- Trials with a EudraCT protocol (168)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
168 result(s) found for: Diabetes AND Lantus (Insulin glargine) AND Insulin.
Displaying page 4 of 9.
EudraCT Number: 2020-005309-18 | Sponsor Protocol Number: NN1535-4593 | Start Date*: 2021-11-30 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A 52 week study comparing the efficacy and safety of once weekly IcoSema and daily insulin glargine 100 units/mL combined with insulin aspart, both treatment arms with or without oral anti diabetic... | |||||||||||||
Medical condition: Diabetes Mellitus, Type 2 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) HU (Completed) CZ (Completed) FR (Completed) SI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003370-13 | Sponsor Protocol Number: LPS15017 | Start Date*: 2018-10-10 | |||||||||||
Sponsor Name:Sanofi-Aventis Groupe | |||||||||||||
Full Title: A multi-center open-label parallel group randomized controlled trial to compare iGlarLixi versus premixed insulin in patients with type 2 diabetes who have failed to achieve glycemic control with b... | |||||||||||||
Medical condition: Patients with Type 2 Diabetes who have failed to achieve glycemic control with basal insulin and oral antidiabetic agents(OADs) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) AT (Completed) ES (Completed) SE (Completed) BG (Completed) GR (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004622-96 | Sponsor Protocol Number: 0431-260 | Start Date*: 2011-12-23 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. (hereafter referred to as | |||||||||||||
Full Title: A Phase III, Multicenter, Randomized, Double-Blind, Placebo- Controlled Clinical Trial to Study the Safety and Insulin-Sparing Efficacy of the Addition of Sitagliptin in Patients With Type 2 Diabet... | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) IE (Completed) LT (Completed) DK (Completed) HU (Completed) BE (Completed) GB (Completed) IT (Completed) PT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-008306-43 | Sponsor Protocol Number: NN1250-1995 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A Trial Investigating the Pharmacokinetic Properties of NN1250 in Children, Adolescents and Adults with Type 1 Diabetes | |||||||||||||
Medical condition: Type I diabetes mellitus | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005776-27 | Sponsor Protocol Number: NN1250-3579 | Start Date*: 2009-07-27 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A 52-week randomised, controlled, open label, multicentre, multinational treat-to-target trial comparing the efficacy and safety of SIBA and insulin glargine, both injected once daily in combinatio... | |||||||||||||
Medical condition: Type 2 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) FI (Completed) FR (Completed) AT (Completed) ES (Completed) DK (Completed) SI (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002399-10 | Sponsor Protocol Number: EFC13799 | Start Date*: 2015-01-08 | |||||||||||
Sponsor Name:Sanofi-aventis recherche & développement | |||||||||||||
Full Title: A Randomized, Open-label, 2-arm Parallel-group, Multicenter, 26-week Study Assessing the Safety and Efficacy of H0E901-U300 Versus Lantus in Older Patients with Type 2 Diabetes Inadequately Control... | |||||||||||||
Medical condition: Type 2 diabetes mellitus | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) HU (Completed) DE (Completed) ES (Completed) IT (Completed) GB (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003971-12 | Sponsor Protocol Number: MK-1293-003 | Start Date*: 2014-04-01 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Phase III Clinical Trial to Study the Safety and Efficacy of MK-1293 Compared to Lantus? in Subjects With Type 1 Diabetes Mellitus. | |||||||||||||
Medical condition: Type 1 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004421-28 | Sponsor Protocol Number: A2171084 | Start Date*: 2006-11-09 | |||||||||||
Sponsor Name: | |||||||||||||
Full Title: A SIX MONTH, OPEN-LABEL OUTPATIENT, RANDOMIZED PARALLEL GROUP TRIAL ASSESSING THE IMPACT OF DRY POWDER INHALED INSULIN (EXUBERA®) ON GLYCEMIC CONTROL COMPARED TO INSULIN GLARGINE (LANTUS®) IN PATIE... | |||||||||||||
Medical condition: Diabetes Mellitus type II (not insulin independent) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DE (Completed) SE (Completed) FR (Completed) BE (Completed) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012317-22 | Sponsor Protocol Number: PBBT | Start Date*: 2009-12-04 | ||||||||||||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERO UNIVERSITARIA OSPEDALI RIUNITI UMBERTO I - G.M.LANCISI - G.SALESI | ||||||||||||||||||||||||||||
Full Title: PEDIATRIC BASAL BOLUS THERAPY - Basal-Bolus regimen in the treatment of children with type 1 diabetes | ||||||||||||||||||||||||||||
Medical condition: pre-puberal children with T1DM | ||||||||||||||||||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000087-27 | Sponsor Protocol Number: NN304-1431 | Start Date*: 2004-07-04 | |||||||||||
Sponsor Name:Novo Nordisk Farma Oy | |||||||||||||
