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COMPLETED Phase 2

A Study of Continuous Infusions of HNO (Nitroxyl) Donor in Patients With Heart Failure and Impaired Systolic Function

NCT03357731 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to evaluate the effects of BMS-986231 on systolic and diastolic parameters in patients with heart failure and low ejection fraction.

Interventions

  • OTHER Placebo
  • DRUG HNO Donor
  • DRUG Nitroglycerin (NTG)

Study Locations (18)

Other

  • Local Institution — Groiningen
  • Local Institution — Edinburgh
  • Local Institution — Glasgow
  • Local Institution — Glasgow
  • Local Institution — Glasgow
  • Local Institution — Harrow
  • Local Institution — London
  • Local Institution — London
  • Local Institution — London

California

  • Orange County Research Center — Tustin

Illinois

  • Northwestern Medicine — Chicago

Indiana

  • Indiana University School of Medicine-Indianapolis — Indianapolis

Massachusetts

  • Brigham and Womens Hospital — Boston

North Carolina

  • Duke Advanced Heart and Lung Failure Clinic — Durham

Virginia

  • Inova Heart and Vascular Institute — Falls Church

Aichi-ken

  • Local Institution — Nagoya

Trial Details

FieldValue
Enrollment Target 49 participants
Start Date 2017-11-30
Est. Completion 2019-05-10
Phase Phase 2

Sponsor

Bristol-Myers Squibb

504 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03357731

The ClinicalTrials.gov registry entry for NCT03357731 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 49 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Bristol-Myers Squibb, which has 504 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Heart Failure appearing as the primary indexed condition, and to 3 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03357731 reports 18 study locations spanning 10 distinct geographic areas — top geographies include Other, California, Illinois. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT03357731 about?

NCT03357731 is a clinical study titled "A Study of Continuous Infusions of HNO (Nitroxyl) Donor in Patients With Heart Failure and Impaired Systolic Function". The purpose of this study is to evaluate the effects of BMS-986231 on systolic and diastolic parameters in patients with heart failure and low ejection fraction.

What is the current status of trial NCT03357731?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 49 participants. The study started on 2017-11-30. Estimated completion is 2019-05-10.

What conditions does trial NCT03357731 study?

This clinical trial studies the following conditions: Heart Failure, Cardiac Failure, Reduced Ventricular Ejection Fraction. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03357731?

The interventions under investigation include: Placebo (OTHER), HNO Donor (DRUG), Nitroglycerin (NTG) (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03357731?

This trial is sponsored by Bristol-Myers Squibb, which has 504 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03357731 being conducted?

This trial has 18 study locations across California, Illinois, Indiana, Massachusetts, North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial