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Completed Phase 2 Interventional Results available

Empagliflozin (BI 10773) in Type Two Diabetes (T2D) Patients, Open Label Extension

ClinicalTrials.gov ID: NCT00881530

Public ClinicalTrials.gov record NCT00881530. 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 21, 2026, 6:09 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 78 Week Open Label Extension to Trials Assessing the Safety and Efficacy of BI 10773 as Monotherapy or in Combination With Metformin in Type 2 Diabetic Patients

Brief summary

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

The objective of the current study is to investigate the safety and efficacy of BI 10773 in 2 different doses compared to Metformin or to Sitagliptin given for 78 weeks in different modalities of treatment in patients with type 2 diabetes mellitus.

Study identification

NCT ID
NCT00881530
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
660 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
Mar 2009 (Type not available)
Primary completion
May 2011 (Actual)
Completion
Not listed
Last update posted
Jun 16, 2014

Started 2009

United States locations

U.S. sites
12
U.S. states
8
U.S. cities
12
Facility City State ZIP Site status
1245.24.101001 Boehringer Ingelheim Investigational Site Mission Viejo California — —
1245.24.101028 Boehringer Ingelheim Investigational Site Spring Valley California — —
1245.24.101027 Boehringer Ingelheim Investigational Site Walnut Creek California — —
1245.24.101004 Boehringer Ingelheim Investigational Site Clearwarter Florida — —
1245.24.101005 Boehringer Ingelheim Investigational Site Miami Florida — —
1245.24.101024 Boehringer Ingelheim Investigational Site Saint Cloud Florida — —
1245.24.101014 Boehringer Ingelheim Investigational Site Roswell Georgia — —
1245.24.101016 Boehringer Ingelheim Investigational Site Staten Island New York — —
1245.24.101006 Boehringer Ingelheim Investigational Site Wadsworth Ohio — —
1245.24.101023 Boehringer Ingelheim Investigational Site Norristown Pennsylvania — —
1245.24.101015 Boehringer Ingelheim Investigational Site Dallas Texas — —
1245.24.101025 Boehringer Ingelheim Investigational Site Federal Way 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 125 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00881530, 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 16, 2014 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00881530 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →