Study identifier:D5130L00013
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
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
Stable coronary artery disease
Phase 4
No
Ticagrelor, Clopidogrel
All
50
Interventional
18 Years - 150 Years
Allocation: Randomized
Endpoint Classification: Pharmacodynamics Study
Intervention Model: Crossover Assignment
Masking: Open Label
Primary Purpose: Treatment
Verified 01 Sept 2014 by AstraZeneca
AstraZeneca
-
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
Location
Location
Washington, DC, United States
Location
Towson, MD, United States
Location
Newark, DE, United States
Location
Beaumont, TX, United States
Location
Jacksonville, FL, United States
Location
Atlanta, GA, United States
Location
Wilmington, DE, United States
Location
Hollywood, FL, United States
Arms | Assigned Interventions |
---|---|
Experimental: Ticagrelor | Drug: Ticagrelor Min - 90mg/Max - 180mg tablets (loading dose) |
Active Comparator: Clopidogrel | Drug: Clopidogrel 75mg (once daily)/Max - 600mg tablets (loading dose) |
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