Wu Xiao-jie, Zhang Jing, Guo Bei-ning, Zhang Ying-yuan, Yu Ji-cheng, Cao Guo-ying, Chen Yuan-cheng, Zhu De-mei, Ye Xin-yu, Wu Ju-fang, Shi Yao-guo, Chang Li-wen, Chang Yu-ting, Tsai Cheng-yuan
Institute of Antibiotics, Huashan Hospital, Fudan University, Shanghai, China Key Laboratory of Clinical Pharmacology of Antibiotics, Ministry of Health, Shanghai, China.
Institute of Antibiotics, Huashan Hospital, Fudan University, Shanghai, China Key Laboratory of Clinical Pharmacology of Antibiotics, Ministry of Health, Shanghai, China
Antimicrob Agents Chemother. 2015 Mar;59(3):1446-54. doi: 10.1128/AAC.04039-14. Epub 2014 Dec 22.
This study evaluated the safety and pharmacokinetic/pharmacodynamic profiles of nemonoxacin in healthy Chinese volunteers following multiple-dose intravenous infusion once daily for 10 consecutive days. The study was composed of two stages. In the open-label stage, 500 mg or 750 mg of nemonoxacin (n = 12 each) was administered at an infusion rate of 5.56 mg/min. In the second stage, with a randomized double-blind placebo-controlled design, 500, 650, or 750 mg of nemonoxacin (n = 16 in each cohort; 12 subjects received the drug and the other 4 subjects received the placebo) was given at an infusion rate of 4.17 mg/min. The results showed that, in the first stage, the maximal nemonoxacin concentrations (mean ± SD) at steady state (Cmax_ss) were 9.60 ± 1.84 and 11.04 ± 2.18 μg/ml in the 500-mg and 750-mg cohorts, respectively; the areas under the concentration-time curve at steady state (AUC0-24_ss) were 44.03 ± 8.62 and 65.82 ± 10.78 μg · h/ml in the 500-mg and 750-mg cohorts, respectively. In the second stage, the nemonoxacin Cmax_ss values were 7.13 ± 1.47, 8.17 ± 1.76, and 9.96 ± 2.23 μg/ml in the 500-mg, 650-mg, and 750-mg cohorts, respectively; the AUC0-24_ss values were 40.46 ± 9.52, 54.17 ± 12.10, and 71.34 ± 17.79 μg · h/ml in the 500-mg, 650-mg, and 750-mg cohorts, respectively. No accumulation was found after the 10-day infusion with any regimen. The drug was well tolerated. A Monte Carlo simulation indicated that the cumulative fraction of response of any dosing regimen was nearly 100% against Streptococcus pneumoniae. The probability of target attainment of nemonoxacin therapy was >98% when the MIC of nemonoxacin against S. pneumoniae was ≤1 mg/liter. It is suggested that all of the studied intravenous nemonoxacin dosing regimens should have favorable clinical and microbiological efficacies in future clinical studies. (This study has been registered at ClinicalTrials.gov under registration no. NCT01944774.).
本研究评估了健康中国志愿者连续10天每日一次多次静脉输注奈诺沙星后的安全性及药代动力学/药效学特征。该研究分为两个阶段。在开放标签阶段,以5.56 mg/min的输注速率给予500 mg或750 mg奈诺沙星(每组n = 12)。在第二阶段,采用随机双盲安慰剂对照设计,以4.17 mg/min的输注速率给予500、650或750 mg奈诺沙星(每个队列n = 16;12名受试者接受药物,另外4名受试者接受安慰剂)。结果显示,在第一阶段,500 mg和750 mg队列中稳态时奈诺沙星的最大浓度(均值±标准差)(Cmax_ss)分别为9.60±1.84和11.04±2.18 μg/ml;500 mg和750 mg队列中稳态时浓度-时间曲线下面积(AUC0-24_ss)分别为44.03±8.62和65.82±10.78 μg·h/ml。在第二阶段,500 mg、650 mg和750 mg队列中奈诺沙星的Cmax_ss值分别为7.13±1.47、8.17±1.76和9.96±2.23 μg/ml;500 mg、650 mg和750 mg队列中AUC0-24_ss值分别为40.46±9.52、54.17±12.10和71.34±17.79 μg·h/ml。10天输注任何方案后均未发现蓄积。该药物耐受性良好。蒙特卡洛模拟表明,任何给药方案对肺炎链球菌的累积反应分数接近100%。当奈诺沙星对肺炎链球菌的最低抑菌浓度(MIC)≤1 mg/L时,奈诺沙星治疗达到目标的概率>98%。提示所有研究的静脉输注奈诺沙星给药方案在未来临床研究中应具有良好的临床和微生物学疗效。(本研究已在ClinicalTrials.gov注册,注册号为NCT01944774。)