« Previous
Next »
American Heart Journal
Volume 157, Issue 2
, Pages
369-374
, February 2009
Bleeding risk associated with 1 year of dual antiplatelet therapy after percutaneous coronary intervention: Insights from the Clopidogrel for the Reduction of Events During Observation (CREDO) trial
To access this article, please choose from the options below
The CREDO trial was funded by Bristol-Myers Squibb (New York, NY)/Sanofi-Synthelabo (Paris, France) partnership. The study sponsors played no role in the design of this substudy, nor in the collection, analysis, or interpretation of these data.
Dr. Aronow is on the Speakers' Bureau for and has received grant funding from Bristol-Myers Squibb-Sanofi. Ms. Brennan has no conflicts of interest to disclose. Drs Topol and Steinhubl received research grants from Sanofi-Aventis and Bristol-Myers Squibb to conduct the trial; Dr. Steinhubl served as a consultant to this company in the clinical development of clopidogrel. Dr Steinhubl is currently employed by the Medicines Company (Parsippany, NJ). Dr Berger has received honoraria for speaking at Bristol-Myers Squibb-Sanofi–sponsored symposia.
PII: S0002-8703(08)00805-3
doi: 10.1016/j.ahj.2008.09.011
© 2009 Mosby, Inc. All rights reserved.
« Previous
Next »
American Heart Journal
Volume 157, Issue 2
, Pages
369-374
, February 2009
