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Antithrombotic Effects of Ticagrelor Versus Clopidogrel

Primary Purpose

Acute Coronary Syndrome

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Ticagrelor + ASA + Bivalirudin
Clopidogrel + ASA + Bivalirudin
Sponsored by
Juan J Badimon
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Coronary Syndrome focused on measuring Antiplatelet, ticagrelor, clopidogrel, bivalirudin, thrombosis

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Male or female volunteers between 18 and 65 years old.
  • Body mass index (BMI) 18 - 30 kg/m2 inclusive.
  • Healthy as assessed by a detailed medical history and physical examination.
  • Laboratory est results within the normal range.
  • Ability to provide signed informed consent.

Exclusion Criteria:

  • History of clinically relevant disease, bleeding, acute infectious disease or signs of acute illness.
  • Allergy or hypersensitivity to aspirin or thienopyridines, or atopy diagnosed by a physician.
  • Use of medication within one month prior to study drug administration.
  • History of drug abuse or alcohol consumption >20 g/day.
  • Inability to abstain from intensive muscular effort or sport competition.
  • Loss of >400 mL blood or blood donation within 3 months.
  • Positive serology for hepatitis B (HBs Ag) or hepatitis C.
  • Conditions associated with hemorrhagic risk.
  • Positive pregnancy test.

Sites / Locations

  • Icahn School of Medicine at Mount Sinai

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Ticagrelor + ASA + Bivalirudin

Clopidogrel + ASA + Bivalirudin

Arm Description

Single loading dose of Ticagrelor (180 mg given as two 90 mg tablets), plus single dose of ASA (one 81 mg tablet) + bivalirudin administered as 0.75 mg/kg IV bolus followed by 1.75 mg/kg/hour for 1 hour.

Single loading dose of Clopidogrel (600 mg given as two 300 mg tablets), plus single dose of ASA (one 81 mg tablet) + bivalirudin administered as 0.75 mg/kg IV bolus followed by 1.75 mg/kg/hour for 1 hour.

Outcomes

Primary Outcome Measures

Platelet-thrombus Formation in an ex Vivo Model of Thrombosis
Change in thrombus size at 1 hour as compared to Pre-treatment baseline, where a positive change represents a decrease in thrombus size.
Platelet-thrombus Formation in an ex Vivo Model of Thrombosis
Change in thrombus size at 24 hours as compared to Pre-treatment baseline, where a positive change represents a decrease in thrombus size.

Secondary Outcome Measures

Platelet Reactivity
Platelet reactivity measured by VerifyNowP2Y12 assay measuring percent inhibition
Platelet Reactivity
Platelet reactivity measured by VerifyNowP2Y12 assay measuring percent inhibition
Platelet Reactivity
Platelet reactivity measured by VerifyNowP2Y12 assay measuring percent inhibition
Blood Thrombogenicity
Coagulation times, assessed using the ROTEM thromboelastometry
Blood Thrombogenicity
Coagulation times, assessed using the ROTEM thromboelastometry
Blood Thrombogenicity
Coagulation times, assessed using the ROTEM thromboelastometry

Full Information

First Posted
July 13, 2012
Last Updated
June 1, 2016
Sponsor
Juan J Badimon
Collaborators
AstraZeneca
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1. Study Identification

Unique Protocol Identification Number
NCT01642238
Brief Title
Antithrombotic Effects of Ticagrelor Versus Clopidogrel
Official Title
Randomized, Crossover Study of the Antithrombotic Effects of Ticagrelor Plus Aspirin Versus Clopidogrel Plus Aspirin When Administered With Bivalirudin
Study Type
Interventional

2. Study Status

Record Verification Date
June 2016
Overall Recruitment Status
Completed
Study Start Date
July 2012 (undefined)
Primary Completion Date
March 2013 (Actual)
Study Completion Date
April 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Juan J Badimon
Collaborators
AstraZeneca

