- Trials with a EudraCT protocol (2,112)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
2,112 result(s) found for: Type 2 diabetes.
Displaying page 9 of 106.
EudraCT Number: 2008-005263-34 | Sponsor Protocol Number: MMB003 | Start Date*: 2009-01-14 | |||||||||||
Sponsor Name:The Mater Foundation/HRB Grant | |||||||||||||
Full Title: The effect of insulin therapy on beta-cell survival in patients with Maturity Onset Diabetes of the Young ( MODY) 3. A 2 year, single-centre, open-label, randomised, parallel-group trial comparing... | |||||||||||||
Medical condition: The effect of insulin therapy on beta-cell survival in patients with Maturity Onset Diabetes of the Young ( MODY ) 3. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-005136-41 | Sponsor Protocol Number: FIM-DAPA-2018-01 | Start Date*: 2018-12-12 | |||||||||||
Sponsor Name:Fundación Pública Andaluza para la Investigación de Málaga en Biomedicina Y Salud (FIMABIS) | |||||||||||||
Full Title: SGLT-2 Inhibition and Cardiovascular Disease. Metabolomics Study of Potential Factors Involved in Cardioprotection | |||||||||||||
Medical condition: Type 2 Diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011399-31 | Sponsor Protocol Number: NN1250-3718 | Start Date*: 2009-12-21 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: BEGIN™: EASY PM A trial comparing the efficacy and safety of NN1250 and insulin glargine in subjects with type 2 diabetes | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) HU (Completed) FR (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002159-16 | Sponsor Protocol Number: 0431-024 | Start Date*: 2004-11-03 | |||||||||||
Sponsor Name:Suomen MSD Oy | |||||||||||||
Full Title: A Multicenter, Double-Blind, Randomized Study to Evaluate the Safety and Efficacy of the Addition of MK-0431 Compared With Sulfonylurea Therapy in Patients With Type 2 Diabetes With Inadequate Glyc... | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) SE (Completed) DK (Completed) AT (Completed) LT (Completed) HU (Completed) CZ (Completed) GB (Completed) IT (Completed) DE (Completed) BE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018318-62 | Sponsor Protocol Number: 0431-229 | Start Date*: 2010-06-01 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: A Phase III, Randomized, Clinical Trial to Evaluate the Safety and Efficacy of the Addition of Sitagliptin in Patients With Type 2 Diabetes Mellitus Who Have Inadequate Glycemic Control on a Sulfon... | |||||||||||||
Medical condition: Diabetes Mellitus type 2 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006092-21 | Sponsor Protocol Number: NN2211-1797 | Start Date*: 2007-05-14 | |||||||||||
Sponsor Name:Novo Nordisk a/s | |||||||||||||
Full Title: Effect on glycaemic control of liraglutide or exenatide added to metformin, sulphonylurea or a combination of both in subjects with type 2 diabetes A 26-week randomised, open-label, active compara... | |||||||||||||
Medical condition: type 2 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) IE (Completed) FI (Completed) DE (Completed) ES (Completed) DK (Completed) SI (Completed) FR (Completed) PL (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000886-35 | Sponsor Protocol Number: TAK-875_203 | Start Date*: 2013-12-04 | |||||||||||||||||||||||||||||||
Sponsor Name:Takeda Development Centre Europe Ltd. | |||||||||||||||||||||||||||||||||
Full Title: A Phase 2 Randomized, Placebo-Controlled, Double-Blind Parallel-Group, Multicenter Study to Evaluate the Glycemic Effects and Safety of Fasiglifam 25 mg Twice Daily and 50 mg Once Daily on Glycemic... | |||||||||||||||||||||||||||||||||
Medical condition: Type 2 diabetes mellitus (T2DM) | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: SK (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-005979-97 | Sponsor Protocol Number: 0816202 | Start Date*: 2009-01-27 | |||||||||||
Sponsor Name:CHU de Toulouse | |||||||||||||
Full Title: EFFICACITE DU TRAITEMENT PAR POMPE A INSULINE EXTERNE CHEZ LE DIABETIQUE DE TYPE 2 : ETUDE RANDOMISEE EN PARALLELE SUR 1 AN VERSUS MULTI-INJECTIONS | |||||||||||||
Medical condition: diabète de type II | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023433-35 | Sponsor Protocol Number: 2010.639 | Start Date*: 2011-06-01 | |||||||||||
Sponsor Name:Hospices Civils de Lyon | |||||||||||||
Full Title: Implication des radicaux libres produits par la xanthine oxydase dans les altérations mitochondriales du muscle squelettique de patients diabétiques | |||||||||||||
Medical condition: diabète type 2 | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003666-85 | Sponsor Protocol Number: 11418 | Start Date*: 2015-12-03 | |||||||||||
Sponsor Name:Oxford University Hospitals NHS Trust | |||||||||||||
Full Title: Investigation of appropriate timing of additional insulin dosing for fat and protein in children with type 1 diabetes using multiple daily injections | |||||||||||||
