Drug intelligence / Profile preview

SUBA itraconazole

Development stage
Phase 3
Lead developer
Mayne Pharma
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules
Administration
Oral
01

Overview

SUBA itraconazole is a novel oral formulation of the antifungal agent itraconazole that utilizes "super bioavailability" (SUBA) technology. This technology disperses the active drug in a pH-dependent polymeric matrix to enhance dissolution and intestinal absorption compared to conventional crystalline formulations. The result is improved and more consistent bioavailability with less interpatient variability and reduced food or acid effect on absorption. Mechanistically, like other triazole antifungals, it inhibits fungal cytochrome P450 14α-demethylase (lanosterol 14α-demethylase), thereby blocking ergosterol synthesis essential for fungal cell membrane integrity. It is FDA-approved for the treatment of systemic mycoses including blastomycosis, histoplasmosis (including chronic cavitary pulmonary disease and disseminated non-meningeal forms), and aspergillosis in patients intolerant of or refractory to amphotericin B therapy. It is also used off-label for dermatophytosis and onychomycosis[2][3][5][7][8].

Brand names
TolsuraLozanoc
Other names
super-bioavailable itraconazoleSB ITZ
02

Targets

CYP51A1 (Sterol 14α-demethylase)

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