Two open crossover studies were conducted to investigate the effects o
f food or concomitant treatment with the histamine H-2-receptor antago
nist famotidine on the pharmacokinetics of the new fluoroquinolone gre
pafloxacin. Each study involved 16 healthy male volunteers. In the fir
st study, participants received grepafloxacin 600mg, either after fast
ing or after consumption of a standard high-fat meal. There were no si
gnificant differences in any pharmacokinetic parameter under the fasti
ng or nonfasting conditions. In the second study, participants receive
d grepafloxacin 400mg, either alone or after infusion of famotidine 20
mg; additional doses of famotidine were given, if necessary, to mainta
in intragastric pH above 6. Famotidine treatment had no significant ef
fect on grepafloxacin pharmacokinetics. The results of these studies i
ndicate that neither food nor the elevation of gastric pH influence th
e absorption or bioavailability of grepafloxacin. Therefore, grepaflox
acin can be administered with or without food.