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Completed Phase 3 Interventional Results available

12 Week Efficacy and Safety Study of Empagliflozin (BI 10773) in Hypertensive Patients With Type 2 Diabetes Mellitus

ClinicalTrials.gov ID: NCT01370005

Public ClinicalTrials.gov record NCT01370005. 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 Nov 11, 2026, 3:08 AM EST

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Official title

A Phase III Randomised, Double-blind, Placebo-controlled, Parallel Group, Efficacy and Safety Study of BI 10773 (10 mg, 25 mg) Administered Orally, Once Daily Over 12 Weeks in Hypertensive Patients With Type 2 Diabetes Mellitus

Brief summary

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

This trial will evaluate safety and efficacy of BI 10773 in hypertensive patients with type 2 diabetes. Since hyperglycaemia and hypertension are key risk factors for both micro- and macrovascular complications, assessment of both glucose and blood pressure lowering effects of BI 10773 in hypertensive patients with type 2 diabetes could provide clinically highly relevant, new information for the use of BI 10773

Study identification

NCT ID
NCT01370005
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
825 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
Jun 2011 (Type not available)
Primary completion
Jul 2012 (Actual)
Completion
Jul 2012 (Actual)
Last update posted
Feb 22, 2016

2011 – 2012

United States locations

U.S. sites
35
U.S. states
15
U.S. cities
32
Facility City State ZIP Site status
1245.48.10024 Boehringer Ingelheim Investigational Site Huntsville Alabama — —
1245.48.10002 Boehringer Ingelheim Investigational Site Phoenix Arizona — —
1245.48.10014 Boehringer Ingelheim Investigational Site Lincoln California — —
1245.48.10030 Boehringer Ingelheim Investigational Site Long Beach California — —
1245.48.10033 Boehringer Ingelheim Investigational Site Long Beach California — —
1245.48.10027 Boehringer Ingelheim Investigational Site Los Angeles California — —
1245.48.10041 Boehringer Ingelheim Investigational Site Tustin California — —
1245.48.10039 Boehringer Ingelheim Investigational Site West Hills California — —
1245.48.10008 Boehringer Ingelheim Investigational Site Davie Florida — —
1245.48.10025 Boehringer Ingelheim Investigational Site Edgewater Florida — —
1245.48.10001 Boehringer Ingelheim Investigational Site Jacksonville Florida — —
1245.48.10016 Boehringer Ingelheim Investigational Site Miami Florida — —
1245.48.10035 Boehringer Ingelheim Investigational Site Palm Harbor Florida — —
1245.48.10018 Boehringer Ingelheim Investigational Site Pensacola Florida — —
1245.48.10032 Boehringer Ingelheim Investigational Site Pinellas Park Florida — —
1245.48.10012 Boehringer Ingelheim Investigational Site Marietta Georgia — —
1245.48.10011 Boehringer Ingelheim Investigational Site Addison Illinois — —
1245.48.10019 Boehringer Ingelheim Investigational Site Arlington Heights Illinois — —
1245.48.10022 Boehringer Ingelheim Investigational Site Chicago Illinois — —
1245.48.10017 Boehringer Ingelheim Investigational Site Wichita Kansas — —
1245.48.10010 Boehringer Ingelheim Investigational Site Albuquerque New Mexico — —
1245.48.10036 Boehringer Ingelheim Investigational Site Charlotte North Carolina — —
1245.48.10005 Boehringer Ingelheim Investigational Site Akron Ohio — —
1245.48.10004 Boehringer Ingelheim Investigational Site Kettering Ohio — —
1245.48.10013 Boehringer Ingelheim Investigational Site Erie Pennsylvania — —
1245.48.10020 Boehringer Ingelheim Investigational Site Pittsburgh Pennsylvania — —
1245.48.10029 Boehringer Ingelheim Investigational Site Knoxville Tennessee — —
1245.48.10015 Boehringer Ingelheim Investigational Site Memphis Tennessee — —
1245.48.10034 Boehringer Ingelheim Investigational Site Dallas Texas — —
1245.48.10007 Boehringer Ingelheim Investigational Site Houston Texas — —
1245.48.10009 Boehringer Ingelheim Investigational Site Houston Texas — —
1245.48.10042 Boehringer Ingelheim Investigational Site Houston Texas — —
1245.48.10026 Boehringer Ingelheim Investigational Site San Antonio Texas — —
1245.48.10003 Boehringer Ingelheim Investigational Site Orem Utah — —
1245.48.10023 Boehringer Ingelheim Investigational Site Port Orchard 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 85 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01370005, 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 Feb 22, 2016 · Synced Nov 11, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01370005 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →