- Trials with a EudraCT protocol (322)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (6)
322 result(s) found for: human insulin.
Displaying page 5 of 17.
EudraCT Number: 2012-002839-28 | Sponsor Protocol Number: NN9535-3744 | Start Date*: 2012-12-18 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A long-term, randomised, double-blind, placebo-controlled, multinational, multi-centre trial to evaluate cardiovascular and other long-term outcomes with semaglutide in subjects with type 2 diabetes | |||||||||||||
Medical condition: Diabetes Mellitus, Type 2 | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) BG (Completed) DE (Completed) DK (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003088-36 | Sponsor Protocol Number: GPPAD-03-POInT | Start Date*: 2018-01-30 | |||||||||||
Sponsor Name:Technische Universität München, Represented by the school of medicine | |||||||||||||
Full Title: GPPAD-POInT (Global Platform of Autoimmune Diabetes – Primary Oral Insulin Trial) Oral Insulin Therapy for Prevention of Autoimmune Diabetes | |||||||||||||
Medical condition: risk for type 1 diabetes | |||||||||||||
|
|||||||||||||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) GB (GB - no longer in EU/EEA) PL (Completed) DE (Completed) BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005768-15 | Sponsor Protocol Number: NN5401-3592 | Start Date*: 2009-06-23 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A 26-week, randomised, open-labelled, two-arm, parallel-group, treat-to-target trial comparing efficacy and safety of soluble insulin analogue combination (SIAC) twice daily (BID) with biphasic ins... | |||||||||||||
Medical condition: type 2 diabetes | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006550-96 | Sponsor Protocol Number: TN-07 | Start Date*: 2007-03-23 | |||||||||||
Sponsor Name:NIDDK TYPE 1 DIABETES TRIALNET | |||||||||||||
Full Title: Oral insulin for prevention of diabetes in relatives at risk for type 1 diabetes mellitus | |||||||||||||
Medical condition: prevention of type 1 diabetes mellitus in subjects at risk for T1DM | |||||||||||||
|
|||||||||||||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) FI (Completed) DE (Completed) GB (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002778-50 | Sponsor Protocol Number: BIAsp-1440 | Start Date*: 2005-03-02 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A multi-national, open labelled, randomised, stratified, parallel group 36 week comparison of twice daily Biphasic Insulin Aspart 30 versus thrice daily Biphasic Insulin Aspart 50 and 70 all in com... | |||||||||||||
Medical condition: Type 2 diabetes | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) DK (Completed) HU (Completed) GB (Completed) CZ (Completed) IT (Completed) BE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007945-29 | Sponsor Protocol Number: BALAD | Start Date*: 2009-09-25 | |||||||||||
Sponsor Name:Institute of Cancer research and molecular medicine. | |||||||||||||
Full Title: Treatment of LADA . | |||||||||||||
Medical condition: Latent Autoimmune diabetes of the adult (LADA) is a form of diabetes where the onset of the diabetes starts after 30 years of age, there is presence of beta-cell directed antibodies (mostly anti-GA... | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) FI (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004731-29 | Sponsor Protocol Number: NN1998-1617 | Start Date*: 2007-06-07 | |||||||||||||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||||||||||||
Full Title: Inhaled preprandial human insulin with the AERx® iDMS versus subcutaneous injected insulin aspart in subjects with diabetes and chronic obstructive pulmonary disease: A 52-week, open-label, multice... | |||||||||||||||||||||||
Medical condition: Type 1 Diabetes Type 2 Diabetes COPD | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: SK (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-001527-11 | Sponsor Protocol Number: Protocol H7U-MC-IDAS | Start Date*: 2005-08-17 |
Sponsor Name:Eli Lilly and Company | ||
Full Title: A Pivotal, Open-Label, Parallel Study to Evaluate the Safety and Efficacy of Human Insulin Inhalation Powder (HIIP) Compared to Injectable Insulin in Patients With Diabetes and COPD or Asthma | ||
Medical condition: Patients with type 1 diabetes mellitus and many patients with type 2 diabetes mellitus require daily use of insulin for the maintenance of normal glucose homeostasis. At present, insulin can be de... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2011-003733-34 | Sponsor Protocol Number: APIDR_L_05719 | Start Date*: 2011-09-13 | |||||||||||
Sponsor Name:ikfe – Institute for Clinical Research and Development | |||||||||||||
Full Title: Human Insulin Analogs: Evaluation of inflammatory mRNA expression of Macrophages and Endothelial function of Short-acting insulin – HERMES Pilot Study | |||||||||||||
Medical condition: Patients with Diabetes mellitus Type 2 and a stable basal supported oral therapy | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004489-15 | Sponsor Protocol Number: MKC-TI-118 | Start Date*: 2007-12-27 | |||||||||||
Sponsor Name:MannKind Corporation | |||||||||||||
