In this study, the potency of faropenem (SUN 5555, Sy 5555, ALP-201 or WY-49605), a new oral penem, characterized by a broad spectrum of antimicrobial activity [1-6], was explored against a large collection of lower respiratory tract pathogens in comparison with other oral drugs. Since production of p-lactamases in closed-space infections is known to represent a possible cause of therapeutic failure [7], the ability of faropenem to kill P-lactamase-producing Moraxella catarrhah and Haemophilus injuenzae in a dynamic bactericidal model was also explored.Pathogens were represented by: 503 Streptococcus pneumoniae strains, including 29 low-level (MIC 0.12-1 mg/L) and high-level (MIC >2 mg/L) penicillinresistant strains; 310 H . inzuenzae strains (including 14 p-lactamase producers); and 63 M. catarrhalis strains (including 48 P-lactamase producers). All pathogens were consecutive (non-duplicate patients) microorganisms isolated from 1993 to 1996 at the Institute of Microbiology, Genoa, Italy.Faropenem, cefpodoxime and ofloxacin were obtained from Roussel Uclaf, Paris, France, while the other drugs (arnoxycillin, co-clavulanate, cefpodoxime, cefixime, cefuroxime, loracarbef, ofloxacin, ciprofloxacin, erythromycin, clarithromycin and azithromycin) were supplied by their respective manufacturers. Sterile stock solutions of the antibiotics were prepared from the standard reference powders in accordance with the instructions received.MICs of faropenem and of the other drugs were determined by using the methods suggested by the