This is a dose ranging study to compare the effect of VIA-2291 vs. Placebo on various inflammatory biomarkers in patients with recent acute coronary events
This is a Phase II, randomized, double-blind, placebo-controlled study of the effect of VIA-2291 on atherosclerotic vascular inflammation
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
191
MIMA Century Research Associates
Melbourne, Florida, United States
Minneapolis Heart Institute
Minneapolis, Minnesota, United States
Cardiology Associates Research, LLC
Tupelo, Mississippi, United States
Change From Baseline on ex Vivo Leukotriene B4 Synthesis in Whole Blood
Time frame: Baseline and 12 weeks
Change From Baseline in Leukotriene E4 (LTE4)
Urinary LTE4 is expressed in pg per mg Creatinine (pg/mg Cr) to normalize for renal excretion rate
Time frame: Baseline and 12 weeks
Change From Baseline in High Sensitivity C-reactive Protein (hsCRP) - Core Study
Time frame: Baseline and 12 weeks
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LeBauer Cardiovascular Research Foundation
Greensboro, North Carolina, United States
Victoria Heart and Vascular Center
Victoria, Texas, United States
Foothills Medical Center
Calgary, Alberta, Canada
Victoria Heart Institute Foundation
Victoria, British Columbia, Canada
Queen Elizabeth II HSC
Halifax, Nova Scotia, Canada
Montreal Heart Institute
Montreal, Quebec, Canada
Notre Dame Hospital
Montreal, Quebec, Canada
...and 2 more locations