A Dose-Defining Study of CXL-1020 in Patients With Systolic Heart Failure

PHASE2CompletedINTERVENTIONAL
Enrollment

69

Participants

Timeline

Start Date

April 30, 2010

Primary Completion Date

February 29, 2012

Study Completion Date

February 29, 2012

Conditions
Heart Failure
Interventions
DRUG

Placebo

An infusion of an identically appearing solution of sugar water will be intravenously administered.

DRUG

Strata 1 CXL-1020

Intravenous infusion of CXL-1020, up-titrated, so that 3 different dosages are administered over 6 hours

DRUG

Strata 2 CXL-1020

One of 3 different dosages of CXL-1020 administered at a fixed dosage level for 6 hours.

DRUG

Strata 3 CXL-1020

A fixed dose level of CXL-1020 will be administered for the initial 6 hours of treatment in Strata 3 and then dosage will be altered up or downward based on the investigators observation of the patient's condition.

Trial Locations (15)

10467

Montefiore Medical Center, The Bronx

21201

University of Maryland Medical Center, Baltimore

27157

Wake Forest University Health Sciences, Winston-Salem

29425

Medical University of South Carolina, Charleston

32209

University of Florida, Jacksonville

32610

University of Florida, Gainesville

32804

Florida Hospital Transplant Center, Orlando

38138

Stern Cardiovascular Center PA, Germantown

43210

Davis Heart & Lung Research Institute, Columbus

44106

University Hospitals Case Medical Center, Cleveland

45267

University of Cincinnati, Cincinnati

48201

DMC Cardiovascular Institute, Detroit

48202

Henry Ford Health System, Detroit

70121

Ochsner Clinic Foundation, New Orleans

07103

University of Medicine & Dentistry of New Jersey - New Jersey Medical School, South Orange

Sponsors
All Listed Sponsors
collaborator

Cardioxyl Pharmaceuticals, Inc

INDUSTRY

lead

Bristol-Myers Squibb

INDUSTRY

NCT01096043 - A Dose-Defining Study of CXL-1020 in Patients With Systolic Heart Failure | Biotech Hunter | Biotech Hunter