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Completed Phase 3 Interventional Results available

Exubera vs Lispro in a Lantus-based Regimen for Improved Glycemic Control in Type 2 Diabetes

ClinicalTrials.gov ID: NCT00348374

Public ClinicalTrials.gov record NCT00348374. 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 17, 2026, 11:55 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 3b, Randomized, Open-Label, Parallel Group, Multicenter Trial Assessing The Efficacy Of Exubera Vs. Lispro Introduced Into A Lantus Based Regimen In Suboptimally Controlled Patients With Type 2 Diabetes Mellitus

Brief summary

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

The current trial will examine the efficacy and safety of Exubera administered as a mealtime insulin compared to lispro, when added to an existing regimen of basal insulin glargine + or = Oral Agents (OAs). Dose titrations will be provided which should allow a large proportion of subjects to reach target glycosylated hemoglobin (A1C) levels.

Study identification

NCT ID
NCT00348374
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer
Industry
Enrollment
191 participants

Conditions and interventions

Interventions

Drug

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
Jun 2006 (Type not available)
Primary completion
Aug 2008 (Actual)
Completion
Aug 2008 (Actual)
Last update posted
Mar 16, 2010

2006 – 2008

United States locations

U.S. sites
62
U.S. states
33
U.S. cities
58
Facility City State ZIP Site status
Pfizer Investigational Site Birmingham Alabama 35294-307 —
Pfizer Investigational Site Mobile Alabama 36608 —
Pfizer Investigational Site Phoenix Arizona 85006-2850 —
Pfizer Investigational Site Malvern Arkansas 72104 —
Pfizer Investigational Site Foot Hill Ranch California 92610 —
Pfizer Investigational Site Fresno California 93720 —
Pfizer Investigational Site Greenbrae California 94904 —
Pfizer Investigational Site Los Gatos California 95032-3739 —
Pfizer Investigational Site San Diego California 92120 —
Pfizer Investigational Site San Mateo California 94401-3805 —
Pfizer Investigational Site Tustin California 92780 —
Pfizer Investigational Site Denver Colorado 80209 —
Pfizer Investigational Site New Britain Connecticut 06050 —
Pfizer Investigational Site Washington D.C. District of Columbia 20010-2934 —
Pfizer Investigational Site Jacksonville Florida 32205 —
Pfizer Investigational Site Jacksonville Florida 32216 —
Pfizer Investigational Site Miami Florida 33156 —
Pfizer Investigational Site West Palm Beach Florida 33401 —
Pfizer Investigational Site Winter Park Florida 32789 —
Pfizer Investigational Site Columbus Georgia 31904 —
Pfizer Investigational Site Decatur Georgia 30034-1680 —
Pfizer Investigational Site Honolulu Hawaii 96813 —
Pfizer Investigational Site Honululu Hawaii 96814 —
Pfizer Investigational Site Idaho Falls Idaho 83404 —
Pfizer Investigational Site Chicago Illinois 60607 —
Pfizer Investigational Site Gurnee Illinois 60031 —
Pfizer Investigational Site Des Moines Iowa 50314 —
Pfizer Investigational Site Lexington Kentucky 40503 —
Pfizer Investigational Site Louisville Kentucky 40213 —
Pfizer Investigational Site Baltimore Maryland 21234-4607 —
Pfizer Investigational Site Bethesda Maryland 20817 —
Pfizer Investigational Site Boston Massachusetts 02114 —
Pfizer Investigational Site Flint Michigan 48532 —
Pfizer Investigational Site Minneapolis Minnesota 55454-1321 —
Pfizer Investigational Site St Louis Missouri 63110 —
Pfizer Investigational Site St Louis Missouri 63141 —
Pfizer Investigational Site Omaha Nebraska 68131 —
Pfizer Investigational Site East Syracuse New York 13057 —
Pfizer Investigational Site Greenville North Carolina 27834 —
Pfizer Investigational Site Morehead City North Carolina 28557 —
Pfizer Investigational Site Statesville North Carolina 28625 —
Pfizer Investigational Site Kettering Ohio 45429 —
Pfizer Investigational Site Oklahoma City Oklahoma 73103 —
Pfizer Investigational Site Tulsa Oklahoma 74104 —
Pfizer Investigational Site Bend Oregon 97701 —
Pfizer Investigational Site Bensalem Pennsylvania 19020 —
Pfizer Investigational Site Greenville South Carolina 29615 —
Pfizer Investigational Site Bartlett Tennessee 38133 —
Pfizer Investigational Site Memphis Tennessee 38119 —
Pfizer Investigational Site Arlington Texas 76012 —
Pfizer Investigational Site Arlington Texas 76014 —
Pfizer Investigational Site Dallas Texas 75230 —
Pfizer Investigational Site Dallas Texas 75246 —
Pfizer Investigational Site El Paso Texas 79935 —
Pfizer Investigational Site Houston Texas 77004 —
Pfizer Investigational Site San Antonio Texas 78229 —
Pfizer Investigational Site Bennington Vermont 05201-5018 —
Pfizer Investigational Site Norfolk Virginia 23502 —
Pfizer Investigational Site Virginia Beach Virginia 23462 —
Pfizer Investigational Site Renton Washington 98055 —
Pfizer Investigational Site Spokane Washington 99208 —
Pfizer Investigational Site Milwaukee Wisconsin 53209 —

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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00348374, 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 Mar 16, 2010 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00348374 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →