Candida albicans is responsible for most fungal infections in humans. Fluco
nazole is well established as a first-line management option for the treatm
ent and prophylaxis of localized and systemic C. albicans infections. Fluco
nazole exhibits predictable pharmacokinetics and is effective, well tolerat
ed and suitable for use in most patients with C. albicans infections, inclu
ding children, the elderly and those with impaired immunity. Prophylactic a
dministration of fluconazole can help to prevent fungal infections in patie
nts receiving cytotoxic cancer therapy. The increasing use of fluconazole f
or the long-term prophylaxis and treatment of recurrent oral candidosis in
AIDS patients has led to the emergence of C. albicans infections that are n
ot responsive to conventional doses. Second-line therapy with a wider spect
rum anti-fungal, such as itraconazole, should be sought if treatment with f
luconazole fails. A solution formulation of itraconazole has recently been
introduced to overcome the poor and variable absorption of its original cap
sule formulation. Efficacy and tolerability studies in HIV-positive or immu
nocompromised patients with C. albicans infections have shown that, althoug
h itraconazole solution is as effective as fluconazole, it is less well tol
erated as first-line therapy. Itraconazole solution can be effective in AID
S patients with C. albicans infections that are non-responsive to fluconazo
le. No efficacy or tolerability data are available on the use of itraconazo
le solution in children or the elderly.