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A Study To Investigate The Safety, Toleration And Efficacy of PF00610355 In Chronic Obstructive Pulmonary Disease (COPD) Patients.
NCT00808288 · View on ClinicalTrials.gov ↗
Study Summary
To assess the effects and safety of PF-00610355 on patients with chronic obstructive lung disease (COPD)
Conditions Studied
Interventions
- DRUG Placebo
- DRUG Salmeterol
- DRUG PF-00610355
- DRUG PF - 00610355
- DRUG PF- 00610355
Study Locations (20)
Florida
- Pfizer Investigational Site — Daytona Beach
- Pfizer Investigational Site — Ormond Beach
- Pfizer Investigational Site — Tampa
- Pfizer Investigational Site — Trinity
Minnesota
- Pfizer Investigational Site — Fridley
- Pfizer Investigational Site — Minneapolis
- Pfizer Investigational Site — Rochester
Ohio
- Pfizer Investigational Site — Cincinnati
- Pfizer Investigational Site — Cincinnati
- Pfizer Investigational Site — Cincinnati
California
- Pfizer Investigational Site — San Diego
- Pfizer Investigational Site — Spring Valley
Kansas
- Pfizer Investigational Site — Overland Park
- Pfizer Investigational Site — Overland Park
Alabama
- Pfizer Investigational Site — Fairhope
Colorado
- Pfizer Investigational Site — Wheat Ridge
Georgia
- Pfizer Investigational Site — Austell
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 405 participants |
| Start Date | 2010-03 |
| Est. Completion | 2010-12 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00808288
The ClinicalTrials.gov registry entry for NCT00808288 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 405 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pfizer, which has 769 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 Pulmonary Disease, Chronic Obstructive appearing as the primary indexed condition, and to 5 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: NCT00808288 reports 20 study locations spanning 11 distinct geographic areas — top geographies include Florida, Minnesota, Ohio. 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 NCT00808288 about?
NCT00808288 is a clinical study titled "A Study To Investigate The Safety, Toleration And Efficacy of PF00610355 In Chronic Obstructive Pulmonary Disease (COPD) Patients.". To assess the effects and safety of PF-00610355 on patients with chronic obstructive lung disease (COPD)
What is the current status of trial NCT00808288?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 405 participants. The study started on 2010-03. Estimated completion is 2010-12.
What conditions does trial NCT00808288 study?
This clinical trial studies the following conditions: Pulmonary Disease, Chronic Obstructive, Lung Diseases, Lung Diseases, Obstructive. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00808288?
The interventions under investigation include: Placebo (DRUG), Salmeterol (DRUG), PF-00610355 (DRUG), PF - 00610355 (DRUG), PF- 00610355 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00808288?
This trial is sponsored by Pfizer, which has 769 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00808288 being conducted?
This trial has 20 study locations across Alabama, California, Colorado, Florida, Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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