- Trials with a EudraCT protocol (926)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
926 result(s) found for: Diabetes Mellitus, Insulin-Dependent, 1.
Displaying page 17 of 47.
EudraCT Number: 2014-005028-92 | Sponsor Protocol Number: BC3-CT011 | Start Date*: 2015-01-06 | |||||||||||
Sponsor Name:Adocia | |||||||||||||
Full Title: Blood glucose control with BC222 insulin lispro compared to insulin lispro (Humalog®) after ingestion of a standardised meal. | |||||||||||||
Medical condition: Diabetes mellitus type 1 | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003732-12 | Sponsor Protocol Number: AMG109 | Start Date*: 2015-09-18 | |||||||||||
Sponsor Name:Locemia Solutions ULC | |||||||||||||
Full Title: A multiple center, open label, prospective, observational study to evaluate the effectiveness and ease-of-use of AMG504-1 administered in the home or school environments for treating hypoglycemia i... | |||||||||||||
Medical condition: Type 1 diabetes | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000189-13 | Sponsor Protocol Number: CNTO148DML2001 | Start Date*: 2021-01-14 | |||||||||||
Sponsor Name:Janssen Biologics BV | |||||||||||||
Full Title: SIMPONI® to Arrest β-cell Loss in Type 1 Diabetes | |||||||||||||
Medical condition: SIMPONI® to Arrest β-cell Loss in Type 1 Diabetes | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005287-41 | Sponsor Protocol Number: ZP4207-15126 | Start Date*: 2016-01-20 | |||||||||||
Sponsor Name:Zealand Pharma A/S | |||||||||||||
Full Title: A randomized, double-blind trial of single doses of ZP4207 administered s.c. to hypoglycemic Type 1 diabetic patients to describe the pharmacokinetics and pharmacodynamics of ZP4207 as compared to ... | |||||||||||||
Medical condition: Type 1 Diabetes mellitus | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000854-11 | Sponsor Protocol Number: H80-MC-GWCH | Start Date*: 2008-09-26 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: Safety and Efficacy of Exenatide Once Weekly Injection versus Metformin, Dipeptidyl Peptidase-4 Inhibitor, or Thiazolidinedione as Monotherapy in Drug-Naive Patients with Type 2 Diabetes | |||||||||||||
Medical condition: Type 2 Diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) PL (Completed) SK (Completed) ES (Completed) FR (Completed) DE (Completed) IT (Completed) BE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004520-42 | Sponsor Protocol Number: WJMSC-01 | Start Date*: 2021-03-24 | |||||||||||
Sponsor Name:Uppsala University Hospital | |||||||||||||
Full Title: “A Double-blinded, Randomized, Parallel, Placebo-controlled trial of Wharton´s Jelly-derived Allogeneic Mesenchymal Stromal Cells to treat Type I Diabetes in Children and Adolescents” | |||||||||||||
Medical condition: Type I diabetes | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017228-24 | Sponsor Protocol Number: CMM/DM1 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Instituto Científico y Tecnológico de Navarra | |||||||||||||
Full Title: Ensayo clínico de tratamiento de la Diabetes Mellitus tipo 1 autoinmune con células madre mesenquimales autólogas | |||||||||||||
Medical condition: Diatetes mellitus tipo 1 autoinmune | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-002356-39 | Sponsor Protocol Number: D/P2/22/8 | Start Date*: 2022-12-14 | |||||||||||
Sponsor Name:Diamyd Medical AB | |||||||||||||
Full Title: DiaPrecise, A Phase II Open Label Study to evaluate the safety and feasibility of intralymphatic administration of Diamyd® in individuals at risk for Type 1 diabetes carrying the HLA DR3-DQ2 haplotype | |||||||||||||
Medical condition: Stage 1 or stage 2 pre-type1 diabetes (seropositive for two or more T1D–associated autoantibodies) | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001158-23 | Sponsor Protocol Number: U1111-1243-4058 | Start Date*: 2023-06-01 | |||||||||||
Sponsor Name:Steno Diabetes Center Copenhagen | |||||||||||||
Full Title: Fast-Acting Insulin Aspart and Insulin Pump Settings: “THE FAST PUMP SETTING STUDY” | |||||||||||||
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: 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: 2014-001323-76 | Sponsor Protocol Number: EDCR_IIa | Start Date*: 2014-11-20 | |||||||||||
Sponsor Name:Linköping University | |||||||||||||
Full Title: Open Label trial to evaluate the tolerability of a combination therapy consisting of GAD-alum (Diamyd®), etanercept and vitamin D in children and adolescents newly diagnosed with type 1 diabetes | |||||||||||||
Medical condition: Newly diagnosed Type 1 diabetes (within 100 days) | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001713-39 | Sponsor Protocol Number: TCD601F201 | Start Date*: 2022-11-28 | |||||||||||