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine whether treatment with ticagrelor (plus aspirin and bivalirudin) is more effective than treatment with clopidogrel (plus aspirin and bivalirudin).
Detailed Description
The HORIZONS-AMI Trial compared the effectiveness of heparin plus a glycoprotein IIb/IIIa inhibitor (GPI) versus bivalirudin in acute myocardial infarction (AMI) patients undergoing stent deployment 1. Overall the data showed benefits associated with the bivalirudin treatment with lower rates of all-cause mortality, cardiac mortality, re-infarction and non-CABG related major bleeding; However, the data seems to indicate a non-significant increase in acute stent thrombosis in the bivalirudin group. This observation seems to suggest the potential benefits of adding an antiplatelet agent to bivalirudin. A study by Dangas G et al found that in the HORIZONS-AMI patients, the group receiving 600 mg loading-dose of clopidogrel had significantly lower 30-day unadjusted rates of mortality, reinfarction and stent thrombosis than the 300 mg loading-dose group, without increase in bleeding rate. Furthermore, even though the benefits of bivalirudin were independent of the clopidogrel loading dose; the 600mg LD was associated with more benefits with both anticoagulation regimens. Similar observations have been reported in the ARMYDA-6 MI study. It is our hypothesis that using ticagrelor instead of clopidogrel, given its more potent and faster activity, would have greater antithrombotic activity and therefore may reduce the rate of acute stent thrombosis when administered in combination with bivalirudin + ASA in AMI patients. To investigate this hypothesis, we will compare the antithrombotic effects of ticagrelor with clopidogrel, when administered in combination with ASA and bivalirudin, in healthy human volunteers using a cross-over study design. The antithrombotic activity will be assessed pre-treatment and 2-hours and 24-hours post treatment, using methodologies including Badimon Perfusion chamber, VerifyNow P2Y12 assay, platelet aggregation with Multiplate Analyzer and Thromboelastography.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Coronary Syndrome
Keywords
Antiplatelet, ticagrelor, clopidogrel, bivalirudin, thrombosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
15 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Ticagrelor + ASA + Bivalirudin
Arm Type
Experimental
Arm Description
Single loading dose of Ticagrelor (180 mg given as two 90 mg tablets), plus single dose of ASA (one 81 mg tablet) + bivalirudin administered as 0.75 mg/kg IV bolus followed by 1.75 mg/kg/hour for 1 hour.
Arm Title
Clopidogrel + ASA + Bivalirudin
Arm Type
Active Comparator
Arm Description
Single loading dose of Clopidogrel (600 mg given as two 300 mg tablets), plus single dose of ASA (one 81 mg tablet) + bivalirudin administered as 0.75 mg/kg IV bolus followed by 1.75 mg/kg/hour for 1 hour.
Intervention Type
Drug
Intervention Name(s)
Ticagrelor + ASA + Bivalirudin
Other Intervention Name(s)
Brilinta (ticagrelor, Aspirin (ASA), Angiomax (bivalirudin)
Intervention Description
Single loading dose of Ticagrelor (180 mg given as two 90 mg tablets), plus single dose of ASA (one 81 mg tablet) + bivalirudin administered as 0.75 mg/kg IV bolus followed by 1.75 mg/kg/hour for 1 hour.
Intervention Type
Drug
Intervention Name(s)
Clopidogrel + ASA + Bivalirudin
Other Intervention Name(s)
Plavix (clopidogrel), Aspirin (ASA), Angiomax (bivalirudin)
Intervention Description
Single loading dose of Clopidogrel (600 mg given as two 300 mg tablets), plus single dose of ASA (one 81 mg tablet) + bivalirudin administered as 0.75 mg/kg IV bolus followed by 1.75 mg/kg/hour for 1 hour.
Primary Outcome Measure Information:
Title
Platelet-thrombus Formation in an ex Vivo Model of Thrombosis
Description
Change in thrombus size at 1 hour as compared to Pre-treatment baseline, where a positive change represents a decrease in thrombus size.
Time Frame
Pre-treatment baseline and 1 hour
Title
Platelet-thrombus Formation in an ex Vivo Model of Thrombosis
Description
Change in thrombus size at 24 hours as compared to Pre-treatment baseline, where a positive change represents a decrease in thrombus size.
Time Frame
Pre-treatment baseline and 24 hrs post treatment
Secondary Outcome Measure Information:
Title
Platelet Reactivity
Description
Platelet reactivity measured by VerifyNowP2Y12 assay measuring percent inhibition
Time Frame
Pre-treatment baseline
Title
Platelet Reactivity
Description
Platelet reactivity measured by VerifyNowP2Y12 assay measuring percent inhibition
Time Frame
1 hr post-treatment
Title
Platelet Reactivity
Description
Platelet reactivity measured by VerifyNowP2Y12 assay measuring percent inhibition
Time Frame
24-hours post-treatment
Title
Blood Thrombogenicity
Description
Coagulation times, assessed using the ROTEM thromboelastometry
Time Frame
Pre-treatment baseline
Title
Blood Thrombogenicity
Description
Coagulation times, assessed using the ROTEM thromboelastometry
Time Frame
1 hr post-treatment
Title
Blood Thrombogenicity
Description
Coagulation times, assessed using the ROTEM thromboelastometry
Time Frame
24-hours post-treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Male or female volunteers between 18 and 65 years old. Body mass index (BMI) 18 - 30 kg/m2 inclusive. Healthy as assessed by a detailed medical history and physical examination. Laboratory est results within the normal range. Ability to provide signed informed consent. Exclusion Criteria: History of clinically relevant disease, bleeding, acute infectious disease or signs of acute illness. Allergy or hypersensitivity to aspirin or thienopyridines, or atopy diagnosed by a physician. Use of medication within one month prior to study drug administration. History of drug abuse or alcohol consumption >20 g/day. Inability to abstain from intensive muscular effort or sport competition. Loss of >400 mL blood or blood donation within 3 months. Positive serology for hepatitis B (HBs Ag) or hepatitis C. Conditions associated with hemorrhagic risk. Positive pregnancy test.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Juan J Badimon, PhD
Organizational Affiliation
Icahn School of Medicine at Mount Sinai
Official's Role
Principal Investigator
Facility Information:
Facility Name
Icahn School of Medicine at Mount Sinai
City
New York
State/Province
New York
ZIP/Postal Code
10029
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
25104302
Citation
Zafar MU, Vorchheimer DA, Tewar MP, Giannarelli C, Crippa M, Sartori S, Rodriguez D, Baber U, Mehran R, Badimon JJ. Ticagrelor reduces thrombus formation more than clopidogrel, even when co-administered with bivalirudin. Thromb Haemost. 2014 Nov;112(5):1069-70. doi: 10.1160/TH14-03-0269. Epub 2014 Aug 7. No abstract available.
Results Reference
result

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Antithrombotic Effects of Ticagrelor Versus Clopidogrel

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