A Phase I, open-label, randomized, crossover study in healthy subjects to evaluate the bioavailability of, and the food effect on, a pomalidomide oral liquid suspension.

IF 3.1 Q2 PHARMACOLOGY & PHARMACY Clinical Pharmacology : Advances and Applications Pub Date : 2018-07-19 eCollection Date: 2018-01-01 DOI:10.2147/CPAA.S171735
Yan Li, Liangang Liu, Lian Huang, Xiaomin Wang, Matthew Hoffmann, Josephine Reyes, Maria Palmisano, Simon Zhou
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引用次数: 3

Abstract

Objective: The aim of this study was to evaluate the bioavailability of a pomalidomide oral liquid suspension relative to the commercial capsule formulation and to assess the food effect on the pomalidomide oral liquid suspension when administered as a single 4 mg dose.

Methods: This was an open-label, randomized, three-period, two-sequence crossover study in healthy subjects consisting of a screening phase, a baseline assessment phase, a treatment phase with three periods, and a follow-up phone call phase. Blood samples for pharmacokinetics (PK) assessment were collected up to 48 h postdose during each treatment period. Safety was evaluated throughout the study.

Results: Pomalidomide exposures were comparable in healthy subjects administered with a single oral 4 mg dose as the reference capsule or as the test liquid suspension formulations, demonstrated as the 90% confidence intervals of the geometric mean ratios for area under the plasma concentration-time curve calculated from time 0 to the last measurable concentration at time t (AUC0-t), area under the plasma concentration-time curve from time 0 to infinity (AUC0-∞), and peak (maximum) plasma drug concentration (Cmax) were completely contained within the bioequivalence range of 80-125%. Administration of the pomalidomide liquid suspension with a high fat meal resulted in a 3.0 h delay in pomalidomide time to Cmax (tmax) and an ~ 34.5% reduction in Cmax. However, the AUCs were comparable after dose administration with and without food.

Conclusion: A single oral dose of 4 mg of liquid suspension was bioequivalent to a single oral dose of 4 mg of capsule formulation. There was no clinically relevant impact of food on pomalidomide liquid suspension. Single oral doses of 4 mg pomalidomide were safe and well tolerated when administered as a liquid suspension under fed and fasted conditions or as a capsule under fasted conditions.

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一项在健康受试者中进行的I期、开放标签、随机、交叉研究,以评估泊马度胺口服液悬浮液的生物利用度和食物效应。
目的:本研究的目的是评估相对于商业胶囊制剂的泊马度胺口服液悬浮液的生物利用度,并评估单剂量4mg的泊马度胺口服液悬浮液的食用效应。方法:这是一项开放标签、随机、三期、两序列的健康受试者交叉研究,包括筛查阶段、基线评估阶段、三期治疗阶段和随访电话阶段。每次给药后48小时采集血样进行药代动力学(PK)评估。在整个研究过程中对安全性进行了评估。结果:健康受试者服用单次口服4 mg剂量的泊马度胺作为参考胶囊或试验液体悬浮液配方,其暴露可与从时间0到时间t最后可测浓度计算的血浆浓度-时间曲线下面积(AUC0-t)、从时间0到无穷远的血浆浓度-时间曲线下面积(AUC0-∞)的几何平均比值的90%置信区间相比较。峰(最大)血药浓度(Cmax)完全控制在80-125%的生物等效性范围内。在高脂餐中使用泊马度胺液体悬浮液,可使泊马度胺达到Cmax (tmax)的时间延迟3.0 h, Cmax降低34.5%。然而,在给药和不给药后,auc是相当的。结论:单次口服4mg液体悬浮液与单次口服4mg胶囊制剂具有生物等效性。食物对泊马度胺液体悬浮液没有临床相关的影响。单次口服4mg的泊马度胺在喂养和禁食条件下作为液体悬浮液或在禁食条件下作为胶囊使用是安全且耐受性良好的。
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来源期刊
CiteScore
4.60
自引率
0.00%
发文量
14
审稿时长
16 weeks
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