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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 May 7, 2026, 1:17 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

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

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

  • Exubera Drug
  • Insulin Lispro Drug

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
May 31, 2006
Primary completion
Jul 31, 2008
Completion
Jul 31, 2008
Last update posted
Mar 15, 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 15, 2010 · Synced May 7, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00348374 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →