A Pharmacodynamic Study With Ticagrelor in Hispanic 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: | April 2012 |
End Date: | October 2013 |
Contact: | AstraZeneca Clinical Study Information |
Email: | information.center@astrazeneca.com |
Phone: | 800-236-9933 |
A Randomized, Open-Label, Multiple Dose, Crossover, Multiple Center Study of the Antiplatelet Effects of Ticagrelor Versus Clopidogrel in Hispanic Patients With Stable Coronary Artery Disease
The purpose of this study is to assess the pharmacodynamic effect of ticagrelor in Hispanic
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 Hispanic 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 Hispanic
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 requiring dialysis
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