CLOVIS2: Clopidogrel and Response Variability Investigation Study 2
Study Details
Study Description
Brief Summary
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.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
| Phase 3 |
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
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Maximum platelet aggregation instead of IRPA
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RPA with 5µM and 50 µM of ADP
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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
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Relationship between active metabolites concentration and IRPA
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Relationship between active metabolites and dose of clopidogrel
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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 2C192 by anova Area under the curve of the production of active metabolites with respect to the presence of the genetic variant 2C192 Agenda :November 2008 (inclusion of first patient) to december 2009 (analysis of the data)
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Active Comparator: 1 patients homozygous for the 2C19*1 genetic variant |
Drug: clopidogrel
comparison of two loading strategies of clopidogrel (300mg vs 900mg) in the two genetic profiles
|
| Experimental: 2 carriers of the 2C19*2 genetic variant (homozygous or heterozygous) |
Drug: clopidogrel
comparison of two loading strategies of clopidogrel (300mg vs 900mg) in the two genetic profiles
|
Outcome Measures
Primary Outcome Measures
- Inhibition of residual platelet activity 6 hours after a loading dose of clopidogrel [6 hours]
Secondary Outcome Measures
- Maximum platelet aggregation instead of IRPA [during the study]
- RPA with 5µM and 50 µM of ADP [during the study]
- 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 [H0, H1, H2, H6]
- Relationship between active metabolites concentration and IRPA [during the study]
- Relationship between active metabolites and dose of clopidogrel [during the study]
Eligibility Criteria
Criteria
Inclusion Criteria:
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Age > 18
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Male gender
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Included in the AFIJI registry
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No high bleeding risk profile
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No recent history of acute coronary syndrome (< 3 months)
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Written informed consent obtained
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Genotype CYP2C19 : *1/*1, *1/*2 ou *2/*2
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Genotype P2Y12 : H1/H1 ou H1/H2
Exclusion Criteria:
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Female gender
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Patient with a contraindication to clopidogrel
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Patient who has received a loading dose of clopidogrel in the past 7 days
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Patient treated with ticlopidine or GP2B/3A receptor antagonist prior to loading
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Non compliance
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Génotype P2Y12 : H2/H2.
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Patient treated with drugs interacting with platelet aggregation (NSAID, persantine, serotonin inhibitors )
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Patient treated with drugs interacting 2C19
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Not affiliated to the national health insurance
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Patient participating to another randomized study
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Hopital la Pitié-Salpétrière Institut de cardiologie | Paris | France | 75013 |
Sponsors and Collaborators
- Assistance Publique - Hôpitaux de Paris
- Institut National de la Santé Et de la Recherche Médicale, France
Investigators
- Principal Investigator: Jean-Philippe Collet, MD, Assistance Publique - Hôpitaux de Paris
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- P070117