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Completed Phase 2 Interventional

A Phase 2 Study of the Safety and Efficacy of a Tofimilast in Adult Patients With Chronic Obstructive Pulmonary Disease

ClinicalTrials.gov ID: NCT00219622

Public ClinicalTrials.gov record NCT00219622. 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 Sep 5, 2026, 5:01 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase 2, Randomized, Double-Blind, Placebo-Controlled, Six Week Study Of The Efficacy And Safety Of Tofimilast Dry Powder For Inhalation In Adults Diagnosed With Chronic Obstructive Pulmonary Disease

Brief summary

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

This an initial proof of concept, phase to study to assess the safety and efficacy of tofimilast for the chronic maintenance treatment of adults with Chronic Obstructive Pulmonary Disease

Study identification

NCT ID
NCT00219622
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
300 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 Years to 75 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
Apr 30, 2004
Primary completion
Jun 30, 2005
Completion
Jun 30, 2005
Last update posted
Nov 6, 2012

2004 – 2005

United States locations

U.S. sites
23
U.S. states
17
U.S. cities
21
Facility City State ZIP Site status
Pfizer Investigational Site Phoenix Arizona 85006
Pfizer Investigational Site Riverside California 92506
Pfizer Investigational Site Clearwater Florida 33756
Pfizer Investigational Site Clearwater Florida 33765
Pfizer Investigational Site Riverdale Georgia 30296
Pfizer Investigational Site Stockbridge Georgia 30281
Pfizer Investigational Site Normal Illinois 61761
Pfizer Investigational Site Iowa City Iowa 52240
Pfizer Investigational Site Madisonville Kentucky 42431
Pfizer Investigational Site Wheaton Maryland 20902
Pfizer Investigational Site Edina Minnesota 55438
Pfizer Investigational Site Minneapolis Minnesota 55407
Pfizer Investigational Site Buffalo New York 14215-1199
Pfizer Investigational Site Charlotte North Carolina 28207
Pfizer Investigational Site Cincinnati Ohio 45241
Pfizer Investigational Site Lake Oswego Oregon 97035
Pfizer Investigational Site Lincoln Rhode Island 02865
Pfizer Investigational Site Spartanburg South Carolina 29303
Pfizer Investigational Site Spartanburg South Carolina 29307
Pfizer Investigational Site Dallas Texas 75231
Pfizer Investigational Site Bellingham Washington 98226
Pfizer Investigational Site Renton Washington 98055
Pfizer Investigational Site Tukwila Washington 98188

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 17 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00219622, 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 Nov 6, 2012 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00219622 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →