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Generated: February 19, 2019

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CLINICAL TRIALS PROFILE FOR TRESIBA

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Clinical Trials for Tresiba

Trial ID Title Status Sponsor Phase Summary
NCT01984372 Post-marketing Surveillance (Special Use-results Surveillance) on Long-term Use With Tresiba® Active, not recruiting Novo Nordisk A/S N/A This study is conducted in Asia. The aim of this post marketing surveillance (PMS) is to assess safety and effectiveness of long-term treatment with Tresiba® (insulin degludec) in patients with diabetes mellitus requiring insulin therapy under normal clinical practice conditions. A total of 4000 patients will be enrolled to investigate long term (3 years of treatment) safety of Tresiba® and additional 2000 patients will be enrolled to assess the safety in an early stage of the PMS more precisely. At the time of enrolment the patients will be randomly allocated to either 3 years or 6 months observation group.
NCT02117622 A Non-interventional, Post Marketing Surveillance (PMS) Study of Tresiba® (Insulin Degludec) to Evaluate Long Term Safety and Efficacy in Patients With Diabetes Mellitus in Routine Clinical Practice in India Enrolling by invitation Novo Nordisk A/S N/A This study is conducted in Asia. The aim of the study is to evaluate long term safety and efficacy of Tresiba® (insulin degludec) in patients with diabetes mellitus in routine clinical practice in India.
NCT02192450 Insulin Degludec and Symptomatic Nocturnal Hypoglycaemia Recruiting Aarhus University Hospital Phase 4 The purpose of this study is to determine whether insulin degludec compared to insulin glargine can reduce the risk of symptomatic nocturnal hypoglycaemia in subjects with the greatest potential benefit from optimised insulin treatment, which are patients with type 1 diabetes and high risk of nocturnal severe hypoglycaemia.
NCT02192450 Insulin Degludec and Symptomatic Nocturnal Hypoglycaemia Recruiting Copenhagen University Hospital, Denmark Phase 4 The purpose of this study is to determine whether insulin degludec compared to insulin glargine can reduce the risk of symptomatic nocturnal hypoglycaemia in subjects with the greatest potential benefit from optimised insulin treatment, which are patients with type 1 diabetes and high risk of nocturnal severe hypoglycaemia.
NCT02192450 Insulin Degludec and Symptomatic Nocturnal Hypoglycaemia Recruiting Hvidovre University Hospital Phase 4 The purpose of this study is to determine whether insulin degludec compared to insulin glargine can reduce the risk of symptomatic nocturnal hypoglycaemia in subjects with the greatest potential benefit from optimised insulin treatment, which are patients with type 1 diabetes and high risk of nocturnal severe hypoglycaemia.
NCT02192450 Insulin Degludec and Symptomatic Nocturnal Hypoglycaemia Recruiting Odense University Hospital Phase 4 The purpose of this study is to determine whether insulin degludec compared to insulin glargine can reduce the risk of symptomatic nocturnal hypoglycaemia in subjects with the greatest potential benefit from optimised insulin treatment, which are patients with type 1 diabetes and high risk of nocturnal severe hypoglycaemia.
NCT02192450 Insulin Degludec and Symptomatic Nocturnal Hypoglycaemia Recruiting Steno Diabetes Center Phase 4 The purpose of this study is to determine whether insulin degludec compared to insulin glargine can reduce the risk of symptomatic nocturnal hypoglycaemia in subjects with the greatest potential benefit from optimised insulin treatment, which are patients with type 1 diabetes and high risk of nocturnal severe hypoglycaemia.
Trial ID Title Status Sponsor Phase Summary

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Clinical Trial Conditions for Tresiba

Condition Name

Condition Name for Tresiba
Intervention Trials
Diabetes Mellitus, Type 2 6
Diabetes 4
Diabetes Mellitus, Type 1 4
Type 1 Diabetes Mellitus 3
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Condition MeSH

Condition MeSH for Tresiba
Intervention Trials
Diabetes Mellitus 13
Diabetes Mellitus, Type 2 9
Diabetes Mellitus, Type 1 7
Hypoglycemia 1
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Clinical Trial Locations for Tresiba

Trials by Country

Trials by Country for Tresiba
Location Trials
United States 27
Spain 4
United Kingdom 4
Italy 4
France 3
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Trials by US State

Trials by US State for Tresiba
Location Trials
Georgia 2
California 2
Arizona 1
Florida 1
Illinois 1
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Clinical Trial Progress for Tresiba

Clinical Trial Phase

Clinical Trial Phase for Tresiba
Clinical Trial Phase Trials
Phase 4 8
N/A 6
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Clinical Trial Status

Clinical Trial Status for Tresiba
Clinical Trial Phase Trials
Recruiting 4
Not yet recruiting 4
Enrolling by invitation 3
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Clinical Trial Sponsors for Tresiba

Sponsor Name

Sponsor Name for Tresiba
Sponsor Trials
Novo Nordisk A/S 7
Sanofi 3
Sydvestjysk Hospital 1
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Sponsor Type

Sponsor Type for Tresiba
Sponsor Trials
Other 15
Industry 10
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Serving hundreds of leading biopharmaceutical companies globally:

Citi
Boehringer Ingelheim
Argus Health
McKesson
Daiichi Sankyo
Farmers Insurance
Accenture
Queensland Health
Teva

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