Study to Evaluate the Safety of a Single Escalating Dose of ACRX-100 in Adults With Ischemic Heart Failure

PHASE1CompletedINTERVENTIONAL
Enrollment

17

Participants

Timeline

Start Date

February 28, 2010

Primary Completion Date

January 31, 2012

Study Completion Date

January 31, 2012

Conditions
Heart Failure
Interventions
BIOLOGICAL

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.

Trial Locations (4)

10032

Columbia University Medical Center, New York

35211

Cardiology, PC, Birmingham

60611

Northwestern University, Chicago

60612

Rush University Medical Center, Chicago

Sponsors
All Listed Sponsors
lead

Juventas Therapeutics, Inc.

INDUSTRY