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COMPLETED Phase 2

Safety and Efficacy of TAK-442 in Subjects With Acute Coronary Syndromes

NCT00677053 · View on ClinicalTrials.gov ↗

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

FieldValue
Enrollment Target 2,753 participants
Start Date 2008-03
Est. Completion 2010-06
Phase Phase 2

Sponsor

Takeda

387 total trials

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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. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 2,753 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Takeda, which has 387 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00677053 reports 20 study locations spanning 15 distinct geographic areas — top geographies include Other, Texas, Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00677053?

The interventions under investigation include: TAK-442 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00677053?

This trial is sponsored by Takeda, which has 387 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial