Clopidogrel and Response Variability Investigation Study 2

Condition(s) targeted: Coronary Artery Disease

Intervention: clopidogrel (Drug)

Phase: Phase 3

Status: Recruiting

Sponsored by: Assistance Publique - Hôpitaux de Paris

Official(s) and/or principal investigator(s):
Jean-Philippe Collet, MD, Principal Investigator, Affiliation: Assistance Publique - Hôpitaux de Paris

Overall contact:
Jean-Philippe Collet, MD, Phone: (33) 1 42 16 30 07, Email: Jean-philippe.collet@psl.aphp.fr

To evaluate the role of the genetic variant 2C19*2 on the pharmacodynamic response as assessed by optical aggregometry and on the pharmacokinetic response as assessed by measuring active metabolites following an oral administration of a loading dose of 300/900mg of clopidogrel in patients with established coronary artery disease.

Official title: Effect of the Genetic Variant 2C19*2 on Clopidogrel Biological Response in Patients With Premature Coronary Artery Disease

Study design: Treatment, Randomized, Open Label, Dose Comparison, Crossover Assignment, Pharmacokinetics/Dynamics Study

Primary outcome: Inhibition of residual platelet activity 6 hours after a loading dose of clopidogrel

Secondary outcome:

Maximum platelet aggregation instead of IRPA

RPA with 5µM and 50 µM of ADP

3. Measure of clopidogrel and its active metabolites (carboxylated and thiol) at different time points following the loading dose (H0, H1, H2 ,H6) with respect to the presence of the genetic variant CYP2C19*2

Relationship between active metabolites concentration and IRPA

Relationship between active metabolites and dose of clopidogrel

Detailed description: Rationale : Clopidogrel is a specific and irreversible of the P2Y12 platelet receptor leading to an inhibition of platelet aggregation. Clopidogrel is a prodrug that must be converted into an active metabolite that selectively and irreversibly binds to the P2Y12 platelet membrane receptor. As a consequence, a loading dose of 300 mg is necessary in percutaneous coronary intervention and in acute coronary syndrome, situations which require a rapid inhibition of platelet aggregation due to the high thrombotic risk.

High platelet reactivity on clopidogrel may be due to various reasons including polymorphism in the gene encoding the cytochrome P-450 2C19 enzyme (CYP2C19) which has been shown to contribute to the variability of platelet response to clopidogrel. CYP2C19 is a key enzyme in this activation process and our group was the first to describe an association between the presence of the loss of function CYP2C19 681G>A polymorphism (also called *2) with lower clopidogrel responsiveness in healthy subjects.

Poor responsiveness to clopidogrel has become a major concern given acute recurrent events following stent placement.

Objective : To evaluate the role of the genetic variant 2C19*2 on the pharmacodynamic response as assessed by optical aggregometry and on the pharmacokinetic response as assessed by measuring active metabolites following an oral administration of a loading dose of 300/900mg of clopidogrel in patients with established coronary artery disease.

Target population :Patients of less than 45 years of age and who survived a MI and enrolled in the AFIJI multicenter registry (Appraisal of risk Factors in young Ischemic patients Justifying aggressive Intervention).

Primary end-point :Comparison of inhibition of the intensity of residual platelet aggregation (IRPA) measured 6 minutes after induction by 20 μmol/L following 300mg or 900 mg of clopidogrel with respect to the presence of the genetic variant CYP2C19*2

1. Maximum platelet aggregation instead of IRPA

2. RPA with 5µM and 50 µM of ADP

3. Measure of clopidogrel and its active metabolites (carboxylated and thiol) at different time points following the loading dose (H0, H1, H2 et H6) with respect to the presence of the genetic variant CYP2C19*2

4. Relationship between active metabolites concentration and IRPA

5. Relationship between active metabolites and dose of clopidogrel

6. Comparison of 300mg vs 900mg on IRPA in the whole population irrespective of the genetic variant

Statistical analysis :Comparison of IRPA with respect to the presence of the genetic variant 2C19*2 by anova Area under the curve of the production of active metabolites with respect to the presence of the genetic variant 2C19*2 Agenda :November 2008 (inclusion of first patient) to december 2009 (analysis of the data)

Minimum age: 18 Years. Maximum age: 75 Years. Gender(s): Male.

Criteria:

Inclusion Criteria:

- Age > 18

- Male gender

- Included in the AFIJI registry

- No high bleeding risk profile

- No recent history of acute coronary syndrome (< 3 months)

- Written informed consent obtained

- Genotype CYP2C19 : *1/*1, *1/*2 ou *2/*2

- Genotype P2Y12 : H1/H1 ou H1/H2

Exclusion Criteria:

- Female gender

- Patient with a contraindication to clopidogrel

- Patient who has received a loading dose of clopidogrel in the past 7 days

- Patient treated with ticlopidine or GP2B/3A receptor antagonist prior to loading

- Non compliance

- Génotype P2Y12 : H2/H2.

- Patient treated with drugs interacting with platelet aggregation (NSAID, persantine,

serotonin inhibitors )

- Patient treated with drugs interacting 2C19

- Not affiliated to the national health insurance

- Patient participating to another randomized study

Jean-Philippe Collet, MD, Phone: (33) 1 42 16 30 07, Email: Jean-philippe.collet@psl.aphp.fr

Hopital la Pitié-Salpétrière Institut de cardiologie, Paris 75013, France; Recruiting
Jean-Philippe Collet, MD, Phone: (33) 1 42 16 30 07, Email: Jean-philippe.collet@psl.aphp.fr
Jean-Philippe Collet, MD, Principal Investigator
Gilles Montalescot, MD, PhD, Sub-Investigator

Starting date: October 2008
Ending date: December 2009
Last updated: January 13, 2009