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NCT00677053 · ClinicalTrials.gov registry record · Phase 2
Safety and Efficacy of TAK-442 in Subjects With Acute Coronary Syndromes
A Phase 2 study of Acute Coronary Syndrome, sponsored by Takeda.
- Completed
- Registry status
- Phase 2
- Development phase
- 2,753
- Enrollment target
- 20
- Study locations
NCT00677053 is a Phase 2 study of Acute Coronary Syndrome that has completed, run by Takeda. The registered enrollment target is 2,753 participants, roughly in line with the 2,653-participant average among 40 other Acute Coronary Syndrome trials with a reported enrollment target. The trial reports 20 study locations across 15 states.
The verdict
NCT00677053, a Phase 2 study of Acute Coronary Syndrome, has completed, sponsored by Takeda.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 2,753 participants
- Enrollment target
- 20
- Study locations
Study Summary
The purpose of this study is to determine the safety and tolerability of multiple doses of TAK-442once daily, (QD) or twice daily (BID), in subjects with acute coronary syndrome (unstable angina, myocardial infarction).
Conditions Studied
Interventions
- DRUG TAK-442
Study Locations (20)
Other
- - Buenos Aires
- - Bonheiden
- - Genk
- - Liège
- - Porto Algere
Texas
- - Houston
- - Victoria
Alabama
- - Birmingham
Arizona
- - Tucson
Delaware
- - Newark
District of Columbia
- - Washington D.C.
Florida
- - Pensecola
Iowa
- - West Des Moines
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 2,753 participants |
| Start Date | 2008-03 |
| Est. Completion | 2010-06 |
| Phase | Phase 2 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00677053
The ClinicalTrials.gov registry entry for NCT00677053 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 2,753 participants, a figure that helps gauge the scale of data the investigators plan to collect, roughly in line with the 2,653-participant average among 40 other Acute Coronary Syndrome trials with a reported enrollment target. The listed sponsor is Takeda, which has 408 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Acute Coronary Syndrome appearing as the primary indexed condition, and to 1 intervention - of which TAK-442 is the first listed.
NCT00677053 reports 20 study locations spanning 15 distinct geographic areas - top geographies include Other, Texas, Alabama.
Frequently Asked Questions
What is clinical trial NCT00677053 about?
NCT00677053 is a clinical study titled "Safety and Efficacy of TAK-442 in Subjects With Acute Coronary Syndromes". The purpose of this study is to determine the safety and tolerability of multiple doses of TAK-442once daily, (QD) or twice daily (BID), in subjects with acute coronary syndrome (unstable angina, myocardial infarction).
What is the current status of trial NCT00677053?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 2,753 participants. The study started on 2008-03. Estimated completion is 2010-06.
What conditions does trial NCT00677053 study?
This clinical trial studies the following conditions: Acute Coronary Syndrome.
What interventions are being tested in trial NCT00677053?
The interventions under investigation include: TAK-442 (DRUG).
Who is sponsoring clinical trial NCT00677053?
This trial is sponsored by Takeda, which has 408 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00677053 being conducted?
This trial has 20 study locations across Alabama, Arizona, Delaware, District of Columbia, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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