Efficacy and Safety of BI 10773 in Combination With Insulin in Patients With Type 2 Diabetes

NCT ID: NCT01011868

Last Updated: 2014-09-30

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE2

Total Enrollment

494 participants

Study Classification

INTERVENTIONAL

Study Start Date

2009-11-30

Brief Summary

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The objective of the current study is to investigate the efficacy, safety and tolerability of BI 10773 at two different doses compared to placebo during long term treatment (78 weeks) in combination with basal insulin in patients with type 2 diabetes mellitus with insufficient glycaemic control.

Detailed Description

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Conditions

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Diabetes Mellitus, Type 2

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Study Groups

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BI 10773 low dose

Patients receive BI 10773 low dose daily

Group Type EXPERIMENTAL

BI 10773 low dose

Intervention Type DRUG

BI 10773 low dose

BI 10773 high dose

Patients receive BI 10773 high dose daily

Group Type EXPERIMENTAL

BI 10773 placebo

Intervention Type DRUG

BI 10773 placebo

BI 10773 high dose

Intervention Type DRUG

BI 10773 high dose

placebo

Patients receive placebo to match BI 10773 daily

Group Type PLACEBO_COMPARATOR

BI 10773 placebo

Intervention Type DRUG

BI 10773 placebo

Interventions

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BI 10773 placebo

BI 10773 placebo

Intervention Type DRUG

BI 10773 low dose

BI 10773 low dose

Intervention Type DRUG

BI 10773 high dose

BI 10773 high dose

Intervention Type DRUG

BI 10773 placebo

BI 10773 placebo

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

1. Signed and dated written informed consent by date of Visit 1 in accordance with Good Clinical Practice (GCP) and local legislation
2. Male and female patients with a diagnosis of Type 2 Diabetes Mellitus treated with a stable dose of basal insulin with or without concomitant metformin and / or sulfonylurea.
3. Glycosylated hemoglobin A1c (Type A, subtype 1c) of \>7.0% and \< or = 10% at Visit 1 (screening)
4. Suitability for trial participation according to investigator's judgment (evaluating all alternative treatment options and in consideration of the patient completing the study)
5. Age \> or =18 years at Visit 1 (screening)
6. BMI \< or = 45 kg/m2 (Body Mass Index) at Visit 1 (screening)

Exclusion Criteria

1. Patients with poorly controlled hyperglycemia
2. Frequent (at the discretion of the investigator) episodes of hypoglycemic events on basal insulin therapy
3. MI, stroke, or TIA within 3 months prior to obtaining informed consent
4. Impaired hepatic or renal function; gastric surgery; cancer within the last 5 years; blood dyscrasias

6\. Treatment with other anti-diabetics, anti-obesity medications, steroids or thyroid hormones, participation in another trial with an investigational drug 7. Pre-menopausal women on insufficient birth control 8. Alcohol or drug abuse
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Eli Lilly and Company

INDUSTRY

Sponsor Role collaborator

Boehringer Ingelheim

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Boehringer Ingelheim

Role: STUDY_CHAIR

Boehringer Ingelheim

Locations

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1245.33.01014 Boehringer Ingelheim Investigational Site

Birmingham, Alabama, United States

Site Status

1245.33.01047 Boehringer Ingelheim Investigational Site

Phoenix, Arizona, United States

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1245.33.01060 Boehringer Ingelheim Investigational Site

Fresno, California, United States

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1245.33.01013 Boehringer Ingelheim Investigational Site

Los Angeles, California, United States

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1245.33.01008 Boehringer Ingelheim Investigational Site

Los Gatos, California, United States

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1245.33.01019 Boehringer Ingelheim Investigational Site

National City, California, United States

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1245.33.01055 Boehringer Ingelheim Investigational Site

Paramount, California, United States

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1245.33.01012 Boehringer Ingelheim Investigational Site

Santa Ana, California, United States

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1245.33.01054 Boehringer Ingelheim Investigational Site

Denver, Colorado, United States

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1245.33.01046 Boehringer Ingelheim Investigational Site

Bradednton, Florida, United States

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1245.33.01050 Boehringer Ingelheim Investigational Site

Brooksville, Florida, United States

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1245.33.01059 Boehringer Ingelheim Investigational Site

Chiefland, Florida, United States

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1245.33.01028 Boehringer Ingelheim Investigational Site

Clearwater, Florida, United States

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1245.33.01029 Boehringer Ingelheim Investigational Site

Fleming Island, Florida, United States

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1245.33.01048 Boehringer Ingelheim Investigational Site

Hollywood, Florida, United States

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1245.33.01033 Boehringer Ingelheim Investigational Site

