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NCT02239146 · ClinicalTrials.gov registry record · Phase 1

Safety of rFXIII in Patients Following First Time Myocardial Revascularization Requiring Cardiopulmonary Bypass

A Phase 1 study, sponsored by Novo Nordisk A/S.

Completed
Registry status
Phase 1
Development phase
43
Enrollment target

NCT02239146: Completed Phase 1 study, sponsored by Novo Nordisk A/S.

NCT02239146 is a Phase 1 study that has completed, run by Novo Nordisk A/S. The registered enrollment target is 43 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (28% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02239146, a Phase 1 study, has completed, sponsored by Novo Nordisk A/S.

COMPLETED
Registry status
Phase 1
Development phase
43 participants
Enrollment target

Study Summary

This trial is conducted in Europe and the United States of America (USA). The aim of this trial is to evaluate the safety of escalating single doses of rFXIII (recombinant factor XIII, catridecacog) administered following first time myocardial revascularization requiring cardiopulmonary bypass (CPB).

Interventions

  • DRUG placebo
  • DRUG catridecacog

Trial Details

FieldValue
Enrollment Target 43 participants
Start Date 2005-10
Est. Completion 2008-01
Phase Phase 1
Novo Nordisk A/S

431 total trials

What the finished NCT02239146 record still lists

NCT02239146 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 43 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (28% lower).

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

NCT02239146 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02239146 about?

NCT02239146 is a clinical study titled "Safety of rFXIII in Patients Following First Time Myocardial Revascularization Requiring Cardiopulmonary Bypass". This trial is conducted in Europe and the United States of America (USA). The aim of this trial is to evaluate the safety of escalating single doses of rFXIII (recombinant factor XIII, catridecacog) administered following first time myocardial revascularization requiring cardiopulmonary bypass (CPB)...

What is the current status of trial NCT02239146?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 43 participants. The study started on 2005-10. Estimated completion is 2008-01.

What interventions are being tested in trial NCT02239146?

The interventions under investigation include: placebo (DRUG), catridecacog (DRUG).

Who is sponsoring clinical trial NCT02239146?

This trial is sponsored by Novo Nordisk A/S, which has 431 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02239146's enrollment target sits among peer trials

43 1100th of 2000 higher than 896 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 NCT02239146, the US trial registry maintained by the National Library of Medicine. NCT02239146 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.