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Completed Phase 3 Interventional

US Inhaled Insulin Dose Titration Study

ClinicalTrials.gov ID: NCT00246623

Public ClinicalTrials.gov record NCT00246623. 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 Oct 28, 2026, 1:07 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 Randomized, Open-Label, Multicenter Study Assessing the Effects of Forced Exubera Dose Titration on Glycemic Control in Patients With Suboptimally Controlled Type 2 Diabetes on Two or More Oral Antidiabetic Agents

Brief summary

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

This study will examine how to dose Exubera (inhaled insulin) in patients who are not well controlled on two or more diabetes pills. This study should show that a large number of patients enrolled in the study can reach the target Hemoglobin A1C levels (7% or less) that have been set by the American Diabetes Association (ADA). Target goals should be achieved by adjusting the Exubera dose either weekly or twice weekly. Patients will also receive nutritional counseling and diabetes education as part of the study.

Study identification

NCT ID
NCT00246623
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer
Industry
Enrollment
120 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 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
Nov 2005 (Type not available)
Primary completion
Not listed
Completion
Mar 2007 (Actual)
Last update posted
Feb 8, 2008

2005 – 2007

United States locations

U.S. sites
16
U.S. states
11
U.S. cities
16
Facility City State ZIP Site status
Pfizer Investigational Site Birmingham Alabama — —
Pfizer Investigational Site Los Angeles California — —
Pfizer Investigational Site New Britain Connecticut — —
Pfizer Investigational Site Norwalk Connecticut — —
Pfizer Investigational Site Hollywood Florida — —
Pfizer Investigational Site Atlanta Georgia — —
Pfizer Investigational Site Boise Idaho — —
Pfizer Investigational Site Hayden Idaho — —
Pfizer Investigational Site Baton Rouge Louisiana — —
Pfizer Investigational Site Boston Massachusetts — —
Pfizer Investigational Site Albany New York — —
Pfizer Investigational Site Syracuse New York — —
Pfizer Investigational Site Dallas Texas — —
Pfizer Investigational Site El Paso Texas — —
Pfizer Investigational Site San Antonio Texas — —
Pfizer Investigational Site Bennington Vermont — —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00246623, 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 8, 2008 · Synced Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00246623 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →