17
Participants
Start Date
February 28, 2010
Primary Completion Date
January 31, 2012
Study Completion Date
January 31, 2012
ACRX-100
Three cohorts (16 total subjects) will be studied. There will be no concurrent controls. The dose will be escalated by increasing the total amount of ACRX-100 delivered per subject from low dose (n=4 subjects) to middle dose (n=6 subjects) to high dose (n=6 subjects). ACRX-100 will be injected directly into the myocardium as a single dose at multiple sites through a percutaneous, left ventricular approach using a needle injection catheter.
Columbia University Medical Center, New York
Cardiology, PC, Birmingham
Northwestern University, Chicago
Rush University Medical Center, Chicago
Lead Sponsor
Juventas Therapeutics, Inc.
INDUSTRY