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A comparative pharmacokinetic and tolerability analysis of the novel orotic acid salt form of tenofovir disoproxil and the fumaric acid salt form in healthy subjects

机译:替诺福韦二磺酸新乳清酸盐形式和富马酸盐形式在健康受试者中的比较药代动力学和耐受性分析

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摘要

A novel orotic acid salt form of tenofovir disoproxil (DA-2802) was developed and is expected to replace the fumaric acid salt form. The pharmacokinetic (PK) characteristics and tolerability profiles of DA-2802 were compared to those of tenofovir disoproxil fumarate (TDF, Viread®) in healthy subjects. A randomized, open-label, single-dose study was conducted in 36 healthy subjects using a two-treatment, two-period, and two-sequence crossover design. Subjects received a single oral dose of 319 mg DA-2802 or 300 mg TDF, during each period, with a 7-day washout. Serial blood samples were collected pre-dosing and up to 72 hours post-dosing in each period, for determination of serum tenofovir concentration, which was measured by ultra-performance liquid chromatography-tandem mass spectrometry. A non-compartmental method was used to obtain PK parameters of tenofovir. For comparison between the two tenofovir disoproxil salts, the 90% confidence intervals (90% CIs) of geometric mean ratios of DA-2802 to TDF for the maximum concentration (Cmax) and the area under the concentration–time curve to the last quantifiable concentration (AUC0–t) were determined. The tolerability profiles of tenofovir were assessed by evaluation of adverse events and vital signs, physical examination, ECG, and clinical laboratory tests. The serum tenofovir concentration–time profiles of DA-2802 or TDF were comparable in 32 subjects who completed the study. In both profiles, a two-compartmental elimination with first-order elimination kinetics in the terminal phase was reported in a few subjects, showing a secondary peak in the initial phase of elimination. The geometric mean ratio (90% CI) of DA-2802 to TDF was 0.898 (0.815–0.990) for Cmax and 0.904 (0.836–0.978) for AUC0–t. There were no clinically significant findings in the tolerability assessments. DA-2802 showed comparable PK characteristics and tolerability profiles to TDF.
机译:开发了一种新的替诺福韦二甲氧萘磺酸乳清酸盐形式(DA-2802),并有望替代富马酸盐形式。比较了DA-2802与替诺福韦富马酸替诺福韦酯(TDF,Viread ®)的药代动力学(PK)特征和耐受性特征。一项随机,开放标签,单剂量的研究在36位健康受试者中进行了两次治疗,两个时期和两个序列的交叉设计。在每个期间,受试者接受单次口服剂量319 mg DA-2802或300 mg TDF,洗脱期为7天。在给药前和给药后最多72小时内收集系列血样,以测定血清替诺福韦浓度,用超高效液相色谱-串联质谱法测定。使用非房室方法获得替诺福韦的PK参数。为了比较两种替诺福韦二钠盐,最大浓度(Cmax)的DA-2802与TDF几何平均比的90%置信区间(90%CI),以及浓度-时间曲线下的面积至最后可量化浓度(AUC0–t)被确定。通过评估不良事件和生命体征,体格检查,心电图和临床实验室测试评估替诺福韦的耐受性。在完成这项研究的32位受试者中,DA-2802或TDF的血清替诺福韦浓度-时间曲线可比。在两个配置文件中,在一些受试者中均报告了在末期具有二阶消除动力学的二室消除,显示了消除初始阶段的次要峰。对于Cmax,DA-2802与TDF的几何平均比率(90%CI)为0.898(0.815–0.990),对于AUC0–t为0.904(0.836–0.978)。在耐受性评估中没有临床上重要的发现。 DA-2802具有与TDF相当的PK特性和耐受性。

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