Efficacy and Safety of Human Neuregulin-1 to Treat Stable Chronic Heart Failure

Last updated: February 6, 2025
Sponsor: Zensun Sci. & Tech. Co., Ltd.
Overall Status: Completed

Phase

2

Condition

Congestive Heart Failure

Chest Pain

Heart Failure

Treatment

rhNRG-1 Dose 2

rhNRG-1 Dose 1

Placebo

Clinical Study ID

NCT01251406
ZS-01-210
  • Ages > 18
  • All Genders

Study Summary

The mortality of chronic heart failure patients remains high. Recombinant human Neuregulin-1 (rhNRG-1, also called Neucardin) is a 61 amino acid peptide that acts directly on damaged heart muscle cells to restore their structure and function. This study will investigate the safety and efficacy of rhNRG-1 to treat stable chronic heart failure.

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

Total Participants: 67
Treatment Group(s): 3
Primary Treatment: rhNRG-1 Dose 2
Phase: 2
Study Start date:
January 01, 2012
Estimated Completion Date:
March 31, 2014

Study Description

This randomized, parallel, placebo-controlled, double-blind, multi-center study will assess the safety and efficacy of rhNRG-1 also known as Neucardin as a treatment for stable chronic heart failure.

A total of 120 subjects, who have chronic heart failure with a NYHA classification of II or III, and are on a stable regimen of ACEI/angiotensin receptor blocker (ARB), beta-blocker, and/or diuretic for at least 3 months prior to receiving study medication and anticipated to remain on the stable regimen through the treatment period can enroll as per specific inclusion and exclusion criteria.

Subjects will be hospitalized for 10 days during the treatment period and will be infused subcutaneously with rhNRG-1 or placebo.

Connect with a study center

  • University of California, San Diego

    La Jolla, California 92037
    United States

    Site Not Available

  • Metabolic Clinic and Research Center

    Los Angeles, California 90033
    United States

    Site Not Available

  • USC Cardiovascular Division

    Los Angeles, California 90033
    United States

    Site Not Available

  • Orange County Research Center

    Tustin, California 92780
    United States

    Site Not Available

  • University of Colorado Denver

    Denver, Colorado 80045
    United States

    Site Not Available

  • Clearwater Cardiovascular & Interventional Consultants, MD, PA

    Clearwater, Florida 33756
    United States

    Site Not Available

  • University of South Florida

    Tampa, Florida 33606
    United States

    Site Not Available

  • University of Iowa Hospitals and Clinics

    Iowa City, Iowa 52242
    United States

    Site Not Available

  • MedPharmics, LLC.

    Kenner, Louisiana 70065
    United States

    Site Not Available

  • Benchmark Research

    Metairie, Louisiana 70006
    United States

    Site Not Available

  • East Texas Cardiology

    Houston, Texas 77002
    United States

    Site Not Available

  • The Medical Center of Plano

    Plano, Texas 75075
    United States

    Site Not Available

  • Sentara Cardiovascular Research Institute

    Norfolk, Virginia 23507
    United States

    Site Not Available

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