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在健康成年人空腹条件下,单次给药、3 种交叉药代动力学比较:具有厌恶技术的盐酸羟考酮速释制剂(IRO-A,Oxecta)、IRO-a 与烟酸、盐酸羟考酮(Roxicodone)。

A single-dose, 3-way crossover pharmacokinetic comparison between immediate-release oxycodone hydrochloride with aversion technology (IRO-A, Oxecta), IRO-a with Niacin, and Oxycodone Hydrochloride (Roxicodone) in healthy adults under fasting conditions.

机构信息

1Clinical Research Services, Worldwide Clinical Trials Drug Development Solutions, San Antonio, TX; and 2Technical Affairs, Acura Pharmaceuticals Inc, Palatine, IL.

出版信息

Am J Ther. 2014 Mar-Apr;21(2):99-105. doi: 10.1097/MJT.0b013e3182456d9b.

Abstract

Snorting and intravenous use are common routes of administration for advanced opioid abusers. A tablet form of immediate-release oxycodone (IRO) developed using Aversion Technology combines immediate release (IR) oxycodone HCl with inactive functional excipients that are intended to discourage tampering associated with intranasal and intravenous abuse (IRO-A; Oxecta, Pfizer). The purpose of this single-dose, open-label, randomized, 3-period, 3-treatment crossover study was to evaluate the bioequivalence of IRO-A to the marketed immediate-release oxycodone HCl (IRO; Roxicodone, Xanodyne Pharmaceuticals Inc., Newport, KY). IRO-A was also compared with IRO-A with niacin, a product previously developed containing the same functional excipients plus niacin as an aversive agent to discourage oral overconsumption. Healthy adults (N = 40) aged 18-55 years received single 15-mg doses of IRO-A, IRO-A with niacin (60 mg), or IRO after fasting overnight. Naltrexone was administered to diminish opioid effects. Doses were separated by a ≥7-day washout. Plasma samples taken at designated time points were analyzed using liquid chromatography with tandem mass spectrometry. Geometric mean ratios for ln-transformed parameters for IRO-A and IRO were 92%, 104%, and 104% for Cmax, AUClast (AUC is area under the concentration-time curve), and AUCinf; 90% confidence intervals were within the accepted 80%-125% range. IRO-A was also bioequivalent to IRO-A with niacin. Adverse events were mild to moderate in intensity and typical of opioid therapy (nausea, headache, vomiting). Flushing only occurred when the subjects received the IRO-A with niacin treatment (9/37 subjects). The results demonstrated that IRO-A is bioequivalent to IRO and IRO-A with niacin. With features designed to discourage tampering associated with common forms of abuse, IRO-A may provide an alternative to conventional immediate-release oxycodone formulations.

摘要

嗅吸和静脉注射是晚期阿片类药物滥用者常见的给药途径。一种使用厌恶技术开发的即时释放羟考酮(IRO)片剂,将即时释放(IR)羟考酮盐酸盐与惰性功能赋形剂结合在一起,旨在阻止与鼻内和静脉内滥用相关的篡改(IRO-A;Oxecta,辉瑞)。这项单剂量、开放标签、随机、3 期、3 种治疗交叉研究的目的是评估 IRO-A 与市售即时释放羟考酮盐酸盐(IRO;Roxicodone,Xanodyne Pharmaceuticals Inc.,Newport,KY)的生物等效性。还比较了 IRO-A 与烟酸的制剂,该产品以前开发的含有相同的功能赋形剂和烟酸作为厌恶剂,以阻止口服过度消耗。年龄在 18-55 岁的健康成年人(N=40)空腹过夜后接受单剂量 15mg 的 IRO-A、IRO-A 与烟酸(60mg)或 IRO。给予纳曲酮以减少阿片类药物的作用。剂量间隔至少 7 天清洗期。使用液相色谱-串联质谱法分析指定时间点采集的血浆样本。IRO-A 和 IRO 的 ln 转换参数的几何均数比值分别为 Cmax、AUClast(AUC 为浓度-时间曲线下面积)和 AUCinf 的 92%、104%和 104%;90%置信区间在可接受的 80%-125%范围内。IRO-A 也与 IRO-A 与烟酸具有生物等效性。不良反应的强度为轻度至中度,与阿片类药物治疗典型(恶心、头痛、呕吐)。只有当受试者接受 IRO-A 与烟酸治疗时才会出现潮红(37 名受试者中的 9 名)。结果表明,IRO-A 与 IRO 和 IRO-A 与烟酸具有生物等效性。IRO-A 具有阻止与常见滥用形式相关的篡改的特征,可能为传统即时释放羟考酮制剂提供替代方案。

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