- Trials with a EudraCT protocol (32)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
32 result(s) found for: Juvenile Onset Diabetes Mellitus AND Diabetes AND Diabetes Standard of Care Treatment.
Displaying page 1 of 2.
| 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: 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: View results | |||||||||||||
| EudraCT Number: 2015-004843-38 | Sponsor Protocol Number: LPS14585 | Start Date*: 2016-01-20 | |||||||||||
| Sponsor Name:Sanofi-Aventis Groupe | |||||||||||||
| Full Title: A Randomized, Double-blind, 2x2 Cross-over Euglycemic Clamp Study in Two Parallel Cohorts to Compare the Pharmacodynamic and Pharmacokinetic Properties of 0.4 and 0.6 U/kg/day Insulin Glargine (Tou... | |||||||||||||
| Medical condition: Type1 Diabetes Mellitus | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| 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: 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: 2009-011606-41 | Sponsor Protocol Number: CP-MGA031-03 | Start Date*: 2009-09-15 | |||||||||||
| Sponsor Name:MacroGenics, Inc. | |||||||||||||
| Full Title: A Phase 3, Randomized, Double-Blind, Multinational, Placebo-Controlled Study to Evaluate Efficacy and Safety of Teplizumab (MGA031), a Humanized, FcR Non-Binding, Anti-CD3 Monoclonal Antibody, in C... | |||||||||||||
| Medical condition: Recent-onset type 1 diabetes mellitus | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) NL (Prematurely Ended) ES (Completed) FI (Completed) GB (Completed) DE (Completed) BE (Completed) PL (Completed) FR (Completed) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-021259-22 | Sponsor Protocol Number: TRX4_DM_008_WW_10 | Start Date*: 2010-12-15 | |||||||||||
| Sponsor Name:TolerX, Inc. | |||||||||||||
| Full Title: DEFEND-1 Long Term Follow Up: Durable-Response Therapy Evaluation for Early or New Onset Type 1 Diabetes Extension Study | |||||||||||||
| Medical condition: Otelixizumab iis being developed for the treatment of patients with autoimmune T1DM with residual beta cell function (RBCF), for the purpose of preserving RBCF in this patient population. Currently... | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Prematurely Ended) SE (Prematurely Ended) DE (Prematurely Ended) ES (Prematurely Ended) DK (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-003968-20 | Sponsor Protocol Number: MEX0114 | Start Date*: 2015-10-08 | |||||||||||||||||||||||||||||||
| Sponsor Name:Dompé farmaceutici s.p.a. | |||||||||||||||||||||||||||||||||
| Full Title: A phase 2, multicentre, randomized, double-blind, placebo-controlled study to assess the efficacy and safety of 400 mg twice a day oral ladarixin in patients with new-onset type 1 diabetes | |||||||||||||||||||||||||||||||||
| Medical condition: new onset type 1 diabetes | |||||||||||||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: IT (Completed) DE (Completed) BE (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2008-008432-82 | Sponsor Protocol Number: CP-MGA031-02 | Start Date*: 2009-07-01 | |||||||||||
| Sponsor Name:MacroGenics, Inc. | |||||||||||||
| Full Title: A Multicenter, Multinational Extension of Study CP-MGA031-01 to Evaluate the Long-Term Efficacy and Safety of Teplizumab (MGA031), a Humanized, FcR Non-Binding, Anti-CD3 Monoclonal Antibody, in Chi... | |||||||||||||
| Medical condition: Recent-onset type 1 diabetes mellitus | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Prematurely Ended) ES (Prematurely Ended) SE (Prematurely Ended) LV (Prematurely Ended) EE (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-004353-40 | Sponsor Protocol Number: MYL-1501D-3003 | Start Date*: 2016-02-02 | |||||||||||
| Sponsor Name:Mylan GmbH | |||||||||||||
| Full Title: AN OPEN-LABEL, RANDOMIZED, MULTI-CENTER, PARALLEL-GROUP CLINICAL TRIAL COMPARING THE EFFICACY AND SAFETY OF MYLAN’S INSULIN GLARGINE WITH LANTUS® IN TYPE 1 DIABETES MELLITUS PATIENTS: AN EXTENSI... | |||||||||||||
| Medical condition: Type 1 Diabetes Mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) SK (Completed) LV (Completed) HU (Completed) EE (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-020166-20 | Sponsor Protocol Number: CACZ885I2208 | Start Date*: 2011-01-06 | |||||||||||
| Sponsor Name:Novartis Pharma Services AG | |||||||||||||
| Full Title: A randomized, double-blind, multiple-dose, placebo-controlled, parallel group study to evaluate the safety, tolerability, immunogenicity, pharmacokinetics, and pharmacodynamics of ACZ885 in patient... | |||||||||||||
| Medical condition: Type-1 diabetes mellitus | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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: 2009-013090-18 | Sponsor Protocol Number: NN2211-3619 | Start Date*: 2012-02-10 | |||||||||||
| Sponsor Name:Novo Nordisk A/S | |||||||||||||
| Full Title: A 52-Week Randomised, Double-Blind, Placebo-Controlled, Parallel-Group, Multi-Center, Multinational Exploratory Trial In Islet Cell Transplant Subjects With Type 1 Diabetes Mellitus To Evaluate The... | |||||||||||||
| Medical condition: Diabetes Mellitus, Type 1 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-004120-11 | Sponsor Protocol Number: GN17DI706 | Start Date*: 2020-05-05 | |||||||||||
| Sponsor Name:NHS Greater Glasgow and Clyde [...] | |||||||||||||
| Full Title: Triple Therapy for Type 1 Diabetes with Insulin, Semaglutide and Dapagliflozin | |||||||||||||
| Medical condition: Type 1 diabetes | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-004354-25 | Sponsor Protocol Number: 1245.78 | Start Date*: 2013-10-29 | |||||||||||
| Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
| Full Title: A 28-day randomised, placebo-controlled, double-blind parallel group phase IIa trial to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of once daily oral doses of 2.5 mg, 10... | |||||||||||||
| Medical condition: Diabetes mellitus type 1 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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: 2020-003916-28 | Sponsor Protocol Number: PRIFEN01 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Warszawski Uniwersytet Medyczny | |||||||||||||
| Full Title: Randomized, double-blind, multicenter, parallel group, placebo-controlled study to evaluate the efficacy and safety of phenofibrate treatment on the functions of beta cells in children and adolesce... | |||||||||||||
| Medical condition: Evaluation of the effect of phenofibrate on the functions of beta cells in children with new diagnosis of type 1 diabetes | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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: 2014-002522-12 | Sponsor Protocol Number: P121001 | Start Date*: 2014-12-10 | |||||||||||
| Sponsor Name:Assistance Publique - Hôpitaux de Paris (AP-HP) | |||||||||||||
| Full Title: European phase-II clinical trial evaluating efficacy of low dose rhIL-2 in patients with recently diagnosed type 1 diabetes | |||||||||||||
| Medical condition: type -I diabetes | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) NL (Completed) SE (Completed) DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-002966-15 | Sponsor Protocol Number: LDX0419 | Start Date*: 2021-02-22 | |||||||||||
| Sponsor Name:Dompe farmaceutici s.p.a. | |||||||||||||
| Full Title: A phase 2, multicenter, randomized, double-blind, placebo-controlled study to assess the efficacy and safety of 400 mg twice a day oral ladarixin in patients with new-onset type 1 diabetes and pres... | |||||||||||||
| Medical condition: New-onset Type 1 Diabetes | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) IT (Completed) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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