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Principal Investigator:
Safwan Kassas, MD
(Covenant)
Alok Maheshwari, MD (St. Marys)
Daniel Lee, MD (Bay Med)
William Felten, MD (Midland)
Sub-Investigators:
William Felten,
MD Gregory Pellizzon,
MD
Kondaramvalappil Ravindran, MD Umesh Badami, MD
Manoj Sharma, MD
Peter Fattal, MD
Susan Sallach, MD John
Collins, MD
Shiraz Shariff, MD Rao
Gudipati, MD
Stephen Mattichak, MD Nilofar Islam,
MD
Rami Safadi, MD Tanveer
Malik MD
Robert Genovese MD Edwin Flattery, PA-C
Sponsor:
Schering-Plough Research Institute,
a Division of Schering Corporation
Study
Purpose:
A Multicenter, Randomized, Double-Blind,
Placebo-Controlled Study to Evaluate the Safety and Efficacy of SCH 530348 in
Addition to Standard of Care in Subjects With Acute Coronary Syndrome: Thrombin
Receptor Antagonist for Clinical Event Reduction
in Acute Coronary Syndrome (TRA•CER)
Objective:
To evaluate the hypothesis that SCH
530348 added to standard of care will reduce the incidence of atherothrombotic
ischemic events relative to standard of care alone, as measured by the composite
of cardiovascular death, myocardial infarction (MI), stroke, recurrent ischemia
with rehospitalization, and urgent coronary revascularization.
Status:
Active enrollment
If you have any
questions, please feel free to contact the coordinators, and they will be happy
to answer any questions you have regarding this study.
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