A Pharmacodynamic Study of a Personalized Strategy for P2Y12 Inhibition Versus Ticagrelor in Reducing Ischemic and Bleeding Risk

Last updated: October 3, 2018
Sponsor: Ottawa Heart Institute Research Corporation
Overall Status: Completed

Phase

2/3

Condition

Myocardial Ischemia

Open Heart Surgery

Chest Pain

Treatment

N/A

Clinical Study ID

NCT02044146
20130601
  • Ages 18-75
  • All Genders

Study Summary

In patients with heart attacks, the treatment of choice is to restore blood flow with percutaneous coronary intervention (PCI) (use of stents (metal meshes) to open blockages). After PCI, the standard drug treatment includes aspirin and clopidogrel. These medications block full function of the platelet cells, which are responsible for clotting. Despite their use, patients after PCI are at risk for heart attacks, sudden clotting of stents or death. A major contributor may be resistance to clopidogrel. New more potent drugs, which can overcome the resistance, are now available; however, they come with an increase chance of severe bleeding and costs. An ideal solution would be to identify at-risk patients and selectively treat them with more potent drugs, while lower-risk patients continue with clopidogrel. This type of strategy (personalized strategy) would decrease heart attacks and death (compared to clopidogrel), while also preventing bleeding complications (compared to treating all patients with the new drugs).

Of resistant patients, many carry genes (inherited units) that prevent proper absorption of clopidogrel. Our group has developed and tested a new bedside genetic test, which identifies carriers of at-risk genes. However, this technique alone does not identify all at-risk patients. Consequently, we have now devised a novel tool, which combines genetics with patient characteristics to identify high-risk patients.

The present study combines this new tool into a strategy for personalized treatment. Patients with heart attacks who undergo PCI will be randomly assigned to 1 of 3 strategies: a) new personalized strategy, b) clopidogrel strategy (previous standard drug) or c) ticagrelor strategy (stronger approved drug). The function of the platelet cells will be measured at 1 month to determine potential benefits. Evaluation of this new personalized strategy is important for improving patient outcomes after PCI. The hypothesis is that patients receiving a personalized strategy will have decrease risk for future heart attacks and bleeding.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patients: age >18 yrs, < 75yrs

-> 60 kg ( since March 2015 age >75 and < 60 kg eligible - but prasugrel reduced to 5mg daily if randomized to personalized therapy arm)

  • NSTEMI undergoing PCI will be eligible

Exclusion

Exclusion Criteria:

  • Patients will be excluded if they have: i) a contra-indication for clopidogrel orprasugrel or ticagrelor (as per monograph), ii) have an intolerance to aspirin, iii) haveabsolute requirement for ticagrelor or prasugrel (e.g. stent thrombosis, allergic reactionto clopidogrel), iv) requirement for anti-coagulation treatment, v) a history of stroke,TIA or intracranial hemorrhage , vi) a platelet count < 100,000/μl, vii) a known bleedingdiathesis, viii) hematocrit <30% or >52%, ix) severe liver dysfunction, x) renalinsufficiency (creatinine clearance < 30ml/min), xi) adjuvant therapy with a glycoproteinIIbIIIa inhibitor.

Study Design

Total Participants: 120
Study Start date:
September 01, 2014
Estimated Completion Date:
June 30, 2017

Connect with a study center

  • University of Ottawa Heart Institute

    Ottawa, Ontario K1Y4W7
    Canada

    Site Not Available

  • Montreal Heart Institute

    Montreal, Quebec H1T1C8
    Canada

    Site Not Available

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