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在健康受试者中,奥美拉唑与奈非那韦合用时,奈非那韦的全身暴露量显著降低。

Significant decrease in nelfinavir systemic exposure after omeprazole coadministration in healthy subjects.

作者信息

Fang Annie F, Damle Bharat D, LaBadie Robert R, Crownover Penelope H, Hewlett Dial, Glue Paul W

机构信息

Pfizer Inc., New York, New York, USA.

出版信息

Pharmacotherapy. 2008 Jan;28(1):42-50. doi: 10.1592/phco.28.1.42.

Abstract

STUDY OBJECTIVES

To assess the effect of omeprazole on the multiple-dose (steady-state) pharmacokinetics and safety of nelfinavir, and to evaluate the safety and tolerability of nelfinavir when administered alone and with omeprazole.

DESIGN

Open-label, two-period, single-fixed-sequence study.

SETTING

Clinical research unit of a large, teaching hospital.

PARTICIPANTS

Twenty healthy volunteers (mean age 26 +/- 9 yrs, range 18-48 yrs). Intervention. Subjects received nelfinavir 1250 mg every 12 hours for 4 days (period 1). After a 7-day washout period, subjects were coadministered nelfinavir 1250 mg every 12 hours and omeprazole 40 mg every 24 hours for 4 days (period 2).

MEASUREMENTS AND MAIN RESULTS

The pharmacokinetics of nelfinavir and its active metabolite M8 were determined on day 4 of both periods. Plasma samples were assayed by a high-performance liquid chromatography-ultraviolet method for nelfinavir and M8 concentrations, and noncompartmental pharmacokinetic analysis was performed by using analytical software. In the presence of omeprazole, nelfinavir area under the concentration-time curve over the dosing interval (AUC(tau)), maximum observed plasma concentration (C(max)), and minimum observed plasma concentration (C(min)) were reduced by an average of 36%, 37%, and 39%, respectively, relative to administration of nelfinavir alone. The AUC(tau), C(max), and C(min) of M8 were reduced by an average of 92%, 89%, and 75%, respectively. The slopes of the terminal elimination phase of nelfinavir and M8 plasma concentration-time curves were similar between treatments. Nelfinavir was well tolerated when administered alone and when coadministered with omeprazole.

CONCLUSION

The observed reduction in the systemic exposure to both nelfinavir and its active metabolite M8 after coadministration with omeprazole could result in loss of virologic control and potential emergence of drug resistance. Hence, omeprazole should not be coadministered to patients taking nelfinavir.

摘要

研究目的

评估奥美拉唑对奈非那韦多剂量(稳态)药代动力学及安全性的影响,并评价奈非那韦单独使用及与奥美拉唑合用时的安全性和耐受性。

设计

开放标签、两阶段、单固定序列研究。

地点

一家大型教学医院的临床研究单位。

参与者

20名健康志愿者(平均年龄26±9岁,范围18 - 48岁)。干预措施:受试者在第1阶段每12小时接受1250 mg奈非那韦,共4天。经过7天的洗脱期后,在第2阶段受试者每12小时接受1250 mg奈非那韦并每24小时接受40 mg奥美拉唑,共治疗4天。

测量指标及主要结果

在两个阶段的第4天测定奈非那韦及其活性代谢产物M8的药代动力学。采用高效液相色谱 - 紫外法测定血浆样本中奈非那韦和M8的浓度,并使用分析软件进行非房室药代动力学分析。与单独使用奈非那韦相比,在合用奥美拉唑的情况下,奈非那韦在给药间隔内的浓度 - 时间曲线下面积(AUC(tau))、观察到的最大血浆浓度(C(max))和观察到的最小血浆浓度(C(min))分别平均降低了36%、37%和39%。M8的AUC(tau)、C(max)和C(min)分别平均降低了92%、89%和75%。各治疗组间奈非那韦和M8血浆浓度 - 时间曲线的末端消除相斜率相似。奈非那韦单独使用及与奥美拉唑合用时耐受性良好。

结论

与奥美拉唑合用时,观察到奈非那韦及其活性代谢产物M8的全身暴露量降低,这可能导致病毒学控制丧失和耐药性的潜在出现。因此,服用奈非那韦的患者不应合用奥美拉唑。

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