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NCT03016325 · ClinicalTrials.gov registry record · Phase 2

Evaluate the Safety and Efficacy of 48-Hour Infusions of HNO (Nitroxyl) Donor in Hospitalized Patients With Heart Failure

A Phase 2 study, sponsored by Bristol-Myers Squibb.

Completed
Registry status
Phase 2
Development phase
329
Enrollment target

NCT03016325: Completed Phase 2 study, sponsored by Bristol-Myers Squibb.

NCT03016325 is a Phase 2 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 329 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (147% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03016325, a Phase 2 study, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 2
Development phase
329 participants
Enrollment target

Study Summary

A Study to Evaluate Safety and Efficacy of Continuous 48-Hour Intravenous Infusions of HNO Donor in Hospitalized Patients with Heart Failure and Impaired Systolic Function

Primary Outcome

Percentage of participants with clinically relevant hypotension, defined by systolic blood pressure (SBP) \< 90 mm Hg (confirmed by a repeated value \< 90 mm Hg) or symptoms of hypotension, up to 6 hours after the end of study drug infusion

Interventions

  • DRUG Placebo
  • DRUG HNO Donor

Trial Details

FieldValue
Enrollment Target 329 participants
Start Date 2017-01-13
Est. Completion 2019-11-12
Phase Phase 2
Bristol-Myers Squibb

1,025 total trials

What the finished NCT03016325 record still lists

NCT03016325 is an interventional study that assigns participants to a tested intervention. The registered 329 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (147% higher).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT03016325 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03016325 about?

NCT03016325 is a clinical study titled "Evaluate the Safety and Efficacy of 48-Hour Infusions of HNO (Nitroxyl) Donor in Hospitalized Patients With Heart Failure". A Study to Evaluate Safety and Efficacy of Continuous 48-Hour Intravenous Infusions of HNO Donor in Hospitalized Patients with Heart Failure and Impaired Systolic Function

What is the current status of trial NCT03016325?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 329 participants. The study started on 2017-01-13. Estimated completion is 2019-11-12.

What interventions are being tested in trial NCT03016325?

The interventions under investigation include: Placebo (DRUG), HNO Donor (DRUG).

Who is sponsoring clinical trial NCT03016325?

This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03016325's enrollment target sits among peer trials

329 146th of 2000 higher than 1,855 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03016325, the US trial registry maintained by the National Library of Medicine. NCT03016325 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.