Phase
Condition
Congestive Heart Failure
Chest Pain
Heart Failure
Treatment
rhNRG-1 Dose 2
rhNRG-1 Dose 1
Placebo
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Age > 18 years.
Male or female subjects.
Have chronic heart failure defined as NYHA classification of II or III.
Be on a stable regimen of ACEI/ARB and/or beta-blocker 3 months prior to receivingstudy medication and are expected to remain on a stable HF medication regimethroughout the duration of the trial.
Left ventricular ejection fraction (LVEF) of < 35% as determined at screening by 2-Dechocardiography.
Is able to understand and provide informed consent.
If subject has dilated cardiomyopathy, ischemic heart disease or corrected valvularheart disease, and had surgery to repair or replace value, the surgery must havebeen performed 3 months prior to receiving study medication and the surgical area isfunctioning normally.
Proper birth control must be used at least 3 weeks prior to the study (women only),during the infusion period of study drug (men and women), 4-weeks after study drugadministration (men and women) and the remaining 11 months in the study follow-up (women). Women must have a negative pregnancy test at screening.
No greater than mild pericardial effusion < 0.5 cm on echocardiography (roughlycorresponds to < 100 mL).
Have an implantable cardioverter-defibrillator (ICD). The ICD should have beenimplanted at least 3 months prior to receiving study medication. Patients shouldundergo interrogation of their ICDs between 1 and 7 days before randomization todrug for the previous thirty (30) days. This interrogation would includesurveillance for ventricular arrhythmias as well as assessment of ICD discharge(s)and/or anti-tachycardia pacing.
Exclusion
Exclusion Criteria:
Has chronic heart failure classified as NYHA Class I or IV.
Has a history of any malignancy or positive test as specified in the pre-cancerscreening.
Have other conditions which in the opinion of the investigator precludeparticipation in the study, e.g. serious co-morbidity, known or suspected substanceabuse or non-compliance.
Has a body weight >350lbs.
Has had any cause hospitalization 30 days prior to screening.
Study Design
Study Description
Connect with a study center
University of California, San Diego
La Jolla, California 92037
United StatesSite Not Available
Metabolic Clinic and Research Center
Los Angeles, California 90033
United StatesSite Not Available
USC Cardiovascular Division
Los Angeles, California 90033
United StatesSite Not Available
Orange County Research Center
Tustin, California 92780
United StatesSite Not Available
University of Colorado Denver
Denver, Colorado 80045
United StatesSite Not Available
Clearwater Cardiovascular & Interventional Consultants, MD, PA
Clearwater, Florida 33756
United StatesSite Not Available
University of South Florida
Tampa, Florida 33606
United StatesSite Not Available
University of Iowa Hospitals and Clinics
Iowa City, Iowa 52242
United StatesSite Not Available
MedPharmics, LLC.
Kenner, Louisiana 70065
United StatesSite Not Available
Benchmark Research
Metairie, Louisiana 70006
United StatesSite Not Available
East Texas Cardiology
Houston, Texas 77002
United StatesSite Not Available
The Medical Center of Plano
Plano, Texas 75075
United StatesSite Not Available
Sentara Cardiovascular Research Institute
Norfolk, Virginia 23507
United StatesSite Not Available

Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.