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Completed Phase 3 Interventional Results available

Randomized, Double-blind (db), Placebo-controlled 18 Week Study of Linagliptin (BI 1356) in Type 2 Diabetic Patients With Insufficient Glycaemic Control on a Sulfonylurea Drug

ClinicalTrials.gov ID: NCT00819091

Public ClinicalTrials.gov record NCT00819091. 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 5, 2026, 3:56 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, Double-blind, Placebo-controlled Parallel Group Efficacy and Safety Study of BI 1356 (5 mg Administered Orally Once Daily) Over 18 Weeks in Type 2 Diabetic Patients With Insufficient Glycaemic Control (HbA1c 7.0-10%) Despite Background Therapy With a Sulfonylurea Drug.

Study identification

NCT ID
NCT00819091
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
245 participants

Conditions and interventions

Interventions

  • BI 1356 Drug
  • Placebo 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
Nov 30, 2008
Primary completion
Dec 31, 2009
Completion
Not listed
Last update posted
Jun 26, 2014

Started 2008

United States locations

U.S. sites
13
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
1218.35.10002 Boehringer Ingelheim Investigational Site Birmingham Alabama
1218.35.10001 Boehringer Ingelheim Investigational Site Los Angeles California
1218.35.10016 Boehringer Ingelheim Investigational Site National City California
1218.35.10017 Boehringer Ingelheim Investigational Site Fort Lauderdale Florida
1218.35.10021 Boehringer Ingelheim Investigational Site Fort Lauderdale Florida
1218.35.10013 Boehringer Ingelheim Investigational Site Chicago Illinois
1218.35.10015 Boehringer Ingelheim Investigational Site Flint Michigan
1218.35.10018 Boehringer Ingelheim Investigational Site Asheville North Carolina
1218.35.10004 Boehringer Ingelheim Investigational Site Cincinnati Ohio
1218.35.10005 Boehringer Ingelheim Investigational Site Portland Oregon
1218.35.10020 Boehringer Ingelheim Investigational Site Greenville South Carolina
1218.35.10009 Boehringer Ingelheim Investigational Site Dallas Texas
1218.35.10019 Boehringer Ingelheim Investigational Site Sugar Land Texas

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 32 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00819091, 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 26, 2014 · Synced May 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00819091 live on ClinicalTrials.gov.

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