- Trials with a EudraCT protocol (926)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
926 result(s) found for: Insulin-Dependent Diabetes Mellitus 1.
Displaying page 1 of 47.
EudraCT Number: 2013-000007-17 | Sponsor Protocol Number: TAK-875_309 | Start Date*: 2013-06-05 | |||||||||||||||||||||||||||||||
Sponsor Name:Takeda Global Research & Development Centre (Europe) Ltd. | |||||||||||||||||||||||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled, 24-Week Study to Evaluate the Efficacy and Safety of Daily Oral TAK-875 50mg Compared With Placebo as an Add-On to Glimepiride ... | |||||||||||||||||||||||||||||||||
Medical condition: Type 2 diabetes mellitus (T2DM) | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: SK (Prematurely Ended) HU (Prematurely Ended) BG (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||||||||||||||||||||||
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: 2009-011672-29 | Sponsor Protocol Number: NN1250-3585 | Start Date*: 2009-11-25 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A trial investigating the efficacy and safety of NN1250 compared to insulin detemir in subjects with type 1 diabetes mellitus in a basal/bolus treatment regimen | |||||||||||||
Medical condition: type 1 diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) IT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001752-10 | Sponsor Protocol Number: TAK-875_302 | Start Date*: 2012-10-30 | |||||||||||||||||||||||||||||||
Sponsor Name:Takeda Global Research & Development Centre (Europe) Ltd. | |||||||||||||||||||||||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo- and Active-Controlled, Phase 3 Study to Evaluate the Efficacy and Safety of TAK-875 25 mg and 50 mg Compared to Placebo and Sitagliptin 100 mg When... | |||||||||||||||||||||||||||||||||
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) BG (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-002741-35 | Sponsor Protocol Number: TAK-875_301 | Start Date*: 2012-02-15 | ||||||||||||||||||||||||||
Sponsor Name:Takeda Global Research & Development Centre (Europe) Ltd. | ||||||||||||||||||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Evaluate the Efficacy and Safety of Daily Oral TAK-875 25 mg and 50 mg Compared with Placebo in Subjects with Type 2 Diabetes | ||||||||||||||||||||||||||||
Medical condition: Type 2 diabetes mellitus (T2DM) | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: SK (Completed) HU (Completed) BG (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-001291-19 | Sponsor Protocol Number: BC3-CT-002 | Start Date*: 2011-05-20 | ||||||||||||||||
Sponsor Name:Adocia SA | ||||||||||||||||||
Full Title: A phase IIa, double-blinded, randomized trial comparing the pharmacokinetics, pharmacodynamics and safety of BioChaperone® rhInsulin to fast-acting insulin analog in patients with Type 1 Diabetes m... | ||||||||||||||||||
Medical condition: Diabetes mellitus | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-001039-72 | Sponsor Protocol Number: RP06 | Start Date*: 2008-03-06 | ||||||||||||||||
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust, jointly with University of Cambridge | ||||||||||||||||||
Full Title: Adolescent Type 1 Diabetes Cardio-Renal Intervention Trial | ||||||||||||||||||
Medical condition: Type 1 diabetes in adolescents | ||||||||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-005846-35 | Sponsor Protocol Number: UF 7878 | Start Date*: 2007-02-07 | |||||||||||
Sponsor Name:Centre Hospitalier Universitaire de Montpellier Direction Recherche, Qu | |||||||||||||
Full Title: COMPARISON OF TWO KINETICS OF ADMINISTRATION OF BOLUS BY INSULIN PORTABLE PUMP ON THE GLUCOSE BLOOD STABILITY FOR INSULIN-DEPENDENT PATIENTS | |||||||||||||
Medical condition: INSULIN-DEPENDENT PATIENTS USING AN INSULIN PORTABLE PUMP | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001227-45 | Sponsor Protocol Number: PHT/2017/20 | Start Date*: 2017-06-12 | |||||||||||||||||||||
Sponsor Name:Portsmouth Hospitals NHS Trust | |||||||||||||||||||||||
Full Title: Comparison of ambulatory glucose profile prior to and during pancreatic enzyme replacement therapy in patients with diabetes and pancreatic exocrine insufficiency: a single-arm phase IV trial | |||||||||||||||||||||||
Medical condition: Type 1 diabetes and type 2 diabetes mellitus Pancreatic exocrine insufficiency | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-001222-27 | Sponsor Protocol Number: EU-IIT-006 | Start Date*: 2007-11-06 | |||||||||||||||||||||
Sponsor Name:Imperial College London | |||||||||||||||||||||||
Full Title: The effect of Pioglitazone on vascular and ventricular function in people with type 2 diabetes PICCOLA | |||||||||||||||||||||||