New Port Richey, Florida, United States

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1245.33.01027 Boehringer Ingelheim Investigational Site

Atlanta, Georgia, United States

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1245.33.01040 Boehringer Ingelheim Investigational Site

Decatur, Georgia, United States

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1245.33.01062 Boehringer Ingelheim Investigational Site

Lawrenceville, Georgia, United States

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1245.33.01020 Boehringer Ingelheim Investigational Site

Chicago, Illinois, United States

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1245.33.01044 Boehringer Ingelheim Investigational Site

Chicago, Illinois, United States

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1245.33.01024 Boehringer Ingelheim Investigational Site

Des Moines, Iowa, United States

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1245.33.01022 Boehringer Ingelheim Investigational Site

Saint Louis, Maryland, United States

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1245.33.01056 Boehringer Ingelheim Investigational Site

Olive Branch, Mississippi, United States

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1245.33.01032 Boehringer Ingelheim Investigational Site

Kansas City, Missouri, United States

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1245.33.01017 Boehringer Ingelheim Investigational Site

Omaha, Nebraska, United States

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1245.33.01043 Boehringer Ingelheim Investigational Site

Las Vegas, Nevada, United States

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1245.33.01051 Boehringer Ingelheim Investigational Site

New Hartford, New York, United States

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1245.33.01007 Boehringer Ingelheim Investigational Site

Greensboro, North Carolina, United States

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1245.33.01003 Boehringer Ingelheim Investigational Site

Jacksonville, North Carolina, United States

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1245.33.01016 Boehringer Ingelheim Investigational Site

Salisbury, North Carolina, United States

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1245.33.01005 Boehringer Ingelheim Investigational Site

Statesville, North Carolina, United States

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1245.33.01038 Boehringer Ingelheim Investigational Site

Wilmington, North Carolina, United States

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1245.33.01026 Boehringer Ingelheim Investigational Site

Winston-Salem, North Carolina, United States

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1245.33.01025 Boehringer Ingelheim Investigational Site

Cincinnati, Ohio, United States

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1245.33.01001 Boehringer Ingelheim Investigational Site

Columbus, Ohio, United States

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1245.33.01031 Boehringer Ingelheim Investigational Site

Tulsa, Oklahoma, United States

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1245.33.01045 Boehringer Ingelheim Investigational Site

Eugene, Oregon, United States

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1245.33.01018 Boehringer Ingelheim Investigational Site

Altoona, Pennsylvania, United States

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1245.33.01041 Boehringer Ingelheim Investigational Site

Carlisle, Pennsylvania, United States

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1245.33.01042 Boehringer Ingelheim Investigational Site

Landsdale, Pennsylvania, United States

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1245.33.01004 Boehringer Ingelheim Investigational Site

Greer, South Carolina, United States

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1245.33.01036 Boehringer Ingelheim Investigational Site

Mt. Pleasant, South Carolina, United States

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1245.33.01035 Boehringer Ingelheim Investigational Site

Seneca, South Carolina, United States

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1245.33.01058 Boehringer Ingelheim Investigational Site

Kingsport, Tennessee, United States

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1245.33.01037 Boehringer Ingelheim Investigational Site

Memphis, Tennessee, United States

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1245.33.01023 Boehringer Ingelheim Investigational Site

Dallas, Texas, United States

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1245.33.01030 Boehringer Ingelheim Investigational Site

Dallas, Texas, United States

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1245.33.01006 Boehringer Ingelheim Investigational Site

Houston, Texas, United States

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1245.33.01011 Boehringer Ingelheim Investigational Site

Houston, Texas, United States

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1245.33.01002 Boehringer Ingelheim Investigational Site

Sugar Land, Texas, United States

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1245.33.01049 Boehringer Ingelheim Investigational Site

Salt Lake City, Utah, United States

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1245.33.01015 Boehringer Ingelheim Investigational Site

Norfolk, Virginia, United States

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1245.33.01009 Boehringer Ingelheim Investigational Site

Richmond, Virginia, United States

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1245.33.01010 Boehringer Ingelheim Investigational Site

Federal Way, Washington, United States

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1245.33.01061 Boehringer Ingelheim Investigational Site

Milwaukee, Wisconsin, United States

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1245.33.45006 Boehringer Ingelheim Investigational Site

Aalborg, , Denmark

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1245.33.45001 Boehringer Ingelheim Investigational Site

Aarhus C, , Denmark

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1245.33.45011 Boehringer Ingelheim Investigational Site

Aarhus C, , Denmark

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1245.33.45013 Boehringer Ingelheim Investigational Site

