Drug intelligence / Profile preview

BI 894416 + itraconazole

Development stage
Phase 1
Lead developer
Boehringer Ingelheim
Modality
Small Molecules
Administration
Oral
01

Overview

**BI 894416 + itraconazole** is a combination of a clinical-stage investigational drug (BI 894416, developed by Boehringer Ingelheim) and a widely used antifungal agent, **itraconazole**. While specific details on BI 894416 are limited in public sources, itraconazole is a broad-spectrum triazole antifungal. It inhibits fungal cell membrane synthesis by blocking lanosterol 14-alpha demethylase, an enzyme essential for converting lanosterol to ergosterol, thereby compromising cell membrane integrity[2][5]. Itraconazole is used in the treatment of systemic and superficial fungal infections. This combination may be used in clinical trials to study drug-drug interactions or the effect of CYP3A4 inhibition on the pharmacokinetics of BI 894416, since itraconazole is a potent inhibitor of CYP3A4 and drug transporters like P-glycoprotein[1][5].

Other names
BI 894416BI894416BI-894416itraconazole
02

Targets

CYP3A4 (Cytochrome P450 3A4)CYP51A1 (Sterol 14α-demethylase)ABCB1 (P-glycoprotein)PIK3R1 (Phosphatidylinositol 4-phosphate 3-kinase regulatory subunit alpha)STAT3 (Signal Transducer and Activator of Transcription 3)ABCG2 (Breast cancer resistance protein)

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