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Personalized DAPT duration

Federico II University · FDA-approved active Small molecule

Personalized DAPT duration tailors the length of dual antiplatelet therapy (aspirin + P2Y12 inhibitor) to individual patient risk factors rather than using a fixed treatment duration.

Personalized DAPT duration tailors the length of dual antiplatelet therapy (aspirin plus P2Y12 inhibitor) to individual patient risk factors rather than using a fixed treatment duration. Used for Acute coronary syndrome with percutaneous coronary intervention and stent placement, Stable coronary artery disease with percutaneous coronary intervention and stent placement.

At a glance

Generic namePersonalized DAPT duration
SponsorFederico II University
ModalitySmall molecule
Therapeutic areaCardiovascular
PhaseFDA-approved

Mechanism of action

This is a treatment strategy rather than a single drug entity. It involves customizing the duration of dual antiplatelet therapy based on patient-specific bleeding and ischemic risk profiles, typically assessed through clinical scoring systems or biomarkers. The approach aims to optimize the balance between reducing stent thrombosis risk and minimizing bleeding complications by individualizing therapy duration beyond standard 12-month protocols.

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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