首页> 外文期刊>Diabetic medicine: A journal of the British Diabetic Association >Prophylactic use of anti-emetic medications reduced nausea and vomiting associated with exenatide treatment: a retrospective analysis of an open-label, parallel-group, single-dose study in healthy subjects.
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Prophylactic use of anti-emetic medications reduced nausea and vomiting associated with exenatide treatment: a retrospective analysis of an open-label, parallel-group, single-dose study in healthy subjects.

机译:预防性使用止吐药可减少与艾塞那肽治疗相关的恶心和呕吐:一项针对健康受试者的开放标签,平行分组,单剂量研究的回顾性分析。

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AIMS: Transient nausea and, to a lesser extent, vomiting are common adverse effects of exenatide that can be mitigated by dose titration and usually do not result in treatment discontinuation. This retrospective analysis of data from a phase 1, open-label, parallel-group, single-dose study in healthy subjects evaluated the effect of oral anti-emetics on exenatide-associated nausea and vomiting and on the pharmacokinetics of exenatide. METHODS: A single subcutaneous dose (10 mug) of exenatide was administered to 120 healthy subjects (19-65 years, BMI 23-35 kg/m(2) ). Incidences of nausea and vomiting were compared between 60 subjects premedicated with two oral anti-emetics 30 min before the exenatide dose and 60 non-premedicated subjects. Similarly, the area under the concentration-time curve (AUC) and the maximum observed concentration (C(max) ) of plasma exenatide concentrations over 8 h post-dose were compared. RESULTS: Among all subjects [61% male, 32 +/- 12 years, body mass index (BMI) 29.1 +/- 3.4 kg/m(2) (mean +/- sd)], mild to moderate nausea was the most frequent adverse event after exenatide dosing. Vomiting was also observed. Subjects premedicated with anti-emetics experienced significantly less nausea and vomiting (16.7 and 6.7%, respectively) vs. non-premedicated subjects (61.7 and 38.3%, respectively; P-value <0.0001 for both nausea and vomiting). The mean area under the concentration-time curve and the maximum observed concentration AUC and C(max) of plasma exenatide concentrations during 8 h post-dose were not significantly different between groups. CONCLUSION: Administration of oral anti-emetics before a single 10-mug exenatide dose was associated with significant reductions in treatment-emergent nausea and vomiting, with no discernible effect on the pharmacokinetics of exenatide. Use of anti-emetic therapy may provide a short-term strategy to minimize the nausea and vomiting associated with exenatide treatment.
机译:目的:短暂性恶心和呕吐是艾塞那肽的常见不良反应,可通过剂量滴定缓解,通常不会导致治疗中断。这项对健康受试者的1期,开放标签,平行组,单剂量研究的数据进行的回顾性分析评估了口服止吐药对艾塞那肽相关的恶心和呕吐以及艾塞那肽药代动力学的影响。方法:对120名健康受试者(19-65岁,BMI 23-35 kg / m(2))给予单次皮下剂量(10杯)艾塞那肽。比较了在艾塞那肽用药30分钟前用两种口服止吐药进行预治疗的60名受试者和60名未进行预治疗的受试者之间的恶心和呕吐发生率。类似地,比较了剂量-时间曲线下的面积(AUC)和用药后8小时内血浆艾塞那肽浓度的最大观测浓度(C(max))。结果:在所有受试者中[61%男性,32 +/- 12岁,体重指数(BMI)29.1 +/- 3.4 kg / m(2)(平均+/- sd)],轻度至中度恶心是最艾塞那肽给药后频繁发生不良事件。还观察到呕吐。与未接受过药物治疗的受试者(分别为61.7%和38.3%;恶心和呕吐的P值<0.0001)相比,接受止吐药治疗的受试者的恶心和呕吐显着减少(分别为16.7和6.7%)。给药后8小时内,浓度-时间曲线下的平均面积和血浆艾塞那肽浓度的最大观测浓度AUC和C(max)无显着差异。结论:在单剂10杯艾塞那肽剂量之前给予口服止吐药可显着减少紧急治疗中的恶心和呕吐,对艾塞那肽的药代动力学没有明显影响。使用止吐药可能会提供一种短期策略,以最大程度减少与艾塞那肽治疗相关的恶心和呕吐。

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