Sponsor Name:ITB-MED AB | |||||||||||||
Full Title: A 12-month, randomized, single-blind, placebo-controlled exposure-response study of TCD601 (siplizumab) in new onset type 1 diabetes patients (STRIDE) | |||||||||||||
Medical condition: New onset Type I Diabetes | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001926-71 | Sponsor Protocol Number: LDX0319 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Dompe farmaceutici s.p.a. | |||||||||||||
Full Title: A phase 2, multicenter, randomized, double-blind, placebo-controlled study to assess the effect and safety of 400 mg twice a day oral ladarixin in patients with recent onset type 1 diabetes and a l... | |||||||||||||
Medical condition: Recent onset Type 1 Diabetes | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) SI (Completed) BE (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004553-25 | Sponsor Protocol Number: CCFZ533X2207 | Start Date*: 2019-09-25 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: Investigator- and subject-blinded, randomized, placebo-controlled study to evaluate safety, tolerability, pharmacokinetics and efficacy of CFZ533 in pediatric and young adults with new onset type 1... | |||||||||||||
Medical condition: Treatment of subjects with type 1 diabetes mellitus with residual beta cell function (RBCF), with the goal of preserving RBCF | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) SI (Completed) DE (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023198-21 | Sponsor Protocol Number: STH15295 | Start Date*: 2011-05-25 | |||||||||||
Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | |||||||||||||
Full Title: The Relative Effectiveness of Pumps Over MDI and Structured Education. | |||||||||||||
Medical condition: Type-1 Diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005256-26 | Sponsor Protocol Number: 1245.72 | Start Date*: 2015-12-23 | |||||||||||
Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
Full Title: A Phase III, randomised, double blind, placebo-controlled, parallel group, efficacy, safety and tolerability trial of once daily, oral doses of empagliflozin as adjunctive to insulin therapy over 2... | |||||||||||||
Medical condition: Patients with confirmed, insulin-dependent type 1 diabetes mellitus for at least 1 year | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SE (Completed) GB (Completed) FI (Completed) IE (Completed) LV (Completed) NL (Completed) HU (Completed) PT (Completed) GR (Completed) FR (Completed) CZ (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005220-33 | Sponsor Protocol Number: D1690C00004 | Start Date*: 2008-02-08 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A 52-Week, International, Multi-centre, Randomised, Parallel-group, Double-blind, Active-controlled, Phase III study with a 156-Week Extension Period to Evaluate the Efficacy and Safety of Dapaglif... | |||||||||||||
Medical condition: Type 2 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) SE (Completed) DE (Completed) FR (Completed) NL (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006715-77 | Sponsor Protocol Number: NN304-1813 | Start Date*: 2007-07-12 | |||||||||||
Sponsor Name:Novo Nordisk Pharmaceutique S.A.S. | |||||||||||||
Full Title: A randomised, multicentric, open labelled, parallel group trial with insulin aspart and insulin detemir, investigating the glycaemic effect and profile in children with Type 1 diabetes, of two se... | |||||||||||||
Medical condition: Investigating the glycaemic effect and profile in children with Type 1 diabetes | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004951-12 | Sponsor Protocol Number: D1680C00007 | Start Date*: 2008-02-05 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Short-term 12-Week, Multi-centre, Randomized, Parallel-group, Double-blind, Placebo-controlled Study to Evaluate the Treatment Effect of Saxagliptin compared with Placebo in Adult Patients with T... | |||||||||||||
Medical condition: Type 2 diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) LT (Completed) HU (Completed) CZ (Completed) EE (Completed) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003998-55 | Sponsor Protocol Number: D1680C00001 | Start Date*: 2007-11-27 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A 52-Week International, Multi-centre, Randomised, Parallel-group, Double-blind, Active-controlled, Phase III study with a 52-Week Extension Period to Evaluate the Safety and Efficacy of Saxaglipti... | |||||||||||||
Medical condition: Type 2 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) NL (Completed) HU (Completed) SK (Completed) DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
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