Full Title: Comparison of Technosphere®/Insulin, Insulin Lispro and Exubera® Effect on Endogenous Glucose Production After a Meal Challenge and During a Euglycemic Glucose Clamp Procedure in Subjects with Typ... | |||||||||||||
Medical condition: Type 2 diabetes mellitus. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005381-37 | Sponsor Protocol Number: H7U-MC-IDAW | Start Date*: 2006-06-19 |
Sponsor Name:Eli Lilly and Company Ltd | ||
Full Title: A Phase 3, Open-Label, Parallel Group Treatment Concordance Study to Compare Insulin Use and Its Effect on Glycemic Control in Patients with Type 2 Diabetes Mellitus: Two Populations with Differen... | ||
Medical condition: Male or female non smoking adults (18-100 years old), diagnosed type 2 Diabetes Mellitus for at least 6 months duration at study entry. Taking at least one or more oral anti-hyperglycemic medicatio... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-004622-81 | Sponsor Protocol Number: NN1998-1616 | Start Date*: 2007-11-02 | |||||||||||||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||||||||||||
Full Title: Inhaled preprandial human insulin with the AERx® iDMS versus subcutaneous injected insulin aspart in subjects with diabetes and asthma: a 52-week, open-label, multinational, randomised, parallel tr... | |||||||||||||||||||||||
Medical condition: Type 1 diabetes Type 2 diabetes Asthma | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: SK (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) | |||||||||||||
|
|||||||||||||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005583-10 | Sponsor Protocol Number: NN1218-4049 | Start Date*: 2013-05-15 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: Efficacy and safety of FIAsp in a basal-bolus regimen versus basal insulin therapy, both in combination with metformin in adult Subjects with type 2 diabetes | |||||||||||||
Medical condition: Diabetes Mellitus, Type 2 | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005051-15 | Sponsor Protocol Number: 0431-051 | Start Date*: 2007-01-15 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: A Phase III, Multicenter, Randomized, Double-Blind Clinical Trial to Study the Safety and Efficacy of the Addition of Sitagliptin (MK-0431) to Patients with Type 2 Diabetes Mellitus Who Have Inade... | |||||||||||||
Medical condition: type II Diabetes mellitus | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) IE (Completed) DK (Completed) FI (Completed) BE (Completed) FR (Completed) PT (Completed) AT (Prematurely Ended) IT (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002457-69 | Sponsor Protocol Number: CP-MGA031-01 | Start Date*: 2008-12-04 | |||||||||||
Sponsor Name:MacroGenics, Inc. | |||||||||||||
Full Title: A Phase 2/3, Randomized, Double-Blind, Multicenter, Multinational, 4-Arm, Controlled, Dose-Ranging Study to Evaluate Efficacy and Safety of Teplizumab (MGA031), a Humanized, FcR Non-Binding, Anti-C... | |||||||||||||
Medical condition: Recent-onset type I diabetes mellitus (T1DM) | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) SE (Completed) GB (Completed) EE (Completed) NL (Completed) LV (Completed) ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002999-17 | Sponsor Protocol Number: H7U-MC-IDAY | Start Date*: 2006-09-18 | |||||||||||
Sponsor Name:Eli Lilly and Company Limited | |||||||||||||
Full Title: A Phase 3, Open-Label, Parallel-Group Study to Compare Two Dosing Algorithms for Preprandial Human Insulin Inhalation Powder (HIIP) in Insulin-Naïve Patients with Type 2 Diabetes Mellitus | |||||||||||||
Medical condition: Male or non pregnant female nonsmoking patients, 18 years of age or older: have had type 2 diabetes mellitus for at least 6 months, and have been treated with one or more oral antihyperglycemic med... | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) BE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001590-29 | Sponsor Protocol Number: 022007 | Start Date*: 2007-07-06 | |||||||||||
Sponsor Name:Herz-, Thorax- und Gefäßchirurgische Anästhesie und Intensivmedizin | |||||||||||||
Full Title: Insulin aspart (NovoRapid®, Novo Nordisk) vs. human insulin (Actrapid®, Novo Nordisk) in intravenous treatment of high blood glucose concentrations in the ICU | |||||||||||||
Medical condition: Therapy of hyperglycemia by intravenously applied insulin is going to be investigated. Hyperglycemia is very common in hospitalized, critically ill patients, even if they have not previously had di... | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004137-42 | Sponsor Protocol Number: 0431-066 | Start Date*: 2007-10-28 | |||||||||||
Sponsor Name:Merck Sharp & Dohme GmbH | |||||||||||||
Full Title: A Phase III Randomized, Active-Comparator (Pioglitazone) Controlled Clinical Trial to Study the Efficacy and Safety of MK-0431A (A Fixed-Dose Combination Tablet of Sitagliptin and Metformin) in Pat... | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) IE (Completed) HU (Completed) SE (Completed) SI (Completed) GB (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 | |||||||||||||
|
|||||||||||||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
