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Pharmacokinetics and Safety of Omadacycline in Subjects with Impaired Renal Function
Jolene K Berg1, Evan Tzanis2, Lynne Garrity-Ryan3
1DaVita Clinical Research, Minneapolis, Minnesota, USA.
Abstract:
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 (n = 8) and in matched healthy subjects (n = 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.
Insights
Omadacycline, an aminomethylcycline antibiotic, does not require dose adjustments in patients with end-stage renal disease (ESRD) or those on hemodialysis. Pharmacokinetic studies showed similar safety and tolerability profiles, confirming no dose modification is needed for renal impairment.
Area of Science:
- Pharmacology and Nephrology
- Antimicrobial Pharmacokinetics
- Drug Development and Clinical Trials
Background:
- Many antibiotics necessitate dose adjustments for patients with renal impairment or undergoing hemodialysis.
- Omadacycline is a novel aminomethylcycline antibiotic with broad-spectrum activity, including against resistant pathogens.
- Previous Phase 3 studies confirmed the clinical efficacy and tolerability of omadacycline for ABSSSI and CABP.
Purpose of the Study:
- To evaluate the pharmacokinetics (PK) and safety of intravenous (i.v.) omadacycline in patients with end-stage renal disease (ESRD).
- To determine if omadacycline dosing requires adjustment in individuals with impaired renal function or on hemodialysis.
- To compare PK parameters and safety of omadacycline between ESRD subjects and healthy controls.
Main Methods:
- A Phase 1 pharmacokinetic study administered a 100 mg i.v. dose of omadacycline.
- Participants included 8 subjects with ESRD on stable hemodialysis and 8 matched healthy subjects.
- PK profiles and safety were assessed in ESRD subjects before and after hemodialysis, and in healthy subjects.
Main Results:
- Intravenous omadacycline exhibited similar plasma concentration-time profiles in ESRD subjects and healthy controls.
- PK parameters, including area under the curve (AUC) and maximum concentration (Cmax), were comparable across groups.
- The 100 mg i.v. dose of omadacycline was generally safe and well-tolerated in both ESRD and healthy populations.
Conclusions:
- Omadacycline pharmacokinetics are not significantly altered by end-stage renal disease or hemodialysis.
- No dose adjustment for omadacycline is necessary in patients with impaired renal function or those undergoing hemodialysis.
- Omadacycline demonstrates a favorable safety and tolerability profile in renally impaired populations.
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