Full Title: A one-year, multi-national, open-labelled, parallel-group, 2:1 randomised treat-to-target trial comparing efficacy and safety of insulin detemir with insulin glargine using a basal-bolus regimen wi... | |||||||||||||
Medical condition: Type 2 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006860-12 | Sponsor Protocol Number: GWT-2008-1 | Start Date*: 2008-12-23 | |||||||||||
Sponsor Name:GWT-TUD GmbH | |||||||||||||
Full Title: Comparative investigation of Insuline glargine versus Metformin as first line drug in treat-ment of early Type 2 Diabetes (GLORY) | |||||||||||||
Medical condition: Diabetes mellitus Type II | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003980-21 | Sponsor Protocol Number: NN304-1724 | Start Date*: 2006-01-19 | |||||||||||
Sponsor Name:Novo Nordisk Ltd | |||||||||||||
Full Title: A Multinational, Open Label, Randomised, Three Period, Cross Over Trial Investigating The Impact Of Exercise And Type Of Basal Insulin Used On Blood Glucose Levels In Subjects With Type 1 Diabetes ... | |||||||||||||
Medical condition: Type 1 Diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006573-24 | Sponsor Protocol Number: Glargine and EPC | Start Date*: 2007-07-11 | |||||||||||
Sponsor Name:University Hospital of Heidelberg | |||||||||||||
Full Title: Prospective influence of bedtime insulin glargine on mobilization and function of endothelial progenitor cells in patients with type 2 diabetes: a partially double-blind, randomized, three-arm unic... | |||||||||||||
Medical condition: The medical disease that will be investigated is type 2, diabetes mellitus. The patients who will be investigated are between 35 and 70 years old and on oral antidiabetic therapy. | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000027-40 | Sponsor Protocol Number: PDY12625 | Start Date*: 2012-04-26 | |||||||||||
Sponsor Name:Sanofi-Aventis Recherche & Développement | |||||||||||||
Full Title: An open-label, randomized, three-parallel-group study on pharmacodynamic effects of 8-week QD treatment with lixisenatide compared to liraglutide in patients with type 2 diabetes not adequately con... | |||||||||||||
Medical condition: Type 2 Diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002957-22 | Sponsor Protocol Number: H80-MC-GWBR | Start Date*: 2008-03-13 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: Efficacy of once weekly exenatide long acting release and once daily insulin glargine in patients with Type 2 diabetes treated with metformin alone or in combination with sulphonylurea. | |||||||||||||
Medical condition: Type 2 Diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) HU (Completed) BE (Completed) DK (Completed) GR (Completed) FR (Completed) CZ (Completed) DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005774-13 | Sponsor Protocol Number: NN1250-3583 | Start Date*: 2009-07-24 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A 52 week randomised, controlled, open label, multicentre, multinational, parallel, treat-to-target trial comparing efficacy and safety of SIBA and insulin glargine both administered once daily in ... | |||||||||||||
Medical condition: type 1 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001557-29 | Sponsor Protocol Number: A2171035 | Start Date*: 2006-11-24 | |||||||||||
Sponsor Name:Pfizer Inc. | |||||||||||||
Full Title: A 52-WEEK MULTICENTER, OPEN-LABEL, RANDOMIZED, PARALLEL, TWO - ARM STUDY COMPARING EXUBERA® (INHALED HUMAN INSULIN) VS. HUMALOG® (INSULIN LISPRO), BOTH IN COMBINATION WITH INSULIN GLARGINE IN SUBJE... | |||||||||||||
Medical condition: Type 1 Diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) DE (Prematurely Ended) GB (Prematurely Ended) NL (Completed) IE (Prematurely Ended) AT (Prematurely Ended) FI (Prematurely Ended) FR (Completed) SE (Prematurely Ended) BE (Completed) PT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001930-32 | Sponsor Protocol Number: NN1250-3995 | Start Date*: 2014-08-13 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A randomised, double blind, cross-over trial comparing the safety and efficacy of insulin degludec and insulin glargine, both with insulin aspart as mealtime insulin in subjects with type 1 diabetes | |||||||||||||
Medical condition: Diabetes Mellitus, Type 1 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011271-78 | Sponsor Protocol Number: NN5401-3590 | Start Date*: 2009-10-02 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A trial comparing efficacy and safety of NN5401 with insulin glargine in insulin naive subjects with type 2 diabetes | |||||||||||||
Medical condition: type 2 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000959-15 | Sponsor Protocol Number: HOE901/4057 | Start Date*: 2005-05-17 |
Sponsor Name:sanofi-aventis | ||
Full Title: A multicenter clinical trial to evaluate quality of life in patients with Type 2 diabetes before and after changing therapy to a combination of insulin glargine and oral antidiabetic drugs in a rea... | ||
Medical condition: Patients with Type 2 diabetes inadequately controlled on a combination of highest tolerable dose of oral antidiabetic drugs (OAD) + neutral protamine hagedorn (NPH) insulin for more than 3 months | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
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