Drug intelligence / Profile preview

olodaterol + fluconazole

Development stage
Unknown
Lead developer
Boehringer Ingelheim
Modality
Small Molecules
Administration
Inhalation, Oral
01

Overview

Olodaterol + fluconazole is a drug combination primarily utilized in clinical pharmacology studies to evaluate drug-drug interactions. Olodaterol is a highly selective, long-acting beta2-adrenergic agonist (LABA) developed by Boehringer Ingelheim for the treatment of chronic obstructive pulmonary disease (COPD). Fluconazole is a triazole antifungal agent that acts as a potent inhibitor of the cytochrome P450 enzyme CYP2C9 and a moderate inhibitor of CYP2C19. Because olodaterol is partially metabolized by these enzymes, the combination is studied to determine if fluconazole-mediated inhibition increases the systemic exposure or alters the safety profile of olodaterol. There is no commercially available fixed-dose combination of these two agents.

Other names
olodaterol and fluconazole
02

Targets

CYP2C9 (Cytochrome P450 family 2 subfamily C member 9)ADRB2 (β2)CYP51A1 (Sterol 14α-demethylase)

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