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NCT01067859 · ClinicalTrials.gov registry record · Phase 2
A Phase IIb Study to Investigate the Efficacy and Tolerability of Lower Doses Cinaciguat (25 µg/h, 10 µg/h) Given Intravenously to Patients With Acute Decompensated Chronic Congestive Heart Failure (ADHF)
A Phase 2 study, sponsored by Bayer.
- Terminated
- Registry status
- Phase 2
- Development phase
- 5
- Enrollment target
NCT01067859 is a Phase 2 study that was terminated before completion, run by Bayer. The registered enrollment target is 5 participants.
The verdict
NCT01067859, a Phase 2 study, was terminated before completion, sponsored by Bayer.
- TERMINATED
- Registry status
- Phase 2
- Development phase
- 5 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
| Field | Value |
|---|---|
| Enrollment Target | 5 participants |
| Start Date | 2010-03 |
| Est. Completion | 2010-11 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01067859
The ClinicalTrials.gov registry entry for NCT01067859 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 5 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Bayer, which has 591 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT01067859 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01067859 about?
NCT01067859 is a clinical study titled "A Phase IIb Study to Investigate the Efficacy and Tolerability of Lower Doses Cinaciguat (25 µg/h, 10 µg/h) Given Intravenously to 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 NCT01067859?
This trial is currently terminated. It is a Phase 2 study. The enrollment target is 5 participants. The study started on 2010-03. Estimated completion is 2010-11.
What interventions are being tested in trial NCT01067859?
The interventions under investigation include: Placebo (DRUG), Cinaciguat (BAY58-2667) (DRUG).
Who is sponsoring clinical trial NCT01067859?
This trial is sponsored by Bayer, which has 591 total clinical trials registered on ClinicalTrials.gov.
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