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NCT01092325 · ClinicalTrials.gov registry record · Phase 1

Safety and Hemodynamic Effects and Pharmacokinetics of CXL-1020 in Patients With Stable Heart Failure

A Phase 1 study, sponsored by Bristol-Myers Squibb.

Completed
Registry status
Phase 1
Development phase
28
Enrollment target

NCT01092325: Completed Phase 1 study, sponsored by Bristol-Myers Squibb.

NCT01092325 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 28 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (53% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01092325, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 1
Development phase
28 participants
Enrollment target

Study Summary

A Phase 1-2a Study of CXL-1020-01 in Patients with Stable Heart Failure

Primary Outcome

Safety is measured by assessment of multiple parameters including standard laboratory safety, changes in blood pressure and heart rate, changes in electrocardiogram, monitoring of heart rhythm via holter monitor, measurement of cardiac safety biomarkers such as plasma troponin as well as treatment emergent adverse events

Interventions

  • DRUG CXL-1020
  • DRUG Placebo for CXL-1020 Cohort 1
  • DRUG Placebo for CXL-1020 Cohort 2
  • DRUG CXL-1020 Dose for Echo Cohort A

Trial Details

FieldValue
Enrollment Target 28 participants
Start Date 2009-06
Est. Completion 2010-05
Phase Phase 1
Bristol-Myers Squibb

1,025 total trials

What the finished NCT01092325 record still lists

NCT01092325 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 28 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (53% lower).

The record links to 0 conditions, and to 4 interventions - of which CXL-1020 is the first listed.

NCT01092325 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01092325 about?

NCT01092325 is a clinical study titled "Safety and Hemodynamic Effects and Pharmacokinetics of CXL-1020 in Patients With Stable Heart Failure". A Phase 1-2a Study of CXL-1020-01 in Patients with Stable Heart Failure

What is the current status of trial NCT01092325?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 28 participants. The study started on 2009-06. Estimated completion is 2010-05.

What interventions are being tested in trial NCT01092325?

The interventions under investigation include: CXL-1020 (DRUG), Placebo for CXL-1020 Cohort 1 (DRUG), Placebo for CXL-1020 Cohort 2 (DRUG), CXL-1020 Dose for Echo Cohort A (DRUG).

Who is sponsoring clinical trial NCT01092325?

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 NCT01092325's enrollment target sits among peer trials

28 1447th of 2000 higher than 538 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT01092325, the US trial registry maintained by the National Library of Medicine. NCT01092325 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.