DaVita Clinical Research, Minneapolis, Minnesota, USA.
Paratek Pharmaceuticals Inc., King of Prussia, Pennsylvania, USA.
Antimicrob Agents Chemother. 2018 Jan 25;62(2). doi: 10.1128/AAC.02057-17. Print 2018 Feb.
Many antibiotics require dose adjustments in patients with renal impairment and/or in those undergoing hemodialysis. Omadacycline, the first aminomethylcycline antibiotic in late-stage clinical development, displays activity against a broad spectrum of bacterial pathogens, including drug-resistant strains. Data from completed phase 3 studies of omadacycline for the treatment of acute bacterial skin and skin structure infections (ABSSSI) and community-acquired bacterial pneumonia (CABP) showed intravenous (i.v.) to once-daily oral omadacycline to be clinically effective and well tolerated. To determine if the dosing of omadacycline should be adjusted in patients with impaired renal function, a phase 1 study examining the pharmacokinetics (PK) and safety of i.v. omadacycline (100 mg) was conducted in subjects with end-stage renal disease (ESRD) on stable hemodialysis ( = 8) and in matched healthy subjects ( = 8). i.v. administration of omadacycline produced similar plasma concentration-time profiles in subjects with ESRD and healthy subjects. Further, in subjects with ESRD, similar values of the PK parameters were observed when omadacycline was administered i.v. after or before dialysis. The mean area under the concentration-time curve from time zero extrapolated to infinity in plasma was 10.30 μg · h/ml when omadacycline was administered to ESRD subjects after dialysis, 10.20 μg · h/ml when omadacycline was administered to ESRD subjects before dialysis, and 9.76 μg · h/ml when omadacycline was administered to healthy subjects. The mean maximum observed concentration of omadacycline in plasma in ESRD subjects was 1.88 μg/ml when it was administered after dialysis and 2.33 μg/ml when it was administered before dialysis, and in healthy subjects it was 1.92 μg/ml. The 100-mg i.v. dose of omadacycline was generally safe and well tolerated in both ESRD and healthy subjects. This study demonstrates that no dose adjustment is necessary for omadacycline in patients with impaired renal function or on days when patients are receiving hemodialysis.
许多抗生素在肾功能受损的患者和/或接受血液透析的患者中需要调整剂量。奥马环素是临床开发后期的第一个氨甲基环素抗生素,对广泛的细菌病原体具有活性,包括耐药菌株。奥马环素治疗急性细菌性皮肤和皮肤结构感染(ABSSSI)和社区获得性细菌性肺炎(CABP)的完成的 3 期研究数据表明,静脉(i.v.)至每日一次口服奥马环素具有临床疗效且耐受性良好。为了确定肾功能受损患者是否需要调整奥马环素的剂量,一项研究奥马环素(100mg)的药代动力学(PK)和安全性的 1 期研究在稳定血液透析的终末期肾病(ESRD)患者(n=8)和匹配的健康受试者(n=8)中进行。在 ESRD 患者和健康受试者中,静脉注射奥马环素产生了相似的血浆浓度-时间曲线。此外,在 ESRD 患者中,当奥马环素在透析后或透析前静脉给药时,观察到相似的 PK 参数值。奥马环素在 ESRD 患者中透析后给药时,从时间零外推至无穷大的血浆 AUC0-∞为 10.30μg·h/ml,透析前给药时为 10.20μg·h/ml,健康受试者时为 9.76μg·h/ml。在 ESRD 患者中,奥马环素的平均最大观测血浆浓度为透析后给药时为 1.88μg/ml,透析前给药时为 2.33μg/ml,健康受试者时为 1.92μg/ml。奥马环素 100mg 的静脉剂量在 ESRD 患者和健康受试者中通常是安全且耐受良好的。这项研究表明,在肾功能受损的患者或接受血液透析的日子里,奥马环素不需要调整剂量。