Shoji S, Suzuki A, Conrado D J, Peterson M C, Hey-Hadavi J, McCabe D, Rojo R, Tammara B K
Pfizer Japan Inc, Tokyo, Japan.
Pfizer Inc, Groton, Connecticut, USA.
CPT Pharmacometrics Syst Pharmacol. 2017 Jul;6(7):439-448. doi: 10.1002/psp4.12201. Epub 2017 May 27.
Fosdagrocorat (PF-04171327), a dissociated agonist of the glucocorticoid receptor, has potent anti-inflammatory activity in patients with rheumatoid arthritis with reduced adverse effects on bone health. To identify fosdagrocorat doses with bone formation marker changes similar to prednisone 5 mg, we characterized treatment-related changes in amino-terminal propeptide of type I collagen (P1NP) and osteocalcin (OC) with fosdagrocorat (1, 5, 10, or 15 mg) and prednisone (5 or 10 mg) in a phase II randomized trial (N = 323). The time course of markers utilized a mixed-effects longitudinal kinetic-pharmacodynamic model. Median predicted changes from baseline at week 8 with fosdagrocorat 5, 10, and 15 mg were -18, -22, and -22% (P1NP), and -7, -13, and -17% (OC), respectively. Changes with prednisone 5 and 10 mg were -15% and -18% (P1NP) and -10% and -17% (OC). The probability of fosdagrocorat doses up to 15 mg being noninferior to prednisone 5 mg for P1NP and OC changes was >90%.
福斯可罗卡特(PF-04171327)是一种糖皮质激素受体解离激动剂,在类风湿性关节炎患者中具有强大的抗炎活性,且对骨骼健康的不良影响较小。为了确定与5毫克泼尼松具有相似骨形成标志物变化的福斯可罗卡特剂量,我们在一项II期随机试验(N = 323)中,对福斯可罗卡特(1、5、10或15毫克)和泼尼松(5或10毫克)治疗相关的I型胶原氨基端前肽(P1NP)和骨钙素(OC)变化进行了特征分析。标志物的时间进程采用了混合效应纵向动力学-药效学模型。福斯可罗卡特5、10和15毫克在第8周时相对于基线的预测变化中位数分别为-18%、-22%和-22%(P1NP),以及-7%、-13%和-17%(OC)。5毫克和10毫克泼尼松的变化分别为-15%和-18%(P1NP)以及-10%和-17%(OC)。对于P1NP和OC的变化,高达15毫克的福斯可罗卡特剂量不劣于5毫克泼尼松的概率>90%。