Pharmacogenetic Study of Warfarin Dose-Response: a Prospective Trial (PGxWarfarin)
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|ClinicalTrials.gov Identifier: NCT00654823|
Recruitment Status : Unknown
Verified April 2008 by Sheba Medical Center.
Recruitment status was: Not yet recruiting
First Posted : April 9, 2008
Last Update Posted : April 9, 2008
We propose to develop a personalized pharmacogenetic approach including the major genetic markers of warfarin (coumadin) dosing and patients' age and weight. The known genetic determinants include several functional and common polymorphisms in CYP2C9 and VKORC1 genes, which explain the low-end of warfarin dosing range and mostly occur in patients of Caucasian and Chinese origins. We identified a new VKORC1 polymorphism that is specifically indicative of the high dose requirements and is dominant over the dose-reducing effect of the known CYP2C9 and VKORC1 markers. This marker is significantly over-represented in Jews of Ethiopian origin, but is also common in Ashkenazis, it is also linked to the VKORC1 genetic markers characteristic of the Afro-American population (published in Blood 2007, 109:2477-80). This information prompts the development of a more inclusive and universal diagnostic approach to the individualized warfarin therapy.
The present study aims at evaluation of our novel pharmacogenetic model for predicting warfarin (coumadin) dose response on the basis of patient's genetic markers of warfarin sensitivity and resistance, and other patient specific factors. To this end, we proposes to re-evaluate our previously developed pharmacogenetic model in stabilized warfarin treated patients (N=200) and then to implement it in a prospective study of patients new on warfarin as compared to the "traditionally" treated patients (N=500).
|Condition or disease|
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|Study Type :||Observational|
|Estimated Enrollment :||500 participants|
|Official Title:||Prospective Study Comparing Between the Commonly-Used and Pharmacogenetically-Guided Warfarin Administration Protocols|
|Study Start Date :||June 2008|
|Estimated Primary Completion Date :||June 2010|
|Estimated Study Completion Date :||June 2011|
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00654823
|Institute of Clinical Pharmacology||Not yet recruiting|
|Tel Hashomer, Israel, 52621|
|Contact: Eva Gak, PhD 972-3-530-3946 firstname.lastname@example.org|
|Principal Investigator: Ronen Loebstein, MD|
|Principal Investigator:||Ronen Loebstein, MD||Sheba Medical Center|