Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

Safety and Efficacy of Empagliflozin (BI 10773) and Sitagliptin Versus Placebo Over 76 Weeks in Patients With Type 2 Diabetes

ClinicalTrials.gov ID: NCT01289990

Public ClinicalTrials.gov record NCT01289990. 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 Sep 1, 2026, 2:56 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 Double-blind, Extension, Placebo-controlled Parallel Group Safety and Efficacy Trial of BI 10773 (10 and 25mg Once Daily) and Sitagliptin (100mg Once Daily) Given for Minimum 76 Weeks (Incl. 24 Weeks of Preceding Trial) as Monotherapy or With Different Back-ground Therapies in Patients With Type 2 Diabetes Mellitus Previously Completing Trial 1245.19, 1245.20 or 1245.23

Brief summary

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

This study will investigate the efficacy and long term safety and tolerability of BI 10773 in type 2 diabetic patients.

Study identification

NCT ID
NCT01289990
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
2,705 participants

Conditions and interventions

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
Jan 31, 2011
Primary completion
Apr 30, 2013
Completion
Apr 30, 2013
Last update posted
Jul 14, 2014

2011 – 2013

United States locations

U.S. sites
40
U.S. states
18
U.S. cities
39
Facility City State ZIP Site status
1245.31.10145 Boehringer Ingelheim Investigational Site Birmingham Alabama
1245.31.10162 Boehringer Ingelheim Investigational Site Glendale Arizona
1245.31.10124 Boehringer Ingelheim Investigational Site Mesa Arizona
1245.31.10108 Boehringer Ingelheim Investigational Site Phoenix Arizona
1245.31.10046 Boehringer Ingelheim Investigational Site Tempe Arizona
1245.31.10154 Boehringer Ingelheim Investigational Site Chino California
1245.31.10149 Boehringer Ingelheim Investigational Site Rancho Cucamonga California
1245.31.10131 Boehringer Ingelheim Investigational Site West Hills California
1245.31.10038 Boehringer Ingelheim Investigational Site Northglenn Colorado
1245.31.10127 Boehringer Ingelheim Investigational Site Waterbury Connecticut
1245.31.10137 Boehringer Ingelheim Investigational Site Clearwater Florida
1245.31.10133 Boehringer Ingelheim Investigational Site Jupiter Florida
1245.31.10006 Boehringer Ingelheim Investigational Site Miami Florida
1245.31.10085 Boehringer Ingelheim Investigational Site Plantation Florida
1245.31.10080 Boehringer Ingelheim Investigational Site Decatur Georgia
1245.31.10077 Boehringer Ingelheim Investigational Site Perry Georgia
1245.31.10001 Boehringer Ingelheim Investigational Site Chicago Illinois
1245.31.10159 Boehringer Ingelheim Investigational Site Des Moines Iowa
1245.31.10014 Boehringer Ingelheim Investigational Site Dubuque Iowa
1245.31.10117 Boehringer Ingelheim Investigational Site Arkansas City Kansas
1245.31.10157 Boehringer Ingelheim Investigational Site Newton Kansas
1245.31.10146 Boehringer Ingelheim Investigational Site Louisville Kentucky
1245.31.10003 Boehringer Ingelheim Investigational Site Dearborn Michigan
1245.31.10059 Boehringer Ingelheim Investigational Site New Hyde Park New York
1245.31.10034 Boehringer Ingelheim Investigational Site Rochester New York
1245.31.10123 Boehringer Ingelheim Investigational Site Smithtown New York
1245.31.10071 Boehringer Ingelheim Investigational Site Asheboro North Carolina
1245.31.10086 Boehringer Ingelheim Investigational Site Salisbury North Carolina
1245.31.10129 Boehringer Ingelheim Investigational Site Carlisle Ohio
1245.31.10045 Boehringer Ingelheim Investigational Site Cincinnati Ohio
1245.31.10119 Boehringer Ingelheim Investigational Site Cincinnati Ohio
1245.31.10130 Boehringer Ingelheim Investigational Site Gallipolis Ohio
1245.31.10158 Boehringer Ingelheim Investigational Site Mt. Pleasant South Carolina
1245.31.10015 Boehringer Ingelheim Investigational Site Simpsonville South Carolina
1245.31.10033 Boehringer Ingelheim Investigational Site Chattanooga Tennessee
1245.31.10112 Boehringer Ingelheim Investigational Site Memphis Tennessee
1245.31.10156 Boehringer Ingelheim Investigational Site Houston Texas
1245.31.10151 Boehringer Ingelheim Investigational Site Hurst Texas
1245.31.10143 Boehringer Ingelheim Investigational Site Killeen Texas
1245.31.10155 Boehringer Ingelheim Investigational Site San Antonio 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 203 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01289990, 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 Jul 14, 2014 · Synced Sep 1, 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 protocol, eligibility criteria, and contact information for NCT01289990 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →