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Completed Phase 2 Interventional Results available

BI 10773 add-on to Metformin in Patients With Type 2 Diabetes

ClinicalTrials.gov ID: NCT00749190

Public ClinicalTrials.gov record NCT00749190. 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, 7:20 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 II, Randomized, Parallel Group Safety, Efficacy, and Pharmacokinetics Study of BI 10773 (1 mg, 5 mg, 10 mg, 25 mg, and 50 mg) Administered Orally Once Daily Over 12 Weeks Compared Double Blind to Placebo With an Additional Open-label Sitagliptin Arm in Type 2 Diabetic Patients With Insufficient Glycemic Control Despite Metformin 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 pharmacokinetics of five doses of BI 10773 compared to placebo given for 12 weeks as add-on therapy to on going metformin therapy in patients with T2DM with insufficient glycemic control. In addition, there will be an open-label treatment arm with sitagliptin (JanuviaTM) as add-on therapy to metformin.

Study identification

NCT ID
NCT00749190
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
495 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 79 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
Aug 2008 (Type not available)
Primary completion
Oct 2009 (Actual)
Completion
Not listed
Last update posted
Jun 13, 2014

Started 2008

United States locations

U.S. sites
19
U.S. states
10
U.S. cities
18
Facility City State ZIP Site status
1245.10.10026 Boehringer Ingelheim Investigational Site Chula Vista California — —
1245.10.10001 Boehringer Ingelheim Investigational Site Mission Viejo California — —
1245.10.10011 Boehringer Ingelheim Investigational Site Pasadena California — —
1245.10.10028 Boehringer Ingelheim Investigational Site Spring Valley California — —
1245.10.10027 Boehringer Ingelheim Investigational Site Walnut Creek California — —
1245.10.10004 Boehringer Ingelheim Investigational Site Clearwarter Florida — —
1245.10.10021 Boehringer Ingelheim Investigational Site Melbourne Florida — —
1245.10.10005 Boehringer Ingelheim Investigational Site Miami Florida — —
1245.10.10019 Boehringer Ingelheim Investigational Site Miami Florida — —
1245.10.10024 Boehringer Ingelheim Investigational Site Saint Cloud Florida — —
1245.10.10014 Boehringer Ingelheim Investigational Site Roswell Georgia — —
1245.10.10016 Boehringer Ingelheim Investigational Site Staten Island New York — —
1245.10.10009 Boehringer Ingelheim Investigational Site Shelby North Carolina — —
1245.10.10006 Boehringer Ingelheim Investigational Site Wadsworth Ohio — —
1245.10.10023 Boehringer Ingelheim Investigational Site Norristown Pennsylvania — —
1245.10.10010 Boehringer Ingelheim Investigational Site Clemson South Carolina — —
1245.10.10015 Boehringer Ingelheim Investigational Site Dallas Texas — —
1245.10.10012 Boehringer Ingelheim Investigational Site Temple Texas — —
1245.10.10025 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 97 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00749190, 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 13, 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 NCT00749190 live on ClinicalTrials.gov.

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