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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 Oct 28, 2026, 10:55 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 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.

Brief summary

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

Efficacy and safety of BI 1356 compared to placebo in patients with type 2 diabetes who have insufficient glycaemic control despite treatment 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

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
Dec 2008 (Type not available)
Primary completion
Jan 2010 (Actual)
Completion
Not listed
Last update posted
Jun 27, 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 27, 2014 · Synced Oct 28, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00819091 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →