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Telavancin

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Abstract

  • ▴ Telavancin is the first available lipoglycopeptide antibacterial agent. It is active against Gram-positive bacteria, including meticillin/oxacillin-resistant Staphylococcus aureus (MRSA) strains associated with complicated skin and skin structure infections (cSSSIs).

  • ▴ In randomized, double-blind trials, intravenous telavancin 10 mg/kg once daily (administered as a 1-hour infusion) was effective in the treatment of adult patients with cSSSIs, including those with infections caused by MRSA, as shown by clinical cure rates in clinically evaluable, all-treated and microbiologically evaluable populations at the test-of-cure (TOC) visit.

  • ▴ Telavancin 10 mg/kg once daily was noninferior to intravenous vancomycin 1 g every 12 hours, with clinical cure rates of 88% versus 87% at the TOC visit in pooled data from the clinically evaluable population (n=1489) of two phase III trials.

  • ▴ Pooled clinical cure rates in telavancin recipients at the TOC visit were also not significantly different from those in vancomycin recipients in the all-treated or microbiologically evaluable populations, including microbiologically evaluable subgroups with baseline infections caused by MRSA, meticillin-susceptible S. aureus or other Gram-positive pathogens.

  • ▴ Telavancin was generally well tolerated in patients with cSSSIs, with most adverse events being of mild or moderate severity.

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Acknowledgements and Disclosures

The manuscript was reviewed by: G.R. Corey, Division of Infectious Diseases, Duke University Medical Center, Durham, North Carolina, USA; J.M. Embil, Section of Infectious Diseases, Department of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada; F. Van Bambeke, Unité de pharmacologie cellulaire et moléculaire, Université catholique de Louvain, Brussels, Belgium.

The preparation of this review was not supported by any external funding.

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Correspondence to Katherine A. Lyseng-Williamson.

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Lyseng-Williamson, K.A., Blick, S.K.A. Telavancin. Drugs 69, 2607–2620 (2009). https://doi.org/10.2165/10481380-000000000-00000

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