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在肾功能受损和需要血液透析的受试者中单次静脉注射左氟沙星后的药代动力学和安全性。

Pharmacokinetics and safety of lefamulin after single intravenous dose administration in subjects with impaired renal function and those requiring hemodialysis.

机构信息

Nabriva Therapeutics GmbH, Vienna, Austria.

Orlando Clinical Research Center, Orlando, Florida, USA.

出版信息

Pharmacotherapy. 2021 May;41(5):451-456. doi: 10.1002/phar.2523.

Abstract

STUDY OBJECTIVE

Lefamulin is a novel IV and oral pleuromutilin recently approved for the treatment of community-acquired bacterial pneumonia (CABP). Given that renal comorbidities are common in patients admitted for CABP, understanding the pharmacokinetics of lefamulin in the face of severe renal impairment, including those requiring hemodialysis, is needed.

DESIGN

Open-label, Phase-1 pharmacokinetic study.

SETTING

Research Study Center.

PATIENTS

Twenty-three matched subjects were included, seven with "Normal" renal function (creatinine clearance >90 ml/min), eight with "Severe" renal impairment (glomerular filtration rate <30 ml/min/1.73 m ), and eight subjects requiring hemodialysis.

MEASUREMENTS AND MAIN RESULTS

Subjects were administered a single dose of lefamulin IV 150 mg as a 1-h infusion. Subjects in the hemodialysis group started hemodialysis within 1 h after lefamulin infusion (On dialysis), as well as, on a non-dialysis day (Off dialysis). Plasma, urine, and dialysate fluid were collected for 36 h and analyzed for lefamulin and its major metabolite, BC-8041. Lefamulin was primarily excreted non-renally across groups. Statistical analyses revealed lefamulin and BC-8041 pharmacokinetics were similar between Normal and Severe groups, except for renal clearance, which decreased in Severe subjects (mean 1.3 L/h Normal vs. 0.4 L/h Severe). Likewise, lefamulin pharmacokinetics during on and off dialysis were unchanged, with lefamulin not measurably filtered in dialysate fluid. Two, three, and three subjects reported drug-related treatment-emergent adverse events (TEAE) in Normal, Severe, and Hemodialysis groups, respectively. All TEAEs were mild, except one (infusion-site reaction) that was classified as moderate.

CONCLUSION

No dosage adjustment is required for patients with renal impairment, and lefamulin can be administered without regard to hemodialysis timing.

摘要

研究目的

lefamulin 是一种新型 IV 和口服截短侧耳素,最近被批准用于治疗社区获得性细菌性肺炎(CABP)。鉴于 CABP 住院患者常合并肾脏合并症,因此需要了解 lefamulin 在严重肾功能损害(包括需要血液透析的患者)情况下的药代动力学。

设计

开放标签、I 期药代动力学研究。

设置

研究中心。

患者

共纳入 23 例匹配患者,7 例肾功能“正常”(肌酐清除率>90ml/min),8 例肾功能“严重”损害(肾小球滤过率<30ml/min/1.73m),8 例需要血液透析的患者。

测量和主要结果

受试者单次静脉给予 lefamulin 150mg,1 小时输注。血液透析组患者在 lefamulin 输注后 1 小时内开始血液透析(透析时),以及非透析日(透析时)。采集 36 小时的血浆、尿液和透析液进行 lefamulin 及其主要代谢物 BC-8041 的分析。lefamulin 在各研究组主要经非肾脏途径排泄。统计分析显示,除肾脏清除率外,lefamulin 和 BC-8041 的药代动力学在正常和严重组之间相似,正常组的肾脏清除率(mean 1.3 L/h Normal vs. 0.4 L/h Severe)降低。同样,在透析和非透析期间 lefamulin 的药代动力学无变化,lefamulin 不能在透析液中被检测到。正常、严重和血液透析组分别有 2、3 和 3 例患者报告了与药物相关的治疗后出现的不良事件(TEAE)。所有 TEAEs 均为轻度,除 1 例(输注部位反应)为中度外。

结论

肾功能损害患者无需调整剂量,lefamulin 可无需考虑血液透析时间进行给药。

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