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Completed Phase 2 Interventional

A Study of the Safety and Efficacy of Tofimilast in Adult Asthmatics

ClinicalTrials.gov ID: NCT00150397

Public ClinicalTrials.gov record NCT00150397. 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 6, 2026, 6:12 AM EDT

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

Official title

A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Six-Week Study Of The Efficacy And Safety Of Tofimilast Dry Powder For Inhalation In Adults With Persistent Asthma

Brief summary

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

This is an initial proof of concept, phase to study to assess the safety and efficacy tofimilast for the chronic maintenance treatment of adults with persistent asthma

Study identification

NCT ID
NCT00150397
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
112 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 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
Feb 28, 2005
Primary completion
Oct 31, 2005
Completion
Oct 31, 2005
Last update posted
Jun 7, 2012

2005

United States locations

U.S. sites
16
U.S. states
13
U.S. cities
16
Facility City State ZIP Site status
Pfizer Investigational Site Encinitas California 92024
Pfizer Investigational Site Riverside California 92506
Pfizer Investigational Site DeLand Florida 32720
Pfizer Investigational Site Atlanta Georgia 30281
Pfizer Investigational Site Normal Illinois 61761
Pfizer Investigational Site Madisonville Kentucky 42431
Pfizer Investigational Site North Dartmouth Massachusetts 02747
Pfizer Investigational Site Springfield Massachusetts 01107
Pfizer Investigational Site Minneapolis Minnesota 55402
Pfizer Investigational Site Skillman New Jersey 08558
Pfizer Investigational Site Cincinnati Ohio 45241
Pfizer Investigational Site Lincoln Rhode Island 02865
Pfizer Investigational Site Kingsport Tennessee 37660
Pfizer Investigational Site Nashville Tennessee 37203
Pfizer Investigational Site Dallas Texas 75231
Pfizer Investigational Site Madison Wisconsin 53792

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 6 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00150397, 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 Jun 7, 2012 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00150397 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →