- Trials with a EudraCT protocol (2,112)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
2,112 result(s) found for: Type 2 diabetes.
Displaying page 12 of 106.
EudraCT Number: 2010-018664-16 | Sponsor Protocol Number: F3Z-MC-IOPW | Start Date*: 2010-09-09 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Double-Blind, Randomized, Crossover Trial of CSII Reservoir In-use Comparing Insulin Lispro Formulation to Insulin Aspart in Patients with Type 1 Diabetes Mellitus | |||||||||||||
Medical condition: type 1 diabetes | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) FR (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001843-74 | Sponsor Protocol Number: DRI6738 | Start Date*: 2006-11-08 | |||||||||||
Sponsor Name:Sanofi-Synthelabo Recherche | |||||||||||||
Full Title: A randomized, double-blind, parallel-group, placebo-controlled, dose-response, multicentre, multinational study evaluating the efficacy and safety of AVE2268 administered either twice daily (breakf... | |||||||||||||
Medical condition: Type 2 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) DK (Completed) BE (Completed) IT (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004674-97 | Sponsor Protocol Number: MB102-229 | Start Date*: 2015-01-15 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-controlled, Parallel Group, Phase 3 Study to Evaluate the Efficacy and Safety of Dapagliflozin as an Add-on to Insulin Therapy in Subjects with Type... | |||||||||||||
Medical condition: Type 1 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) GB (Completed) FI (Completed) IT (Completed) DE (Completed) AT (Completed) ES (Completed) HU (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002739-40 | Sponsor Protocol Number: GLP1_glucose_control | Start Date*: 2017-07-27 | |||||||||||
Sponsor Name:Radboud university medical center | |||||||||||||
Full Title: Beta cell imaging in type 1 diabetes with stable near-normal and unstable glucose control using PET | |||||||||||||
Medical condition: Type 1 diabetes | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006599-39 | Sponsor Protocol Number: VIAject™-06J | Start Date*: 2007-08-28 | |||||||||||
Sponsor Name:BIODEL Inc. | |||||||||||||
Full Title: An Open Label, Multi-Center, Randomized, Parallel Group Study Comparing the Efficacy and Safety of Insulin VIAJECT™ and Regular Human Insulin in Patients with Type 1 Diabetes Mellitus | |||||||||||||
Medical condition: Diabetes Mellitus Type 1 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003060-59 | Sponsor Protocol Number: NN304-1761 | Start Date*: 2007-03-16 | |||||||||||
Sponsor Name:Novo Nordisk Limited | |||||||||||||
Full Title: A 32 week, national, single-centre, open-labelled, randomised, cross-over trial comparing energy expenditure with insulin detemir versus NPH insulin using a basal-bolus regimen with insulin aspart ... | |||||||||||||
Medical condition: Type 1 diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002285-76 | Sponsor Protocol Number: 1111-1155-9921 | Start Date*: 2014-12-04 | |||||||||||
Sponsor Name:Hvidovre University Hospital | |||||||||||||
Full Title: The Effects of Liraglutide in Patients With Insulin Pump Treated Type 1 Diabetes: A Randomized, Placebo-Controlled Trial. The Lira Pump Trial. | |||||||||||||
Medical condition: Type 1 Diabetes | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002945-12 | Sponsor Protocol Number: EFC12619 | Start Date*: 2014-11-12 | |||||||||||
Sponsor Name:Sanofi-aventis recherche et développement | |||||||||||||
Full Title: Six-month, Randomized, Open-label, Parallel-group Comparison of SAR342434 to Humalog® in Adult Patients With Type 1 Diabetes Mellitus Also Using Insulin Glargine, with a 6-month Safety Extension Pe... | |||||||||||||
Medical condition: Type1-Diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001732-37 | Sponsor Protocol Number: TAK-875_306 | Start Date*: 2012-08-29 | |||||||||||||||||||||||||||||||
Sponsor Name:Takeda Global Research & Development Centre (Europe) Ltd. | |||||||||||||||||||||||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Evaluate Cardiovascular Outcomes of TAK-875, 50 mg in Addition to Standard of Care in Subjects with Type 2 Diabetes and... | |||||||||||||||||||||||||||||||||
Medical condition: Type 2 diabetes mellitus (T2DM) | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: HU (Prematurely Ended) CZ (Prematurely Ended) SK (Prematurely Ended) DE (Prematurely Ended) EE (Prematurely Ended) LT (Prematurely Ended) LV (Prematurely Ended) GB (Completed) IT (Prematurely Ended) BG (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-006074-28 | Sponsor Protocol Number: 0893-015 | Start Date*: 2008-02-21 | |||||||||||
Sponsor Name:Merck Sharp & Dohme (Sweden) AB | |||||||||||||
Full Title: A Phase IIa, Multicenter, Double-Blind, Randomized, Active Comparator-Controlled Clinical Trial to Study the Efficacy and Safety of MK-0893 in Combination With Sitagliptin or in Combination With Me... | |||||||||||||