Aarhus C, , Denmark

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1245.33.45004 Boehringer Ingelheim Investigational Site

Gentofte Municipality, , Denmark

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1245.33.45008 Boehringer Ingelheim Investigational Site

Hillerød, , Denmark

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1245.33.45002 Boehringer Ingelheim Investigational Site

Hvidovre, , Denmark

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1245.33.45003 Boehringer Ingelheim Investigational Site

København NV, , Denmark

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1245.33.3301A Boehringer Ingelheim Investigational Site

Bondy, , France

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1245.33.3302A Boehringer Ingelheim Investigational Site

Corbeil-Essonnes, , France

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1245.33.3305A Boehringer Ingelheim Investigational Site

La Rochelle, , France

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1245.33.3306A Boehringer Ingelheim Investigational Site

Marseille, , France

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1245.33.3308A Boehringer Ingelheim Investigational Site

Montbrison, , France

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1245.33.3309A Boehringer Ingelheim Investigational Site

Nanterre, , France

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1245.33.3310A Boehringer Ingelheim Investigational Site

Nantes, , France

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1245.33.3304A Boehringer Ingelheim Investigational Site

Narbonne, , France

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1245.33.3303A Boehringer Ingelheim Investigational Site

Saint-Mandé, , France

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1245.33.35302 Boehringer Ingelheim Investigational Site

Dublin, , Ireland

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1245.33.35303 Boehringer Ingelheim Investigational Site

Dublin, , Ireland

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1245.33.35304 Boehringer Ingelheim Investigational Site

Dublin, , Ireland

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1245.33.35104 Boehringer Ingelheim Investigational Site

Aveiro, , Portugal

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1245.33.35101 Boehringer Ingelheim Investigational Site

Coimbra, , Portugal

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1245.33.35102 Boehringer Ingelheim Investigational Site

Lisbon, , Portugal

Site Status

1245.33.35106 Boehringer Ingelheim Investigational Site

Lisbon, , Portugal

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1245.33.35107 Boehringer Ingelheim Investigational Site

Lisbon, , Portugal

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1245.33.82008 Boehringer Ingelheim Investigational Site

Daejeon, , South Korea

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1245.33.82007 Boehringer Ingelheim Investigational Site

Gwangju, , South Korea

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1245.33.82001 Boehringer Ingelheim Investigational Site

Seoul, , South Korea

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1245.33.82003 Boehringer Ingelheim Investigational Site

Seoul, , South Korea

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1245.33.82004 Boehringer Ingelheim Investigational Site

Seoul, , South Korea

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1245.33.82005 Boehringer Ingelheim Investigational Site

Seoul, , South Korea

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1245.33.82006 Boehringer Ingelheim Investigational Site

Wŏnju, , South Korea

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1245.33.82002 Boehringer Ingelheim Investigational Site

Yangsan, , South Korea

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1245.33.44001 Boehringer Ingelheim Investigational Site

Bath, , United Kingdom

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1245.33.44003 Boehringer Ingelheim Investigational Site

Birmingham, , United Kingdom

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1245.33.44006 Boehringer Ingelheim Investigational Site

Blackburn, , United Kingdom

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1245.33.44005 Boehringer Ingelheim Investigational Site

Dorking, , United Kingdom

Site Status

1245.33.44009 Boehringer Ingelheim Investigational Site

Headington, , United Kingdom

Site Status

1245.33.44008 Boehringer Ingelheim Investigational Site

Leicester, , United Kingdom

Site Status

1245.33.44004 Boehringer Ingelheim Investigational Site

Liverpool, , United Kingdom

Site Status

1245.33.44007 Boehringer Ingelheim Investigational Site

Wembley, , United Kingdom

Site Status

1245.33.44002 Boehringer Ingelheim Investigational Site

Whitstable, , United Kingdom

Site Status

1245.33.44010 Boehringer Ingelheim Investigational Site

Wymondham, , United Kingdom

Site Status

Countries

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United States Denmark France Ireland Portugal South Korea United Kingdom

References

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Tuttle KR, Levin A, Nangaku M, Kadowaki T, Agarwal R, Hauske SJ, Elsasser A, Ritter I, Steubl D, Wanner C, Wheeler DC. Safety of Empagliflozin in Patients With Type 2 Diabetes and Chronic Kidney Disease: Pooled Analysis of Placebo-Controlled Clinical Trials. Diabetes Care. 2022 Jun 2;45(6):1445-1452. doi: 10.2337/dc21-2034.

Reference Type DERIVED
PMID: 35472672 (View on PubMed)

Other Identifiers

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2009-013668-38

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

1245.33

Identifier Type: -

Identifier Source: org_study_id

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