Comparison of NN5401 Plus Insulin Aspart With Insulin Detemir Plus Insulin Aspart in Type 1 Diabetes



Status:Completed
Conditions:Diabetes, Diabetes
Therapuetic Areas:Endocrinology
Healthy:No
Age Range:18 - Any
Updated:4/21/2016
Start Date:August 2009
End Date:December 2010

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NN5401-3594: A 26-week, Open-labelled, Two-arm, Parallel, Randomised Trial Comparing Efficacy and Safety of NN5401 Once Daily Plus Insulin Aspart vs. Basal-bolus Treatment With Insulin Detemir Plus Insulin Aspart in Subjects With Type 1 Diabetes / NN5401-3645: An Extension Trial Comparing Safety and Efficacy of NN5401 Plus Meal-time Insulin Aspart for the Remaining Meals With Insulin Detemir Plus Meal-time Insulin Aspart in Type 1 Diabetes (BOOST™: T1)

This trial is conducted in Europe, Oceania, and the United States of America (USA).

The aim of this clinical trial is to compare NN5401 (insulin degludec/insulin aspart
(IDegAsp)) with insulin detemir (IDet) plus insulin aspart in patients with type 1 diabetes
(main period) followed by the extension period comparing the long-term safety of NN5401 plus
insulin aspart with insulin detemir plus insulin aspart.

The main period is registered internally at Novo Nordisk as NN5401-3594 while the extension
period is registered as NN5401-3645.


Inclusion Criteria:

- FOR THE MAIN TRIAL, NN5401-3594:

- Type 1 diabetes mellitus for at least 12 months

- Ongoing daily treatment with insulin (in a basal bolus regimen, premix insulin
regimen, self mix regimen) for at least 12 months

- HbA1c 7.0-10.0% (both inclusive)

- BMI (Body Mass Index) below or equal to 35.0 kg/m^2

- FOR THE EXTENSION TRIAL, NN5401-3645:

- The subject must have completed the six-month treatment period in trial NN5401-3594

Exclusion Criteria:

- FOR THE MAIN TRIAL, NN5401-3594:

- Treatment with other insulin regimens than insulin in a basal bolus regimen/premix
insulin regimen/self mix regimen within 3 months

- Cardiovascular disease within the last 6 months

- Uncontrolled treated/untreated severe hypertension

- Pregnancy, breast-feeding, the intention of becoming pregnant or not using adequate
contraceptive measures according to local requirements

- Cancer and medical history of cancer

- FOR THE EXTENSION TRIAL, NN5401-3645:

- Anticipated significant lifestyle changes during the trial

- Pregnancy, breast-feeding, the intention of becoming pregnant or not using adequate
contraceptive measures
We found this trial at
28
sites
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Atlanta, GA
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Butte, MT
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Chicago, Illinois 60607
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Chicago, IL
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Dallas, TX
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Eagan, MN
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Geelong,
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Greer, South Carolina 29651
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Greer, SC
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Henderson, Nevada 89052
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Henderson, NV
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Honolulu, HI
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La Mesa, California 91942
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La Mesa, CA
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Lancaster, California 93534
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Lancaster, CA
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Lawrenceville, Georgia 30046
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Lawrenceville, GA
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Lexington, Kentucky 40503
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Lexington, KY
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Miami, FL
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Minneapolis, Minnesota 55416
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Minneapolis, MN
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Mission Hills, California 91345
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Mission Hills, CA
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Morehead City, North Carolina 28557
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Morehead City, NC
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North Hollywood, California 91606
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North Hollywood, CA
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Omaha, NE
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Roswell, GA
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Salinas, California 93901
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Salinas, CA
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San Antonio, Texas 78229
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San Antonio, TX
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Seattle, Washington 98122
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Seattle, WA
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Shawnee Mission, Kansas 66204
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Shawnee Mission, KS
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St. Peters, Missouri 63376
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Valencia, California 91355
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Valencia, CA
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