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Completed Phase 2 Interventional

A Study To Investigate The Safety, Toleration And Efficacy of PF00610355 In Chronic Obstructive Pulmonary Disease (COPD) Patients.

ClinicalTrials.gov ID: NCT00808288

Public ClinicalTrials.gov record NCT00808288. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 4, 2026, 9:39 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2b, Parallel Group, Placebo And Active Comparator Controlled Study To Investigate The Safety, Toleration And Efficacy Of 6-Week Once Daily Administration Of Inhaled PF-00610355 Dry Powder In Patients With Moderate Chronic Obstructive Pulmonary Disease.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

To assess the effects and safety of PF-00610355 on patients with chronic obstructive lung disease (COPD)

Study identification

NCT ID
NCT00808288
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
405 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 Years to 80 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 2010 (Type not available)
Primary completion
Dec 2010 (Actual)
Completion
Dec 2010 (Actual)
Last update posted
Feb 6, 2019

2010

United States locations

U.S. sites
30
U.S. states
16
U.S. cities
25
Facility City State ZIP Site status
Pfizer Investigational Site Fairhope Alabama 36532 —
Pfizer Investigational Site San Diego California 92120 —
Pfizer Investigational Site Spring Valley California 91978 —
Pfizer Investigational Site Wheat Ridge Colorado 80033 —
Pfizer Investigational Site Daytona Beach Florida 32114 —
Pfizer Investigational Site Ormond Beach Florida 32174 —
Pfizer Investigational Site Tampa Florida 33613 —
Pfizer Investigational Site Trinity Florida 34655 —
Pfizer Investigational Site Austell Georgia 30106 —
Pfizer Investigational Site Overland Park Kansas 66211 —
Pfizer Investigational Site Overland Park Kansas 66212 —
Pfizer Investigational Site Fridley Minnesota 55432 —
Pfizer Investigational Site Minneapolis Minnesota 55407 —
Pfizer Investigational Site Rochester Minnesota 55905 —
Pfizer Investigational Site St Louis Missouri 63141 —
Pfizer Investigational Site Rochester New York 14618 —
Pfizer Investigational Site Charlotte North Carolina 28207 —
Pfizer Investigational Site Cincinnati Ohio 45227 —
Pfizer Investigational Site Cincinnati Ohio 45231 —
Pfizer Investigational Site Cincinnati Ohio 45242 —
Pfizer Investigational Site Cincinnati Ohio 45245 —
Pfizer Investigational Site Oklahoma City Oklahoma 73112 —
Pfizer Investigational Site Lincoln Rhode Island 02865 —
Pfizer Investigational Site Pawtucket Rhode Island 02860 —
Pfizer Investigational Site Charleston South Carolina 29407 —
Pfizer Investigational Site Charleston South Carolina 29414 —
Pfizer Investigational Site Columbia South Carolina 29204 —
Pfizer Investigational Site Houston Texas 77030 —
Pfizer Investigational Site San Antonio Texas 78212 —
Pfizer Investigational Site Morgantown West Virginia 26505 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 45 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00808288, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 6, 2019 · Synced Nov 4, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00808288 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →