Study Effect of VIA-2291 on Atherosclerotic Vascular Inflammation in Patients Undergoing Elective Carotid Endarterectomy

• Status: Completed
• Trial end date: 2008-07-01
• Target enrollment: 0
• Participant gender: All

Summary

This is a study to compare the effect of VIA-2291 vs. Placebo on various inflammatory biomarkers in patients with carotid stenosis scheduled for elective carotid endarterectomy

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Tallikut Pharmaceuticals, Inc.
• Treatments: Atreleuton; Hydroxyurea; Lipoxygenase Inhibitors

Criteria

Inclusion Criteria:

• Female patients must be of non-childbearing potential

• Carotid stenosis between 60% and 90% and to be scheduled for CEA surgery

• One or more of the following clinical features: Prior history >4 weeks of cerebrovascular accident (CVA) or transient ischemic attack (TIA) consistent with North American Symptomatic Carotid Endarterectomy Trial (NASCET) criteria or prior history of amaurosis fugax occurring at any time

• Diabetes haemoglobin (Hb) A1c between 7.0 and 11% or a history of two or more fasting blood glucose levels >6.9 mmol/L

• Baseline hsCRP >2 mg/L

• Echolucent plaque

Exclusion Criteria:

• Acute CVA or TIA within 4 weeks of enrollment or the presence of ulcerated or unstable plaque requiring urgent carotid endarterectomy

• Renal insufficiency defined as creatinine >1.5 x upper limit of normal (ULN)

• Cirrhosis, recent hepatitis, alanine aminotransferase (ALT) >1 x ULN (i.e., above the normal range) or positive screening test for hepatitis B (hepatitis B surface antigen) or hepatitis C (by ELISA)

• Uncontrolled diabetes mellitus within 1 month prior to study screening, defined as HbA1c >11% at screening

• Congestive heart failure (CHF) defined by the New York Heart Association as functional Class III or IV

• Recent acute coronary syndrome event or coronary artery bypass graft (CABG) surgery (within 4 weeks of enrollment)

• Current atrial fibrillation

• Planned cardiac intervention

• Acetaminophen use in any form in the 7 days before enrollment