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Effect of a high-calorie, high-fat meal on the bioavailability and pharmacokinetics of PA-824 in healthy adult subjects

机译:高热量,高脂肪餐对健康成人受试者PA-824的生物利用度和药代动力学的影响

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摘要

PA-824 is a novel nitroimidazo-oxazine being developed as an antituberculosis agent. Two randomized studies evaluated the pharmacokinetics and safety of a single oral dose of PA-824 administered to healthy adult subjects 30 min after a high-calorie, high-fat meal (fed state) versus after a minimum 10-h fast (fasted state). A total of 48 subjects were dosed in the two studies in a randomized crossover design with PA-824 at dose levels of 50, 200, or 1,000 mg in the fed state or fasted state. After the administration of PA-824, the geometric mean ratios of Cmax and AUC0-∞ revealed an increase in exposure with the addition of a highcalorie, high-fat meal compared to the fasted state by 140 and 145% at 50 mg, 176 and 188% at 200 mg, and 450 and 473% at 50, 200, and 1,000 mg, respectively. The median Tmax in the fed state was 4 h for the 50-mg dose and 5 h for the 200- and 1,000-mg doses. In the fasted state, the median Tmax was 4 h for the 50- and 200-mg doses and 6.5 h for the 1,000-mg dose. All doses were well tolerated, and no serious adverse events occurred in either study.
机译:PA-824是一种新型的硝基咪唑并恶嗪,已被开发为抗结核药。两项随机研究评估了高热量,高脂肪餐(进食状态)后至少30小时禁食(禁食状态)后30分钟向健康成人受试者单次口服PA-824的药代动力学和安全性。在两项研究中,共有48位受试者以随机交叉设计的PA-824剂量在进食状态或禁食状态下分别为50、200或1,000 mg。服用PA-824后,Cmax和AUC0-∞的几何平均比显示,与空腹状态相比,添加高热量,高脂肪的膳食后,暴露量增加,在50 mg,176和50 mg下禁食状态分别增加140和145%。 200 mg分别为188%,50、200和1,000 mg分别为450和473%。在50毫克剂量的进食状态下,中值Tmax为4小时,而在200毫克和1,000毫克剂量下为5小时。在禁食状态下,50和200 mg剂量的中值Tmax为4 h,而1,000 mg剂量的中值Tmax为6.5 h。所有剂量均耐受良好,在两项研究中均未发生严重不良事件。

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