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. 2012 Mar 11;2012:956962. doi: 10.1155/2012/956962

Table 6.

Ongoing studies assessing pharmacogenomics and antiplatelet therapy.

Study Number of patients Patient population Therapy Primary endpoint
GIFT NA All-comers undergoing PCI Tailored clopidogrel versus standard clopidogrel according to platelet reactivity and genetic type Residual platelet activity
TARGET-PCI 1,500 Nonemergent PCI Tailored with clopidogrel and prasugrel to results of platelet reactivity and genetic type MACE
CLOVIS-2 120 Post-MI Clopidogrel 300 mg versus Clopidogrel 600 mg in 2 genetic CYP2C19 types Inhibition of residual platelet activity 6 hours following clopidogrel
PREDICT 42 Stable CAD Those with high residual platelet activity on clopidogrel and genotyped for CYP2C19 treated with double dose clopidogrel Change in residual platelet activity
GeCCO 14,600 Recent ACS Genotype-guided comparison of clopidogrel in extensive metabolizers and prasugrel Cardiovascular death, nonfatal MI, or nonfatal stroke

GIFT: Genotype Information and Functional Testing; TARGET-PCI: Thrombocyte Activity Reassessment and Genotyping for PCI; CLOVIS-2: Clopidogrel and response Variability Investigation Study 2; PREDICT: Pilot Study on the Effect of High Clopidogrel Maintenance Dosing; GeCCO: Genotype Guided Comparison of Clopidogrel and Prasugrel Outcomes Study; PCI: percutaneous coronary intervention; MI: myocardial infarction; CAD: coronary artery disease; ACS: acute coronary syndrome; MACE: major adverse cardiovascular event.