1887

Abstract

is the most common non-gonococcal aetiology of septic arthritis. The efficacy of iclaprim against LS-1, a clinical strain identified from a patient with septic arthritis, was studied in MF1 mice to evaluate the activity of iclaprim, which is in clinical development, in preventing joint infections. Iclaprim (2.5–80 mg kg ) administered as a single dose via the tail vein reduced the incidence of septic arthritis and mortality in an experimental murine model of septic arthritis.

  • This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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2019-09-01
2024-05-10
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