The narrow therapeutic/toxic ratio of existing aminoglycosides has led
to a search for safer drugs of this class. Isepamicin is a semi-synth
etic aminoglycoside with a significantly low nephro as well as ototoxi
city in animals and which is expected to have a clinical efficacy comp
arable to that of amikacin. We therefore compared its antibacterial ac
tivity with amikacin against 817 recent clinical isolates of gram-posi
tive and gram-negative bacteria. The in vitro activity of isepamicin w
as comparable or slightly greater than amikacin against Staphylococcus
aureus and most Enterobacteriaceae. However, it was significantly mor
e inhibitory towards Serratia marcescens, Enterobacter and Klebsiella
pneumoniae.