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Safety and Efficacy of Arformoterol Tartrate Inhalation Solution in Subjects With Chronic Obstructive Pulmonary Disease
NCT00250679 · View on ClinicalTrials.gov ↗
Study Summary
To evaluate the long-term safety and monitor the long-term efficacy of arformoterol over a period of 6 months in subjects with chronic obstructive pulmonary disease (COPD).
Conditions Studied
Interventions
- DRUG Placebo
- DRUG Arformoterol tartrate inhalation solution
- DRUG Arformoterol 25 ųg BID
- DRUG Formoterol 12 ųg BID
Study Locations (20)
California
- — Carmichael
- — Fullerton
- — Long Beach
- — Paramount
- — Rancho Mirage
- — San Diego
- — Walnut Creek
Florida
- — Bay Pines
- — Brandon
- — Gainesville
- — Panama City
- — Tampa
Alabama
- — Birmingham
- — Jasper
- — Mobile
Georgia
- — Atlanta
- — Marietta
Arkansas
- — Little Rock
Colorado
- — Denver
Connecticut
- — Hartford
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 443 participants |
| Start Date | 2005-10 |
| Est. Completion | 2007-10 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00250679
The ClinicalTrials.gov registry entry for NCT00250679 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 443 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Sumitomo Pharma America, which has 65 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 3 conditions, with Chronic Obstructive Pulmonary Disease appearing as the primary indexed condition, and to 4 interventions — of which Placebo 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: NCT00250679 reports 20 study locations spanning 7 distinct geographic areas — top geographies include California, Florida, 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 NCT00250679 about?
NCT00250679 is a clinical study titled "Safety and Efficacy of Arformoterol Tartrate Inhalation Solution in Subjects With Chronic Obstructive Pulmonary Disease". To evaluate the long-term safety and monitor the long-term efficacy of arformoterol over a period of 6 months in subjects with chronic obstructive pulmonary disease (COPD).
What is the current status of trial NCT00250679?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 443 participants. The study started on 2005-10. Estimated completion is 2007-10.
What conditions does trial NCT00250679 study?
This clinical trial studies the following conditions: Chronic Obstructive Pulmonary Disease, Emphysema, Bronchitis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00250679?
The interventions under investigation include: Placebo (DRUG), Arformoterol tartrate inhalation solution (DRUG), Arformoterol 25 ųg BID (DRUG), Formoterol 12 ųg BID (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00250679?
This trial is sponsored by Sumitomo Pharma America, which has 65 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00250679 being conducted?
This trial has 20 study locations across Alabama, Arkansas, California, Colorado, Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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