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Confirmatory Dose Finding Study of 2 Dosages of CHF 4226 pMDI (Carmoterol) in Patients With COPD
NCT00640484 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to confirm the dose of CHF 4226 (carmoterol) that should be given once a day to patients with COPD in order for the effect to last for 24 hours.
Conditions Studied
Interventions
- DRUG placebo
- DRUG carmoterol (CHF 4226)
- DRUG salmeterol
Study Locations (15)
Arizona
- Horizon Clinical Research Associates, PLLC — Gilbert
- Pulmonary Associates, PA — Phoenix
Oregon
- Clinical Research Institute of Southern Oregon, PC — Medford
- Asthma Allergy Associates — Portland
California
- UCLA David Geffen School of Medicine — Los Angeles
Florida
- University Clinical Research - DeLand, LLC — DeLand
Georgia
- Pulmonary Medicine and Critical Care — Austell
Illinois
- Sneeze, Wheeze & Itch Associates, LLC — Normal
Kentucky
- Commonwealth BioMedical Research — Madisonville
North Carolina
- North Carolina Clinical Research — Raleigh
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 57 participants |
| Start Date | 2008-04 |
| Est. Completion | 2008-10 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00640484
The ClinicalTrials.gov registry entry for NCT00640484 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 57 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Chiesi Farmaceutici S.p.A., which has 7 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 Chronic Obstructive Pulmonary Disease appearing as the primary indexed condition, and to 3 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: NCT00640484 reports 15 study locations spanning 13 distinct geographic areas — top geographies include Arizona, Oregon, California. 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 NCT00640484 about?
NCT00640484 is a clinical study titled "Confirmatory Dose Finding Study of 2 Dosages of CHF 4226 pMDI (Carmoterol) in Patients With COPD". The purpose of this study is to confirm the dose of CHF 4226 (carmoterol) that should be given once a day to patients with COPD in order for the effect to last for 24 hours.
What is the current status of trial NCT00640484?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 57 participants. The study started on 2008-04. Estimated completion is 2008-10.
What conditions does trial NCT00640484 study?
This clinical trial studies the following conditions: Chronic Obstructive Pulmonary Disease. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00640484?
The interventions under investigation include: placebo (DRUG), carmoterol (CHF 4226) (DRUG), salmeterol (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00640484?
This trial is sponsored by Chiesi Farmaceutici S.p.A., which has 7 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00640484 being conducted?
This trial has 15 study locations across Arizona, California, Florida, Georgia, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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