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Completed Phase 3 Interventional Results available

Efficacy and Safety of Linagliptin in Combination With Insulin in Patients With Type 2 Diabetes

ClinicalTrials.gov ID: NCT00954447

Public ClinicalTrials.gov record NCT00954447. 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 19, 2026, 4:13 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 III Randomised, Double-blind, Placebo-controlled, Parallel Group Efficacy and Safety Study of Linagliptin (5 mg), Administered Orally Once Daily for at Least 52 Weeks in Type 2 Diabetic Patients in Combination With Basal Insulin Therapy

Brief summary

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

The objective of the current study is to investigate the efficacy, safety and tolerability of linagliptin (5 mg / once daily) compared to Placebo during long term treatment (52 weeks and longer) in combination with basal insulin in patients with type 2 diabetes mellitus with insufficient glycaemic control.

Study identification

NCT ID
NCT00954447
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
1,263 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Aug 2009 (Type not available)
Primary completion
Sep 2011 (Actual)
Completion
Not listed
Last update posted
Dec 30, 2013

Started 2009

United States locations

U.S. sites
47
U.S. states
21
U.S. cities
45
Facility City State ZIP Site status
1218.36.01043 Boehringer Ingelheim Investigational Site Escondido California — —
1218.36.01051 Boehringer Ingelheim Investigational Site Escondido California — —
1218.36.01065 Boehringer Ingelheim Investigational Site Fresno California — —
1218.36.01021 Boehringer Ingelheim Investigational Site Greenbrae California — —
1218.36.01013 Boehringer Ingelheim Investigational Site Los Angeles California — —
1218.36.01048 Boehringer Ingelheim Investigational Site Los Angeles California — —
1218.36.01058 Boehringer Ingelheim Investigational Site San Diego California — —
1218.36.01008 Boehringer Ingelheim Investigational Site Santa Ana California — —
1218.36.01056 Boehringer Ingelheim Investigational Site Waterbury Connecticut — —
1218.36.01054 Boehringer Ingelheim Investigational Site Clearwater Florida — —
1218.36.01035 Boehringer Ingelheim Investigational Site Inverness Florida — —
1218.36.01010 Boehringer Ingelheim Investigational Site Miami Florida — —
1218.36.01042 Boehringer Ingelheim Investigational Site New Port Richey Florida — —
1218.36.01063 Boehringer Ingelheim Investigational Site Pembroke Pines Florida — —
1218.36.01037 Boehringer Ingelheim Investigational Site Ponte Vedra Florida — —
1218.36.01032 Boehringer Ingelheim Investigational Site Saint Cloud Florida — —
1218.36.01049 Boehringer Ingelheim Investigational Site St. Petersburg Florida — —
1218.36.01036 Boehringer Ingelheim Investigational Site Atlanta Georgia — —
1218.36.01047 Boehringer Ingelheim Investigational Site Decatur Georgia — —
1218.36.01009 Boehringer Ingelheim Investigational Site Roswell Georgia — —
1218.36.01055 Boehringer Ingelheim Investigational Site Honolulu Hawaii — —
1218.36.01014 Boehringer Ingelheim Investigational Site Chicago Illinois — —
1218.36.01011 Boehringer Ingelheim Investigational Site Paducah Kentucky — —
1218.36.01034 Boehringer Ingelheim Investigational Site City of Saint Peters Missouri — —
1218.36.01040 Boehringer Ingelheim Investigational Site Kansas City Missouri — —
1218.36.01029 Boehringer Ingelheim Investigational Site St Louis Missouri — —
1218.36.01018 Boehringer Ingelheim Investigational Site Omaha Nebraska — —
1218.36.01053 Boehringer Ingelheim Investigational Site New Hartford New York — —
1218.36.01006 Boehringer Ingelheim Investigational Site Burlington North Carolina — —
1218.36.01025 Boehringer Ingelheim Investigational Site Hickory North Carolina — —
1218.36.01005 Boehringer Ingelheim Investigational Site Statesville North Carolina — —
1218.36.01015 Boehringer Ingelheim Investigational Site Cincinnati Ohio — —
1218.36.01039 Boehringer Ingelheim Investigational Site Tulsa Oklahoma — —
1218.36.01019 Boehringer Ingelheim Investigational Site Altoona Pennsylvania — —
1218.36.01012 Boehringer Ingelheim Investigational Site Norristown Pennsylvania — —
1218.36.01004 Boehringer Ingelheim Investigational Site Greer South Carolina — —
1218.36.01020 Boehringer Ingelheim Investigational Site Simpsonville South Carolina — —
1218.36.01003 Boehringer Ingelheim Investigational Site Kingsport Tennessee — —
1218.36.01038 Boehringer Ingelheim Investigational Site Dallas Texas — —
1218.36.01016 Boehringer Ingelheim Investigational Site Houston Texas — —
1218.36.01026 Boehringer Ingelheim Investigational Site Salt Lake City Utah — —
1218.36.01041 Boehringer Ingelheim Investigational Site Bennington Vermont — —
1218.36.01064 Boehringer Ingelheim Investigational Site Richmond Virginia — —
1218.36.01024 Boehringer Ingelheim Investigational Site Lakewood Washington — —
1218.36.01007 Boehringer Ingelheim Investigational Site Renton Washington — —
1218.36.01027 Boehringer Ingelheim Investigational Site Spokane Washington — —
1218.36.01062 Boehringer Ingelheim Investigational Site Tacoma Washington — —

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 122 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00954447, 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 Dec 30, 2013 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00954447 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →