A Pharmacodynamic Study With Ticagrelor in African American Patients



Status:Completed
Conditions:Peripheral Vascular Disease, Cardiology
Therapuetic Areas:Cardiology / Vascular Diseases
Healthy:No
Age Range:18 - Any
Updated:7/16/2013
Start Date:March 2012
End Date:July 2013
Contact:AstraZeneca Clinical Study Information
Email:information.center@astrazeneca.com
Phone:800-236-9933

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A Randomized, Open-Label, Multiple Dose, Crossover, Multiple Center Study of the Antiplatelet Effects of Ticagrelor Versus Clopidogrel in African American Patients With Stable Coronary Artery Disease


The purpose of this study is to assess the pharmacodynamic effect of ticagrelor in African
American patients with stable coronary artery disease.


A Randomized, Open-Label, Multiple Dose, Crossover, Multiple Center Study of the
Antiplatelet Effects of Ticagrelor versus Clopidogrel in African American Patients with
Stable Coronary Artery Disease

Inclusion Criteria:

- Provision of signed and dated informed consent before initiation of any study-related
procedures

- Male or female patients aged 18 years or older

- Documented stable CAD fulfilling and taking 75-100mg ASA daily treatment

- Females must be post menopausal or surgically sterile Self-identified as African
American

Exclusion Criteria:

- Any indication for oral anticoagulant (e.g., atrial fibrillation, mitral stenosis or
prosthetic heart valve) or dual antiplatelet treatment (e.g., clopidogrel, prasugrel,
ASA dose other than 75 to 100 mg daily) during study period

- Patients who had ACS or stent placed within 12 months of screening Patients with a
history of moderate or severe hepatic impairment

- Current smokers, including the use of tobacco containing products in the past 1 month
of randomization Patients required dialysis
We found this trial at
6
sites
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Washington,
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Atlanta, GA
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Houston, TX
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Newark, DE
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