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Ticlopidine and itraconazole

Turku University Hospital · FDA-approved active Small molecule

This is a combination of ticlopidine (a platelet aggregation inhibitor) and itraconazole (an antifungal agent), used together to manage thrombotic and fungal complications.

This is a combination of ticlopidine (a platelet aggregation inhibitor) and itraconazole (an antifungal agent), used together to manage thrombotic and fungal complications. Used for Thrombotic prevention (ticlopidine component), Fungal infection treatment (itraconazole component).

At a glance

Generic nameTiclopidine and itraconazole
SponsorTurku University Hospital
Drug classAntiplatelet agent + Antifungal agent
TargetADP receptor (P2Y12) for ticlopidine; Fungal CYP51 for itraconazole
ModalitySmall molecule
Therapeutic areaCardiovascular / Infectious Disease
PhaseFDA-approved

Mechanism of action

Ticlopidine inhibits platelet aggregation by blocking ADP-induced platelet activation, reducing thrombotic events. Itraconazole is a triazole antifungal that inhibits fungal cytochrome P450-dependent lanosterol demethylase, preventing ergosterol synthesis. The combination addresses both antiplatelet and antifungal therapeutic needs, though this pairing is unusual and likely reflects a specific clinical scenario rather than a synergistic mechanism.

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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