Medical condition: Diabetes | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-002949-35 | Sponsor Protocol Number: NN1250-1988 | Start Date*: 2011-11-01 | ||||||||||||||||
Sponsor Name:Novo Nordisk A/S | ||||||||||||||||||
Full Title: This trial is a randomized, single-centre, double-blind, two-period cross-over glucose clamp trial to test for bioequivalence between two SIBA (IDeg) formulations in healthy subjects. This trial... | ||||||||||||||||||
Medical condition: Healthy volunteers (Diabetes Mellitus, Type 1 and Diabetes Mellitus, Type 2) | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: Outside EU/EEA | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-003808-35 | Sponsor Protocol Number: CL2-44497-004 | Start Date*: 2007-11-13 | |||||||||||
Sponsor Name:Servier Research and Development Ltd. | |||||||||||||
Full Title: Dose ranging study of S 44497 administered orally once daily for four weeks in type 2 diabetic patients. A multicentre, randomised, double-blind, double-dummy, phase II study versus placebo and gli... | |||||||||||||
Medical condition: Type 2 Diabetes | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007805-58 | Sponsor Protocol Number: KP-MSD-01-08 | Start Date*: 2009-11-16 | ||||||||||||||||||||||||||
Sponsor Name:Med. Klinik II, Grosshadern, Klinikum der Universität München | ||||||||||||||||||||||||||||
Full Title: The effect of sitagliptin on postprandial lipoprotein metabolism in patients with diabetes mellitus type 2 | ||||||||||||||||||||||||||||
Medical condition: Diabetes mellitus type 2 | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-008296-33 | Sponsor Protocol Number: 1218.36 | Start Date*: 2009-06-29 | ||||||||||||||||||||||||||
Sponsor Name:Boehringer Ingelheim Finland Ky | ||||||||||||||||||||||||||||
Full Title: A Phase III randomised, double-blind, placebo-controlled, parallel group efficacy and safety study of Linagliptin (5 mg), administered orally once daily for at least 52 weeks in type 2 diabetic pa... | ||||||||||||||||||||||||||||
Medical condition: Type 2 diabetes pretreated with basal Insulin therapy | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FI (Completed) DE (Completed) NL (Completed) ES (Completed) SK (Completed) BE (Completed) CZ (Completed) IT (Completed) SE (Completed) GR (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-002267-15 | Sponsor Protocol Number: GluST1_vers4_2014 | Start Date*: 2014-07-31 | |||||||||||
Sponsor Name:Hvidovre Hospital | |||||||||||||
Full Title: Treatment of hypoglycemia with glucagon among patients with type 1 diabetes mellitus | |||||||||||||
Medical condition: Patients with type 1 diabetes mellitus | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000322-11 | Sponsor Protocol Number: HEPPI-02 | Start Date*: 2015-03-23 | |||||||||||
Sponsor Name:Medizinische Universität Graz; Universitätsklinik für Innere Medizin; Abteilung für Endokrinologie und Stoffwechsel | |||||||||||||
Full Title: Assessment of the Duration of Glucagon’s Waning Effect on the Hepatic Glucose Production in Type 1 Diabetes Patients | |||||||||||||
Medical condition: Diabetes mellitus type 1 | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005311-32 | Sponsor Protocol Number: RHEO-01 | Start Date*: 2016-01-21 | |||||||||||
Sponsor Name:Medizinische Universität Graz; Universitätsklinik fürInnere Medizin; Abteilung für Endokrinologie und Stoffwechsel | |||||||||||||
Full Title: Assessment of the Hydraulic Tissue Resistance at the Site of Subcutaneous Insulin Infusion in Patients with Type 1 Diabetes | |||||||||||||
Medical condition: Diabetes Mellitus type 1 | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
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: 2015-002342-30 | Sponsor Protocol Number: CINFONY-01 | Start Date*: 2015-07-14 | |||||||||||
Sponsor Name:Medizinische Universität Graz; Universitätsklinik für InnereMedizin; Abteilung für Endokrinologie und Stoffwechsel | |||||||||||||
Full Title: Combining Glucagon and Insulin Infusion with Glucose Sensing in Subcutaneous Adipose Tissue of Type 1 Diabetes Patients | |||||||||||||
Medical condition: Diabetes Mellitus type 1 | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000019-27 | Sponsor Protocol Number: 0431-049 | Start Date*: 2007-03-14 | |||||||||||
Sponsor Name:Merck & Co., Inc | |||||||||||||
Full Title: A Multicenter, Double-Blind, Randomized Study to Evaluate the Safety and Efficacy of Sitagliptin Compared With Metformin in Patients With Type 2 Diabetes Mellitus With Inadequate Glycemic Control | |||||||||||||
Medical condition: type II diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) FI (Completed) IE (Completed) HU (Completed) DK (Completed) ES (Completed) GB (Completed) AT (Completed) GR (Completed) DE (Completed) EE (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
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