Amylin Pharmaceuticals Inc., San Diego, CA 92121, USA.
Diabet Med. 2010 Oct;27(10):1168-73. doi: 10.1111/j.1464-5491.2010.03085.x.
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.
A single subcutaneous dose (10 μg) 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.
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.
Administration of oral anti-emetics before a single 10-μg 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.
外泌体诱导的短暂性恶心,在一定程度上还有呕吐,是外泌体的常见不良反应,可以通过剂量滴定来缓解,通常不会导致治疗中断。这项对健康受试者进行的 1 期、开放标签、平行组、单次剂量研究数据的回顾性分析评估了口服止吐药对外泌体相关恶心和呕吐的影响,以及对外泌体药代动力学的影响。
120 名健康受试者(19-65 岁,BMI 23-35kg/m2)接受单次皮下剂量(10μg)外泌体。比较 60 名预先使用两种口服止吐药 30 分钟后接受外泌体剂量的受试者和 60 名未预先使用止吐药的受试者的恶心和呕吐发生率。同样,比较 8 小时内的血浆外泌体浓度的曲线下面积(AUC)和最大观察浓度(C(max))。
在所有受试者中(61%为男性,32±12 岁,体重指数(BMI)29.1±3.4kg/m2(平均值±标准差)),外泌体给药后最常见的不良事件是轻度至中度恶心。也观察到呕吐。与未预先使用止吐药的受试者(61.7%和 38.3%)相比,预先使用止吐药的受试者恶心和呕吐的发生率明显较低(分别为 16.7%和 6.7%;恶心和呕吐的 P 值均<0.0001)。8 小时内的血浆外泌体浓度的平均 AUC 和 C(max)在两组之间无显著差异。
在单次 10μg 外泌体剂量前给予口服止吐药与治疗中出现的恶心和呕吐显著减少相关,对外泌体药代动力学无明显影响。止吐治疗的短期策略可能有助于最大限度地减少外泌体治疗相关的恶心和呕吐。