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单剂量安全性、耐受性和药代动力学的抗生素 GSK1322322,一种新型的肽脱甲酰酶抑制剂。

Single-dose safety, tolerability, and pharmacokinetics of the antibiotic GSK1322322, a novel peptide deformylase inhibitor.

机构信息

GlaxoSmithKline, Research Triangle Park, North Carolina, USA.

出版信息

Antimicrob Agents Chemother. 2013 May;57(5):2005-9. doi: 10.1128/AAC.01779-12. Epub 2013 Feb 12.

Abstract

GSK1322322 is a potent inhibitor of peptide deformylase, an essential bacterial enzyme required for protein maturation. GSK1322322 is active against community-acquired skin and respiratory tract pathogens, including methicillin-resistant Staphylococcus aureus, multidrug-resistant Streptococcus pneumoniae, and atypical pathogens. This phase I, randomized, double-blind, placebo-controlled, 2-part, single-dose, dose escalation study (first time in humans) evaluated the safety, tolerability, and pharmacokinetics of GSK1322322 (powder-in-bottle formulation) in healthy volunteers. In part A, dose escalation included GSK1322322 doses of 100, 200, 400, 800, and 1,500 mg under fasting conditions and 800 mg administered with a high-fat meal. In part B, higher doses of GSK1322322 (2,000, 3,000, and 4,000 mg) were evaluated under fasting conditions. Of the 39 volunteers enrolled in the study, 29 and 10 volunteers were treated with GSK1322322 and placebo, respectively. Upon single-dose administration, GSK1322322 was absorbed rapidly, with median times to maximum plasma concentration (T(max)) ranging from 0.5 to 1.0 h. The maximum observed plasma concentration (C(max)) and exposure (area under the concentration-time curve [AUC]) of GSK1322322 were greater than dose proportional between 100 and 1,500 mg and less than dose proportional between 1,500 and 4,000 mg. Administration of the drug with a high-fat meal reduced the rate of absorption (reduced C(max) and delayed T(max)) without affecting the extent of absorption (no effect on AUC). GSK1322322 was generally well tolerated, with all adverse events being mild to moderate in intensity during both parts of the study. The most frequently reported adverse event was headache. Data from this study support further evaluation of GSK1322322.

摘要

GSK1322322 是一种有效的肽脱甲酰酶抑制剂,这是一种细菌成熟所必需的酶。GSK1322322 对社区获得性皮肤和呼吸道病原体具有活性,包括耐甲氧西林金黄色葡萄球菌、多药耐药性肺炎链球菌和非典型病原体。这项 I 期、随机、双盲、安慰剂对照、两部分、单次剂量、剂量递增研究(首次在人体中进行)评估了 GSK1322322(瓶装粉末制剂)在健康志愿者中的安全性、耐受性和药代动力学。在 A 部分,剂量递增包括禁食条件下 GSK1322322 剂量为 100、200、400、800 和 1,500mg,以及高脂肪餐时给予 800mg。在 B 部分,评估了禁食条件下 GSK1322322 的更高剂量(2,000、3,000 和 4,000mg)。在这项研究中,有 39 名志愿者被纳入研究,其中 29 名志愿者接受了 GSK1322322 治疗,10 名志愿者接受了安慰剂治疗。单次给药后,GSK1322322 迅速被吸收,最大血浆浓度(T(max))中位数在 0.5 至 1.0 小时之间。GSK1322322 的最大观察到的血浆浓度(C(max))和暴露量(浓度-时间曲线下面积[AUC])在 100 至 1500mg 之间大于剂量比例,在 1500 至 4000mg 之间小于剂量比例。高脂肪餐给药可降低吸收速度(降低 C(max)并延迟 T(max)),而不影响吸收程度(对 AUC 无影响)。GSK1322322 一般耐受性良好,在研究的两部分中,所有不良事件的严重程度均为轻度至中度。报告最频繁的不良事件是头痛。这项研究的数据支持进一步评估 GSK1322322。

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