In vitro activity of trovafloxacin against Chlamydia pneumoniae

Abstract

The in vitro susceptibilities of 12 strains of Chlamydia pneumoniae to a new quinolone, trovafloxacin, and ofloxacin, doxycycline, erythromycin, and azithromycin were determined. The activity of trovafloxacin was similar to that of ofloxacin, with a MIC at which 90% of the isolates are inhibited and a minimal concentration at which 90% of the isolates are killed of 1.0 μg/ml, but trovafloxacin was less active than doxycycline, erythromycin, and azithromycin.