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COMPLETED Phase 3

A Trial to Evaluate the Efficacy and Safety of Formoterol Fumarate in the Treatment of Patients With COPD

NCT00215436 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to determine the safety and efficacy of the investigational drug in comparison with a placebo.

Conditions Studied

Interventions

  • DRUG Formoterol Fumarate

Study Locations (20)

California

  • Research Site — Buena Park
  • Research Site — Huntington Beach
  • Research Site — Long Beach
  • Research Site — Long Beach
  • Research Site — Los Angeles
  • Research Site — San Diego
  • Research Site — Stockton

Florida

  • Research Site — Clearwater
  • Research Site — DeLand
  • Research Site — Tampa

Arizona

  • Research Site — Phoenix
  • Research Site — Tuscon

Colorado

  • Research Site — Denver
  • Research Site — Wheat Ridge

Illinois

  • Research Site — Hines
  • Research Site — Normal

Alabama

  • Research Site — Jasper

Connecticut

  • Research Site — Hartford

Georgia

  • Research Site — Woodstock

Trial Details

FieldValue
Enrollment Target 345 participants
Start Date 2005-03
Est. Completion 2006-09
Phase Phase 3

Sponsor

Dey

6 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00215436

The ClinicalTrials.gov registry entry for NCT00215436 describes a study currently listed as completed. It is categorized as Phase 3, 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 345 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Dey, which has 6 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 COPD appearing as the primary indexed condition, and to 1 intervention — of which Formoterol Fumarate 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: NCT00215436 reports 20 study locations spanning 9 distinct geographic areas — top geographies include California, Florida, Arizona. 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 NCT00215436 about?

NCT00215436 is a clinical study titled "A Trial to Evaluate the Efficacy and Safety of Formoterol Fumarate in the Treatment of Patients With COPD". The purpose of this study is to determine the safety and efficacy of the investigational drug in comparison with a placebo.

What is the current status of trial NCT00215436?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 345 participants. The study started on 2005-03. Estimated completion is 2006-09.

What conditions does trial NCT00215436 study?

This clinical trial studies the following conditions: COPD. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00215436?

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

Who is sponsoring clinical trial NCT00215436?

This trial is sponsored by Dey, which has 6 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00215436 being conducted?

This trial has 20 study locations across Alabama, Arizona, California, Colorado, Connecticut. 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