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Dalbavancin: A novel lipoglycopeptide antibacterial

Journal

PHARMACOTHERAPY
Volume 26, Issue 7, Pages 908-918

Publisher

WILEY
DOI: 10.1592/phco.26.7.908

Keywords

dalbavancin; BI 397; lipoglycopeptide; glycopeptide; methicillin-resistant Staphylococcus aureus; MRSA; gram-positive bacteria

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Dalbavancin is a new lipoglycopeptide antibacterial possessing in vitro activity against a variety of gram-positive pathogens. Against methicillin-susceptible and methicillin-resistant Staphylococcus aureus, it has demonstrated favorable minimum inhibitory concentration ranges compared with those of currently available agents. Dalbavancin is highly protein bound (> 90%), which may contribute to its prolonged half-life of 149-300 hours. Because of this long half-life, once-weekly dosing strategies have been used in clinical trials. Efficacy and tolerability have been demonstrated in a wide variety of animal infection models. Clinical success and safety have been shown in phase 11 and III trials for skin and soft-tissue infections and a phase 11 trial for catheter-related bloodstream infections. In these trials with vancomycin, linezolid, and various beta-lactams as comparators, comparable results have been reported. The results of further phase III trials are anxiously awaited and will more clearly define the clinical role of this novel agent.

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