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Voriconazole preemptive genotyping strategy

Instituto de Investigación Hospital Universitario La Paz · FDA-approved active Small molecule

A pharmacogenomic strategy that uses CYP2C19 genotyping to optimize voriconazole dosing and reduce adverse events in individual patients.

A pharmacogenomic strategy that uses CYP2C19 genotyping to optimize voriconazole dosing and reduce adverse events in individual patients. Used for Invasive aspergillosis, Candidemia and other Candida infections, Esophageal candidiasis.

At a glance

Generic nameVoriconazole preemptive genotyping strategy
SponsorInstituto de Investigación Hospital Universitario La Paz
Drug classTriazole antifungal with pharmacogenomic optimization
TargetCYP2C19 enzyme (pharmacogenomic target); fungal lanosterol 14α-demethylase (therapeutic target)
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved

Mechanism of action

Voriconazole is a triazole antifungal agent whose metabolism is highly dependent on CYP2C19 enzyme activity, which varies significantly among individuals due to genetic polymorphisms. By preemptively genotyping patients for CYP2C19 variants (poor metabolizers, intermediate metabolizers, extensive metabolizers, and ultra-rapid metabolizers), clinicians can adjust voriconazole dosing to maintain therapeutic drug levels while minimizing toxicity. This personalized medicine approach reduces the risk of subtherapeutic exposure or drug accumulation-related adverse effects.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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