Zhang Chuhan, Yu Shuyan, Li Size, Wu Xiaojie, Wei Qiong, He Jinjie, Cao Guoying, Yang Haijing, Wang Jingjing, Fujitani Kohei, Katsube Takayuki, Zhang Jing, Dou Honghong
Phase I Clinical Trial Center, Huashan Hospital, Fudan University, Shanghai, China.
Institute of Antibiotics, Huashan Hospital, Fudan University, Shanghai, China.
Adv Ther. 2025 May;42(5):2285-2297. doi: 10.1007/s12325-025-03147-1. Epub 2025 Mar 13.
We aim to evaluate the safety and pharmacokinetic (PK) properties of cefiderocol in Chinese participants, following single and subsequent multiple administrations of 2 g q8h with 3-h intravenous infusion, and to predict its efficacy for the treatment of Gram-negative bacilli (GNB) infection based on PK/pharmacodynamic (PD) analysis.
This was an open-label, single-center, single- and multiple-dose phase I study, conducted from September 2022 to October 2022, with 12 eligible healthy Chinese adults (6 men and 6 women). The PK profiles were described by noncompartmental analysis and a two-compartment model using WinNonlin (v.8.1). Monte Carlo simulations (MCS) were performed by R (v.4.3.1) to obtain the probability of target attainment (PTA) as well as the cumulative fraction of response (CFR), based on the previously published data of susceptibility studies for cefiderocol in China.
Both single and multiple doses of 2 g cefiderocol were well tolerated in healthy Chinese subjects, and no severe treatment-emergent adverse events occurred. The maximum plasma concentration of cefiderocol was observed approximately 3 h after administration and the half-life was about 2.6 h, with no accumulation after multiple dosing. It is worth noting that, the PK profiles, including CL, V1, C, C, and AUC, were consistent with those of other populations, e.g., Caucasian. PK/PD analysis and MCS suggested that standard dosage regimen of cefiderocol would achieve satisfactory PTA and CFR (exceeding 90%) for Gram-negative pathogens with MICs up to 4 μg/mL, using the proposed fT target of 75.0%. Consistently, more than 90% of PTA was reached for Enterobacterales, P. aeruginosa, and Acinetobacter spp. with MICs up to 4 μg/mL at their respective 73.3%, 72.2%, and 88.1% fT targets, with CFR exceeding 95%. Especially for S. maltophilia, both the PTA and CFR reached nearly 100% for those with MICs as high as 8 μg/mL.
Cefiderocol is well tolerated by Chinese healthy participants at the dosage regimen of 2 g cefiderocol q8h via 3-h infusion, which is expected to achieve satisfactory efficacy in treating GNB infections in China, although further data for model optimization might still be required. To our knowledge, this is the first study to describe the PK properties of cefiderocol in Chinese subjects, and to predict its microbiological efficacy for treating GNB infection in China.
ChiCTR2300076607.
我们旨在评估在中国受试者中单次及随后多次给予2克、每8小时一次、静脉输注3小时的头孢地尔的安全性和药代动力学(PK)特性,并基于PK/药效学(PD)分析预测其治疗革兰氏阴性杆菌(GNB)感染的疗效。
这是一项开放标签、单中心、单剂量和多剂量的I期研究,于2022年9月至2022年10月进行,纳入了12名符合条件的中国健康成年人(6名男性和6名女性)。使用WinNonlin(v.8.1)通过非房室分析和二室模型描述PK曲线。基于之前在中国发表的头孢地尔敏感性研究数据,使用R(v.4.3.1)进行蒙特卡洛模拟(MCS),以获得目标达成概率(PTA)以及反应累积分数(CFR)。
单次和多次给予2克头孢地尔在中国健康受试者中耐受性良好,未发生严重的治疗中出现的不良事件。头孢地尔的最大血浆浓度在给药后约3小时观察到,半衰期约为2.6小时,多次给药后无蓄积。值得注意的是,包括清除率(CL)、中央室分布容积(V1)、峰浓度(Cmax)、谷浓度(Cmin)和药时曲线下面积(AUC)在内的PK曲线与其他人群(如白种人)一致。PK/PD分析和MCS表明,对于最低抑菌浓度(MIC)高达4μg/mL的革兰氏阴性病原体,使用提议的75.0%的游离药物浓度时间(fT)目标,头孢地尔的标准给药方案将实现令人满意的PTA和CFR(超过90%)。同样,对于肠杆菌科、铜绿假单胞菌和不动杆菌属,当MIC高达4μg/mL时,在各自73.3%、72.2%和88.1%的fT目标下,PTA超过90%,CFR超过95%。特别是对于嗜麦芽窄食单胞菌,对于MIC高达8μg/mL的菌株,PTA和CFR均接近100%。
在中国健康受试者中,通过3小时输注每8小时给予一次2克头孢地尔的给药方案耐受性良好,尽管可能仍需要进一步的数据来优化模型,但预计该方案在中国治疗GNB感染时将取得令人满意的疗效。据我们所知,这是第一项描述头孢地尔在中国受试者中的PK特性,并预测其在中国治疗GNB感染的微生物学疗效的数据。
ChiCTR2300076607