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NCT00116012 · ClinicalTrials.gov registry record · Phase 2

Anticoagulation With rNAPc2 to Eliminate MACE/TIMI 32

A Phase 2 study, sponsored by ARCA Biopharma.

Completed
Registry status
Phase 2
Development phase
300
Enrollment target

NCT00116012: Completed Phase 2 study, sponsored by ARCA Biopharma.

NCT00116012 is a Phase 2 study that has completed, run by ARCA Biopharma. The registered enrollment target is 300 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (126% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00116012, a Phase 2 study, has completed, sponsored by ARCA Biopharma.

COMPLETED
Registry status
Phase 2
Development phase
300 participants
Enrollment target

Study Summary

The primary focus of this study is to explore the safety of a range of doses of rNAPc2 in subjects who are managed in hospitals that most typically practice an early invasive strategy (catheterization during the index admission). After completion of the ascending dose-ranging part of the trial and review of these data by the Data and Safety Monitoring Board (DSMB), the maximum tolerated dose of rNAPc2 will be studied in single-arm, open-label panels (approximately 25 subjects each) of rNAPc2 with descending doses of unfractionated heparin (UFH).

Interventions

  • DRUG rNAPc2

Trial Details

FieldValue
Enrollment Target 300 participants
Start Date 2005-06
Phase Phase 2
ARCA Biopharma

10 total trials

What the finished NCT00116012 record still lists

NCT00116012 is an interventional study that assigns participants to a tested intervention. The registered 300 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 (126% higher).

The record links to 0 conditions, and to 1 intervention - of which rNAPc2 is the first listed.

NCT00116012 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00116012 about?

NCT00116012 is a clinical study titled "Anticoagulation With rNAPc2 to Eliminate MACE/TIMI 32". The primary focus of this study is to explore the safety of a range of doses of rNAPc2 in subjects who are managed in hospitals that most typically practice an early invasive strategy (catheterization during the index admission). After completion of the ascending dose-ranging part of the trial and r...

What is the current status of trial NCT00116012?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 300 participants. The study started on 2005-06.

What interventions are being tested in trial NCT00116012?

The interventions under investigation include: rNAPc2 (DRUG).

Who is sponsoring clinical trial NCT00116012?

This trial is sponsored by ARCA Biopharma, which has 10 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00116012's enrollment target sits among peer trials

300 167th of 2000 higher than 1,813 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 NCT00116012, the US trial registry maintained by the National Library of Medicine. NCT00116012 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.