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Clinical Trial
. 2006 Oct;50(10):3245-9.
doi: 10.1128/AAC.00247-06.

Pharmacokinetics and tolerability of daptomycin at doses up to 12 milligrams per kilogram of body weight once daily in healthy volunteers

Affiliations
Clinical Trial

Pharmacokinetics and tolerability of daptomycin at doses up to 12 milligrams per kilogram of body weight once daily in healthy volunteers

Mark Benvenuto et al. Antimicrob Agents Chemother. 2006 Oct.

Abstract

Daptomycin, a novel lipopeptide, is bactericidal against a broad range of gram-positive strains, including methicillin- (MRSA) and vancomycin-resistant Staphylococcus aureus. Daptomycin is approved at 4 mg/kg of body weight given intravenously once daily for the treatment of complicated skin and skin structure infections and at 6 mg/kg for the treatment of S. aureus bloodstream infections (bacteremia), including right-sided endocarditis caused by methicillin-susceptible S. aureus and MRSA. The present study was designed to evaluate the multiple-dose pharmacokinetics and safety of daptomycin at doses of 6 to 12 mg/kg in healthy volunteers. Three cohorts of 12 subjects each were given daptomycin (10 mg/kg) or placebo once daily for 14 days, daptomycin (12 mg/kg) or placebo once daily for 14 days, or daptomycin (6 or 8 mg/kg) once daily for 4 days. Daptomycin produced dose-proportional increases in the area under the plasma concentration-time curve and in trough daptomycin levels and nearly dose-proportional increases in peak daptomycin concentrations. Other pharmacokinetic parameters measured on day 1 and at steady state were independent of the dose, including the half-life (approximately 8 h), weight-normalized plasma clearance (9 to 10 ml/h/kg), and volume of distribution (approximately 100 ml/kg). Plasma protein binding was 90% to 93% and was independent of the daptomycin concentration. Daptomycin did not produce electrocardiographic abnormalities or electrophysiological evidence of muscle or nerve toxicity. Daptomycin was well tolerated in subjects dosed with up to 12 mg/kg intravenously for 14 days. Doses of daptomycin higher than 6 mg/kg once daily may be considered in further studies to evaluate the safety and efficacy of daptomycin in difficult-to-treat infections.

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Figures

FIG. 1.
FIG. 1.
Plasma daptomycin (DAP) concentration-time curves on day 1 (A) and at steady state (day 4) (B).
FIG. 2.
FIG. 2.
Relationship between daptomycin dose and steady-state AUC in this study (6 to 12 mg/kg) and a previous phase 1 study by Dvorchik et al. (4 to 8 mg/kg) in healthy volunteers (5). The line shows a projection of dose proportionality over the dose range covered by these studies.

References

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    1. Cubist Pharmaceuticals. 2003. Cubicin (daptomycin for injection) prescribing information. Cubist Pharmaceuticals, Lexington, Mass.
    1. Cubist Pharmaceuticals. 2006. Cubicin (daptomycin for injection) prescribing information. Cubist Pharmaceuticals, Lexington, Mass.
    1. Dvorchik, B. H., D. Brazier, M. F. DeBruin, and R. D. Arbeit. 2003. Daptomycin pharmacokinetics and safety following administration of escalating doses once daily to healthy subjects. Antimicrob. Agents Chemother. 47:1318-1323. - PMC - PubMed

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