D. Felmingham et al., IN-VITRO ACTIVITY OF TROVAFLOXACIN, A NEW FLUOROQUINOLONE, AGAINST RECENT CLINICAL ISOLATES, Journal of antimicrobial chemotherapy, 39, 1997, pp. 43-49
Trovafloxacin (CP-99,219) was very active against Gram-negative specie
s examined including Haemophilus influenzae, Moraxella catarrhalis, Le
gionella spp., Neisseria spp. and Escherichia coli (MIC(90)s less than
or equal to 0.03 mg/L). In general trovafloxacin was twice as active
as ofloxacin but only half as active as ciprofloxacin against Gram-neg
ative species. Trovafloxacin was active against Gram-positive organism
s, including Staphylococcus aureus, Streptococcus pneumoniae, Streptoc
occus pyogenes and Enterococcus faecalis (MIC(90)s less than or equal
to 0.25 mg/L). Against these organisms activity was eight to 16 times
greater for trovafloxacin than for either ofloxacin or ciprofloxacin.
In addition, Chlamydia spp., Mycoplasma spp. and Ureaplasma urealyticu
m were eight to 16 times more susceptible to trovafloxacin than to eit
her ofloxacin or ciprofloxacin. These in-vitro data show that trovaflo
xacin is a broad-spectrum fluoroquinolone with greater activity agains
t clinically important Gram-positive species compared with ofloxacin o
r ciprofloxacin.