POPular GUILTY PILOT: Genotype-guided Clopidogrel Monotherapy
Study Details
Study Description
Brief Summary
The goal of this pilot clinical trial is to test the safety and effectiveness of genotype-guided clopidogrel monotherapy in patients presenting with Non-ST-Segment Elevation Acute Coronary Syndrome (NSTE-ACS) who have undergone successful Percutaneous Coronary
Intervention (PCI). The main questions it aims to answer are:
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Is genotype-guided clopidogrel monotherapy effective in reducing ischemic risk during the first six months following successful PCI?
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Is genotype-guided clopidogrel monotherapy safe in terms of reducing bleeding risk during the first six months following successful PCI?
Participants will be given genotype-guided clopidogrel monotherapy after their successful PCI procedure and will be monitored for any bleeding or ischemic complications over the next six months.
Researchers will compare these results to the typical outcomes associated with traditional Dual antiplatelet therapy (DAPT) to see if genotype-guided clopidogrel monotherapy provides similar or improved protection from ischemic events, but with fewer bleeding complications.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
| Phase 2 |
Detailed Description
Rationale: Dual antiplatelet therapy (DAPT) consisting of aspirin and a P2Y12 inhibitor is the cornerstone of treatment in patients receiving coronary stent implantation, reducing the risk of stent thrombosis (ST), myocardial infarction (MI) and stroke. However, the need for aspirin is currently challenged as both technical and pharmaceutical advancements reduced atherothrombotic complications such as ST and MI after percutaneous coronary intervention (PCI) and DAPT is associated with bleeding complications. Single antiplatelet therapy (SAPT) after a 1-3 month period of DAPT demonstrated fewer bleeding complications with a similar level of ischemic complications. In addition, potent P2Y12 inhibitor monotherapy was deemed safe without any ST in a pilot study and is currently being investigated in a randomized controlled clinical trial. Since clopidogrel is equally effective in prevention of ischemic complications to ticagrelor and prasugrel in CYP2C19 extensive or ultra-rapid metabolizers, while causing less bleeding complications, this pilot study will explore the safety of genotype-guided clopidogrel monotherapy in CYP2C19 extensive or ultra-rapid metabolizers presenting with Non-ST-Segment Elevation Acute Coronary Syndrome (NSTE-ACS) undergoing successful PCI.
Hypothesis:
Genotype-guided clopidogrel monotherapy is safe in regards to bleeding and ischemic endpoints in NSTE-ACS patients undergoing successful PCI.
Objective:
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To assess ischemic risk (i.e. efficacy) of genotype-guided clopidogrel monotherapy during the first 6 months following successful PCI in NSTE-ACS patients.
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To assess bleeding risk (i.e. safety) of genotype-guided clopidogrel monotherapy during the first 6 months following successful PCI in NSTE-ACS patients.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Genotype guided arm In this study arm, patients with Non-ST-Segment Elevation Acute Coronary Syndrome (NSTE-ACS) who are extensive or ultra-rapid metabolizers as per their CYP2C19 genotype and have undergone successful percutaneous coronary intervention (PCI) will receive a genotype-guided monotherapy. The intervention will be clopidogrel, a potent P2Y12 inhibitor, administered in accordance with the patient's specific genotype. Clopidogrel following PCI will be given with an initial loading dose (300-600mg orally), followed by a maintenance dose of 75mg daily for a defined period, at least 6 months. |
Drug: Clopidogrel
See arm description earlier.
|
Outcome Measures
Primary Outcome Measures
- Primary efficacy endpoint [6 months]
A composite endpoint consisting of all-cause mortality, myocardial infarction, probable and definite Stent Thrombosis and ischemic stroke (the first event that occurs will be counted for this composite endpoint)
- Primary safety endpoint [6 months]
Composite endpint consisting of major or clinically relevant non-major bleeding (BARC type 2, 3 or 5 bleeding)
Secondary Outcome Measures
- Mortality [3 and 6 months]
all-cause mortality
- Myocardial infarction [3 and 6 months]
Myocardial infarction
- Stent thrombosis [3 and 6 months]
Probable and definite Stent Thrombosis
- Ischemic stroke [3 and 6 months]
ischemic stroke
- Major bleeding [3 and 6 months]
BARC 3 or 5 bleeding
- Major bleeding [3 and 6 months]
BARC 3 bleeding
- Clinically relevant non-major bleeding [3 and 6 months]
BARC 2 bleeding
Eligibility Criteria
Criteria
Inclusion Criteria:
Patients aged 18 years or older are eligible for inclusion if all of the following criteria are met:
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Clinical diagnosis of NSTE-ACS (i.e. NSTEMI or unstable angina)
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Successful PCI (according to the treating physician) with implantation of new generation drug eluting stents.
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CYP2C19 extensive or ultra-rapid metabolizer
Exclusion Criteria:
A potential subject who meets any of the following criteria will be excluded from participation in this study:
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CYP2C19 poor or intermediate metabolizer
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Known allergy or contraindication for aspirin or clopidogrel.
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Concurrent use of oral anticoagulants (e.g. because of atrial fibrillation)
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Ongoing indication for DAPT at admission (e.g. due to recent PCI or ACS)
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High-risk features for PCI including left main disease, chronic total occlusion, bifurcation lesion requiring 2-stent treatment, saphenous or arterial graft lesion, severely calcified lesion requiring the use of the Rotablator system, ≥3 treated vessels, ≥ 3 stents implanted and total stent length >60 mm
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Recent stroke, transient ischemic attack (TIA) or intracranial bleeding
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Severe hepatic impairment (Child Pugh class C)
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Planned surgical intervention within 6 months of PCI
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Patients requiring staged procedure (to avoid heterogeneity in the duration of pharmacological treatment between index and staged procedures)
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Pregnant or breastfeeding women at time of enrolment
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Participation in another trial with an investigational drug or device
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | St. Antonius Hospital | Nieuwegein | Utrecht | Netherlands |
Sponsors and Collaborators
- St. Antonius Hospital
Investigators
- Study Director: Ashley Verburg, MD, St. Antonius Hospital
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- NL82555.100.22