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NCT01065077 · ClinicalTrials.gov registry record · Phase 2

BAY58-2667 Dose Finding Trial Investigating Fixed Doses in Patients With Acute Decompensated Chronic Congestive Heart Failure (ADHF)

A Phase 2 study, sponsored by Bayer.

Terminated
Registry status
Phase 2
Development phase
12
Enrollment target

NCT01065077: Clinical Trial Phase 2 study, sponsored by Bayer.

NCT01065077 is a Phase 2 study that was terminated before completion, run by Bayer. The registered enrollment target is 12 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (91% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01065077, a Phase 2 study, was terminated before completion, sponsored by Bayer.

TERMINATED
Registry status
Phase 2
Development phase
12 participants
Enrollment target

Study Summary

A placebo controlled, double-blind and randomized study to assess different doses of a new drug (BAY58-2667) given intravenously, to evaluate if it is safe and can help to improve the well-being of patients with acute decompensated heart failure.

Interventions

  • DRUG Placebo
  • DRUG Cinaciguat (BAY58-2667)

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2010-03
Est. Completion 2011-02
Phase Phase 2
Bayer

591 total trials

Why NCT01065077 stopped before completion

NCT01065077 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (91% lower).

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

NCT01065077 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01065077 about?

NCT01065077 is a clinical study titled "BAY58-2667 Dose Finding Trial Investigating Fixed Doses in Patients With Acute Decompensated Chronic Congestive Heart Failure (ADHF)". A placebo controlled, double-blind and randomized study to assess different doses of a new drug (BAY58-2667) given intravenously, to evaluate if it is safe and can help to improve the well-being of patients with acute decompensated heart failure.

What is the current status of trial NCT01065077?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 12 participants. The study started on 2010-03. Estimated completion is 2011-02.

What interventions are being tested in trial NCT01065077?

The interventions under investigation include: Placebo (DRUG), Cinaciguat (BAY58-2667) (DRUG).

Who is sponsoring clinical trial NCT01065077?

This trial is sponsored by Bayer, which has 591 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01065077's enrollment target sits among peer trials

12 1948th of 2000 higher than 34 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 NCT01065077, the US trial registry maintained by the National Library of Medicine. NCT01065077 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.