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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00219622
Other study ID # A2641022
Secondary ID
Status Completed
Phase Phase 2
First received September 11, 2005
Last updated November 5, 2012
Start date May 2004
Est. completion date July 2005

Study information

Verified date November 2012
Source Pfizer
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

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


Recruitment information / eligibility

Status Completed
Enrollment 300
Est. completion date July 2005
Est. primary completion date July 2005
Accepts healthy volunteers No
Gender Both
Age group 40 Years to 75 Years
Eligibility Inclusion Criteria:

- Moderate-severe COPD (GOLD 2003 definition)

- Smoking history of at least 10 pack-years

Exclusion Criteria:

- Any significant co-morbid disease, particularly cardiovascular

- Use of any maintenance therapy except short acting bronchodilators

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
tofimilast


Locations

Country Name City State
Argentina Pfizer Investigational Site Buenos Aires
Argentina Pfizer Investigational Site Buenos Aires
Argentina Pfizer Investigational Site Buenos Aires
Argentina Pfizer Investigational Site La Plata Buenos Aires
Argentina Pfizer Investigational Site Rosario Santa Fe
Argentina Pfizer Investigational Site Vicente Lopez Buenos Aires
Brazil Pfizer Investigational Site Curitiba PR
Brazil Pfizer Investigational Site Porto Alegre RS
Brazil Pfizer Investigational Site Porto Alegre RS
Chile Pfizer Investigational Site Providencia Santiago
Chile Pfizer Investigational Site Recoleta Santiago
Chile Pfizer Investigational Site Santiago
Chile Pfizer Investigational Site ValparaÃ-so
Costa Rica Pfizer Investigational Site San Jose
Mexico Pfizer Investigational Site México D.f.
Mexico Pfizer Investigational Site Monterrey Nuevo Leon
Mexico Pfizer Investigational Site Monterrey Nuevo León
United States Pfizer Investigational Site Bellingham Washington
United States Pfizer Investigational Site Buffalo New York
United States Pfizer Investigational Site Charlotte North Carolina
United States Pfizer Investigational Site Cincinnati Ohio
United States Pfizer Investigational Site Clearwater Florida
United States Pfizer Investigational Site Clearwater Florida
United States Pfizer Investigational Site Dallas Texas
United States Pfizer Investigational Site Edina Minnesota
United States Pfizer Investigational Site Iowa City Iowa
United States Pfizer Investigational Site Lake Oswego Oregon
United States Pfizer Investigational Site Lincoln Rhode Island
United States Pfizer Investigational Site Madisonville Kentucky
United States Pfizer Investigational Site Minneapolis Minnesota
United States Pfizer Investigational Site Normal Illinois
United States Pfizer Investigational Site Phoenix Arizona
United States Pfizer Investigational Site Renton Washington
United States Pfizer Investigational Site Riverdale Georgia
United States Pfizer Investigational Site Riverside California
United States Pfizer Investigational Site Spartanburg South Carolina
United States Pfizer Investigational Site Spartanburg South Carolina
United States Pfizer Investigational Site Stockbridge Georgia
United States Pfizer Investigational Site Tukwila Washington
United States Pfizer Investigational Site Wheaton Maryland

Sponsors (1)

Lead Sponsor Collaborator
Pfizer

Countries where clinical trial is conducted

United States,  Argentina,  Brazil,  Chile,  Costa Rica,  Mexico, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline in FEV1 compared to placebo
Secondary Change from baseline in other lung function parameters, dyspnea, quality of life compared to placebo
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