Medical condition: Type 1 diabetes | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004434-41 | Sponsor Protocol Number: 70917 | Start Date*: 2020-04-16 | |||||||||||
Sponsor Name:Flemming Pociot | |||||||||||||
Full Title: Fenofibrate as an Early Treatment Option in Type 1 Diabetes: A randomized, double-blind, placebo-controlled, trial to evaluate antidiabetic effects of Fenofibrate in patient with newly onset type 1... | |||||||||||||
Medical condition: Newly onset Type 1 Diabetes, with first insulin injection maximum six weeks prior inclusion in this trial | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007334-22 | Sponsor Protocol Number: EFC10780 | Start Date*: 2009-11-02 | |||||||||||
Sponsor Name:Sanofi-Aventis Recherche & Développement | |||||||||||||
Full Title: A randomized, double-blind, double-dummy, 2-arm parallel-group, multicenter 24-week study comparing the efficacy and safety of AVE0010 to sitagliptin as add-on to metformin in obese type 2 diabetic... | |||||||||||||
Medical condition: Type II Diabetes | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001692-19 | Sponsor Protocol Number: NN304-1633 | Start Date*: 2005-02-25 | |||||||||||
Sponsor Name:Novo Nordisk AS | |||||||||||||
Full Title: A single-centre, randomised, double-blind, cross-over trial comparing the within-subject variability of the pharmacokinetic profiles of insulin detemir and insulin glargine in children and adolesce... | |||||||||||||
Medical condition: Type I Diabetes | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000743-68 | Sponsor Protocol Number: LDX0122 | Start Date*: 2022-12-13 | |||||||||||
Sponsor Name:DOMPé FARMACEUTICI S.P.A. | |||||||||||||
Full Title: A phase II randomized, placebo-controlled, double-blinded, 2-parallel arm, clinical trial evaluating Ladarixin 400 mg twice a day as adjunctive therapy to improve glycemic control in overweight ins... | |||||||||||||
Medical condition: overweight insulin-resistant patients with type 1 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003760-38 | Sponsor Protocol Number: E7001-H001 | Start Date*: 2005-10-14 | |||||||||||
Sponsor Name:Sten Madsbad | |||||||||||||
Full Title: Effect of three doses of nasal glp-1 versus placebo on postprandial hyperglycaemia in type 2 diabetes. | |||||||||||||
Medical condition: postprandial hyperglycaemia in type 2 diabetes | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002104-32 | Sponsor Protocol Number: NN1218-3888 | Start Date*: 2014-11-14 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A trial investigating the pharmacokinetic properties of FIAsp in children, adolescents and adults with type 1 diabetes | |||||||||||||
Medical condition: Diabetes Mellitus, Type 1 | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-004993-68 | Sponsor Protocol Number: 85256 | Start Date*: 2022-04-28 | |||||||||||
Sponsor Name:Steno Diabetes Center Copenhagen | |||||||||||||
Full Title: The HYPO-AVOID STUDY: Low-dose Glucagon and Advanced Hybrid Closed-loop System for Prevention of Exercise-Induced Hypoglycaemia in People with Type 1 Diabetes | |||||||||||||
Medical condition: 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: 2006-001392-37 | Sponsor Protocol Number: 0431-053 | Start Date*: 2006-07-21 | |||||||||||
Sponsor Name:Merck Sharp & Dohme GesmbH | |||||||||||||
Full Title: A Multicenter, Double-Blind, Randomized Study to Evaluate the Safety and Efficacy of the Addition of Sitagliptin to Patients With Type 2 Diabetes Mellitus Who Have Inadequate Glycemic Control on Me... | |||||||||||||
Medical condition: type 2 diabetes mellitus | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001634-28 | Sponsor Protocol Number: CVMD-DU-087 | Start Date*: 2008-11-11 | |||||||||||
Sponsor Name:University of Dundee | |||||||||||||
Full Title: Identification of genetic and functional biomarkers that predict PPAR-gamma-associated fluid retention and oedema | |||||||||||||
Medical condition: Patients with Type 2 diabetes mellitus (T2DM) whoa re not receiving insulin treatment | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000641-54 | Sponsor Protocol Number: 1245.10 | Start Date*: 2008-08-28 | |||||||||||
Sponsor Name:Boehringer Ingelheim Finland Ky | |||||||||||||
Full Title: A Phase II, randomized, parallel group safety, efficacy, and pharmacokinetics study of BI 10773 (1mg, 5mg, 10mg, 25mg, and 50mg) administered orally once daily over 12 weeks compared double blind t... | |||||||||||||
Medical condition: Typr 2 diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) FR (Completed) ES (Completed) DE (Completed) LV (Completed) AT (Completed) SK (Completed) CZ (Completed) HU (Completed) EE (Completed) | |||||||||||||
Trial results: View results |
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