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.

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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