pharmacol Ther. 2020 Mar;107(3):639-649. doi: 10.1002/cpt.1668. Epub 2019 Nov 22.
Upadacitinib plasma concentrations, efficacy, and safety data from 216 subjects with moderate-to-severe active Crohn's disease (CD) from the 16-week induction period of the CELEST study were analyzed to characterize upadacitinib exposure-response relationships in CD. Subjects in CELEST received either placebo or upadacitinib (3, 6, 12, 24 mg b.i.d. or 24 mg q.d.). Exposure-response models were developed and utilized to simulate efficacy of induction doses of the immediate-release (IR) and extended-release (ER) formulations. Upadacitinib exposures associated with 18-24 mg b.i.d. (IR formulation) or 45-60 mg q.d. (ER formulation) are estimated to have greater efficacy during 12-week induction in patients with CD compared with lower doses. No exposure-response relations were observed with decreases in hemoglobin or lymphocytes at week 16 or with herpes zoster infections, pneumonia, or serious infections during 16 weeks of treatment in this study. These analyses informed the selection of upadacitinib induction dose for phase III studies in CD.
从 CELEST 研究的 16 周诱导期内 216 名中重度活动期克罗恩病(CD)患者的乌帕达替尼血浆浓度、疗效和安全性数据进行分析,以描述 CD 中乌帕达替尼的暴露-反应关系。CELEST 中的受试者接受安慰剂或乌帕达替尼(3、6、12、24mg 每日两次或 24mg 每日一次)。开发并利用暴露-反应模型来模拟即时释放(IR)和延长释放(ER)制剂诱导剂量的疗效。与较低剂量相比,在 CD 患者的 12 周诱导期内,估计 18-24mg 每日两次(IR 制剂)或 45-60mg 每日一次(ER 制剂)的乌帕达替尼暴露与更大的疗效相关。在这项研究中,在 16 周的治疗期间,第 16 周时血红蛋白或淋巴细胞减少、带状疱疹感染、肺炎或严重感染均未观察到与暴露相关的反应关系。这些分析为 CD 的 III 期研究中乌帕达替尼的诱导剂量选择提供了信息。