Major developments in research into the azole class of antifungal agents du
ring the 1990s have provided expanded options for the treatment of many opp
ortunistic and endemic fungal infections. Fluconazole and itraconazole have
proved to be safer than both amphotericin B and ketoconazole. Despite thes
e advances, serious fungal infections remain difficult to treat and resista
nce to the available drugs is emerging. This review describes present and f
uture uses of the currently available azole antifungal agents in the treatm
ent of systemic and superficial fungal infections and provides a brief over
view of the current status of in vitro susceptibility testing and the growi
ng problem of clinical resistance to the azoles. Use of the currently avail
able azoles in combination with other antifungal agents with different mech
anisms of action is likely to provide enhanced efficacy. Detailed informati
on on some of the second-generation triazoles being developed to provide ex
tended coverage of opportunistic endemic, and emerging fungal pathogens, as
well as those in which resistance to older agents is becoming problematic,
is provided.