Medical condition: Type II Diabetes Mellitus | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) ES (Completed) DK (Completed) DE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-003764-30 | Sponsor Protocol Number: D/P2/04/3 | Start Date*: 2004-12-13 | |||||||||||
Sponsor Name:Diamyd Therapeutics AB | |||||||||||||
Full Title: A Phase II, Randomised, Double-Blind, Placebo-controlled, Multi-centre Study to Investigate the Impact of Diamyd on the Progression of diabetes in Patients Newly Diagnosed with Type 1 Diabetes Mell... | |||||||||||||
Medical condition: Type 1 diabetes | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019161-28 | Sponsor Protocol Number: BDT-09-ADC004 | Start Date*: 2010-04-06 | |||||||||||
Sponsor Name:Becton, Dickinson and Company, BD Technologies | |||||||||||||
Full Title: A single center, open-label, randomized study examining the glycemic effects of intra-dermal vs. subcutaneous bolus dosing of insulin lispro in patients with type 1 diabetes | |||||||||||||
Medical condition: Diabetes mellitus Type I | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007176-22 | Sponsor Protocol Number: Asp-BIAsp-HI-2008 | Start Date*: 2009-04-02 | |||||||||||
Sponsor Name:Department of Medicine M, Aarhus University Hospital | |||||||||||||
Full Title: A comparison of pharmacodynamics and pharmacokinetics of Insulin Aspart, Biphasic Insulin Aspart 70 and 50 & Fast-acting Human Insulin in patients with Type 1 diabetes, A randomised, quadruple cros... | |||||||||||||
Medical condition: Patients with type 1 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001365-92 | Sponsor Protocol Number: 1 | Start Date*: 2016-10-10 | |||||||||||
Sponsor Name:Center for Diabetes Research, Gentofte Hospital | |||||||||||||
Full Title: Meal-time Administration of exenatide for Glycaemic control in type 1 diabetic Cases: A randomised, placebo-controlled trial | |||||||||||||
Medical condition: Type 1 Diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013668-38 | Sponsor Protocol Number: 1245.33 | Start Date*: 2009-11-13 | |||||||||||
Sponsor Name:Boehringer Ingelheim Limited | |||||||||||||
Full Title: A phase IIb, randomised, double-blind, placebo-controlled, parallel group, safety and efficacy study of BI 10773 (10 mg and 25 mg) administered orally, once daily over 78 weeks in type 2 diabetic p... | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) GB (Completed) PT (Completed) FR (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012816-41 | Sponsor Protocol Number: D1680L00002 | Start Date*: 2009-08-12 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A 52-Week, Randomised, Double-Blind, Active-Controlled, Multi-Centre Phase IIIb/IV Study to Evaluate the Efficacy and Tolerability of Saxagliptin Compared to Glimepiride in Elderly Patients with Ty... | |||||||||||||
Medical condition: Non-insulin dependent type 2 diabetes mellitus in elderly patients (≥ 65 years) | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) DK (Completed) FI (Completed) ES (Completed) NO (Completed) AT (Completed) FR (Completed) GR (Completed) IT (Completed) GB (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002610-21 | Sponsor Protocol Number: HOEK-02 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Academic Medical Centre | |||||||||||||
Full Title: Mechanisms of albuminuria in diabetes; reversal of injury to the glycocalyx by the ACE inhibitor lisinopril | |||||||||||||
Medical condition: Diabetes mellitus | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006084-73 | Sponsor Protocol Number: VIAjectTM-07J | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:BIODEL Inc | |||||||||||||
Full Title: An Open Label, Multi-Center, Follow-on Study Examining the Long-Term Safety and Efficacy of Insulin VIAjectTM in Subjects with Type 1 Diabetes Mellitus | |||||||||||||
Medical condition: Diabetes Mellitus Type 1 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001522-88 | Sponsor Protocol Number: NN304-1708 | Start Date*: 2005-09-07 | |||||||||||
Sponsor Name:sa Novo Nordisk Pharma nv | |||||||||||||
Full Title: A four-month open-labelled randomised multi-centre two-group parallel trial comparing administration of insulin detemir once or twice daily in a basal-bolus regimen with insulin aspart in subjects ... | |||||||||||||
Medical condition: type 1 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012923-27 | Sponsor Protocol Number: NN1250-3770 | Start Date*: 2011-12-09 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: Begin™: Flex T1. A 26-week trial investigating the dosing flexibility, efficacy and safety of NN1250 in subjects with type 1 diabetes with a 26-week extension. | |||||||||||||
Medical condition: Type 1 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) BE (Completed) DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
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