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Dalbavancin: a Novel Once-Weekly Lipoglycopeptide Antibiotic
Author(s) -
Louis D. Saravolatz,
Marianne Billeter,
Marcus Zervos,
A. Y. Chen,
J. R. Dalovisio,
Changa Kurukularatne
Publication year - 2008
Publication title -
clinical infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.44
H-Index - 336
eISSN - 1537-6591
pISSN - 1058-4838
DOI - 10.1086/526772
Subject(s) - dalbavancin , medicine , linezolid , vancomycin , antibiotics , staphylococcus aureus , dosing , microbiology and biotechnology , pharmacology , biology , bacteria , genetics
The increasing prevalence of drug-resistant gram-positive cocci, such as methicillin-resistant Staphylococcus aureus, has underscored the need for new agents for the treatment of this type of infection. Dalbavancin, a new lipoglycopeptide, has the desirable characteristics of increased in vitro activity, compared with vancomycin, for most gram-positive pathogenic bacteria, as well as an extremely long half-life, permitting once-weekly intravenous dosing. Clinical studies comparing linezolid with 2 doses of dalbavancin have shown comparable efficacy for the treatment of skin and soft-tissue infection. Dalbavancin has also proven to be effective for therapy of catheter-related bloodstream infections. It has an excellent safety profile in studies to date. Dalbavancin will likely have a significant role in outpatient intravenous therapy for patients with potentially serious drug-resistant gram-positive coccal infections.

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