- Trials with a EudraCT protocol (42)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
42 result(s) found for: Fructosamine.
Displaying page 1 of 3.
EudraCT Number: 2013-002172-40 | Sponsor Protocol Number: ISIS426115-CS2 | Start Date*: 2014-01-08 | |||||||||||
Sponsor Name:Isis Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, Double Blind, Placebo-Controlled, Phase 2 Study to Assess the Safety, Tolerability and Efficacy of ISIS 426115 (an Antisense Glucocorticoid Receptor Antagonist) Administered Subcutane... | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000592-17 | Sponsor Protocol Number: MODY-TREAT | Start Date*: 2012-08-03 | |||||||||||
Sponsor Name:Signe H. Østoft, Diabetes Research Division | |||||||||||||
Full Title: The effects of GLP-1 in Maturity- onset diabetes of the young (MODY) | |||||||||||||
Medical condition: 'Maturity onset diabetes of the young', also called 'Hepatocyte nuclear factor 1-alfa daiabetes'. It is a monogenic form of inherited diabetes. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016382-29 | Sponsor Protocol Number: P1736-05/34/09 | Start Date*: 2009-11-06 |
Sponsor Name:Piramal Life Sciences Limited | ||
Full Title: A Phase II, 12-Week Randomised, Double-Blind, Placebo-Controlled, Proof of Concept Study to Evaluate Safety, Tolerability, Pharmacokinetics and Effect On Glycemic Control of P1736-05 in Subjects wi... | ||
Medical condition: Diabetes mellitus, type 2 (Blood Glucose Lowering Effect)/ | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) HU (Completed) CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004959-23 | Sponsor Protocol Number: NPJ005-DM2-0521 | Start Date*: 2018-07-05 | |||||||||||
Sponsor Name:neopharma Japan Co., Ltd | |||||||||||||
Full Title: A 24-week, Phase IIa, Double blind, Randomized, Parallel Group, Placebo controlled, Exploratory Study to Evaluate the Efficacy and Safety of 5 Aminolevulinic Acid Co-administered with Sodium Ferrou... | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus in Patients who have not Achieved Adequate Glycemic Control with Maximum Tolerated Dose of Metformin Daily or Sulfonylurea | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002852-13 | Sponsor Protocol Number: BPI-CT-005 | Start Date*: 2006-11-21 |
Sponsor Name:Bexel Pharmaceuticals Inc. | ||
Full Title: Double blind, placebo-controlled dose escalating, multiple dose study with two groups of 30 volunteers with type II diabetes to assess efficacy on glucose-profile, triglycerides and blood pressure ... | ||
Medical condition: dose escalating, multiple dose study with two groups of 30 volunteers with type II diabetes | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001502-28 | Sponsor Protocol Number: PRED-AID | Start Date*: 2019-02-11 | |||||||||||
Sponsor Name:Imperial College London | |||||||||||||
Full Title: Safety and Efficacy of Prednisolone in Adrenal Insufficiency Disease (PRED-AID Study) | |||||||||||||
Medical condition: Adrenal insufficiency | |||||||||||||
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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: 2010-019665-28 | Sponsor Protocol Number: 10-HM11260C-201 | Start Date*: 2010-05-07 | |||||||||||
Sponsor Name:Hanmi Pharmaceutical Company Limited | |||||||||||||
Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, SEQUENTIAL DOSE ESCALATION STUDY OF THE SAFETY, TOLERABILITY, PHARMACODYNAMICS AND PHARMACOKINETICS OF SINGLE SUBCUTANEOUS DOSES OF HM11260C IN ADULT... | |||||||||||||
Medical condition: type 2 diabetes mellitus | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003869-17 | Sponsor Protocol Number: 0893-005 | Start Date*: 2006-09-25 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: A Multi-center, Double-Blind, Double-Dummy, Placebo-Controlled, Parallel Panel Study to Assess the Safety, Tolerability, and Glucose-Lowering Efficacy of MK-0893 in Patients With Type 2 Diabetes Me... | |||||||||||||
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: 2015-000361-31 | Sponsor Protocol Number: FIM-MET-2015-01 | Start Date*: 2015-09-07 | |||||||||||
Sponsor Name:Fundación Pública Andaluza para la Investigación de Málaga en Biomedicina y Salud (FIMABIS) | |||||||||||||
Full Title: Efficacy of metformin in gestational diabetes not controlled by diet compared to the use of insulin | |||||||||||||
Medical condition: Gestational diabetes (GD) | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004944-39 | Sponsor Protocol Number: NPJ005-DM2-0522 | Start Date*: 2018-04-27 | |||||||||||
Sponsor Name:neopharma Japan Co., Ltd | |||||||||||||
Full Title: A 24 Week, Phase IIa, Double blind, Randomized, Parallel Group, Placebo-controlled, Proof of Concept Study to Assess the Efficacy and Safety of Two Doses of 5 Aminolevulinic Acid Co-administered wi... | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) HU (Completed) PL (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000645-12 | Sponsor Protocol Number: GFT505-219-8 | Start Date*: 2019-09-03 | |||||||||||
Sponsor Name:GENFIT SA | |||||||||||||
Full Title: A Double-Blind, Placebo-Controlled, Cross-over Phase II Study to Evaluate the Effect of a 6-week Elafibranor (120mg) treatment administered once daily on hepatic lipid composition in subjects with ... | |||||||||||||
Medical condition: Subjects with Nonalcoholic Fatty Liver (NAFL) | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001765-28 | Sponsor Protocol Number: BC20750 | Start Date*: 2008-10-09 | |||||||||||
Sponsor Name:F.Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A multicenter, randomized, double-blind, placebo-controlled study to assess the efficacy, safety and tolerability of taspoglutide (RO5073031) compared to placebo in patients with type 2 diabetes me... | |||||||||||||
Medical condition: Type 2 diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003716-36 | Sponsor Protocol Number: D5670C00002 | Start Date*: 2015-03-30 | |||||||||||
Sponsor Name:MedImmune Limited, a wholly owned subsidiary of AstraZeneca | |||||||||||||
Full Title: A Phase 1/2, Randomized, Double-blind, Placebo-controlled, Multiple-ascending-dose Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of MEDI0382 in Overweight and Obese Subjects with a H... | |||||||||||||
Medical condition: Type 2 Diabetes in Overweight and Obese Patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (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: 2013-000225-30 | Sponsor Protocol Number: DMA-Clin-199-2013-001 | Start Date*: 2013-04-12 | |||||||||||
Sponsor Name:DiaMedica USA Inc. | |||||||||||||
Full Title: A DOUBLE-BLINDED, PLACEBO-CONTROLLED, SINGLE DOSE AND MULTIPLE-DOSE STUDY TO EVALUATE THE SAFETY, TOLERABILITY, PHARMACOKINETICS, PHARMACODYNAMICS AND PROOF OF CONCEPT OF DM-199 IN HEALTHY SUBJECTS... | |||||||||||||
Medical condition: Diabetes Mellitus type 2 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001140-61 | Sponsor Protocol Number: GWDM1302 | Start Date*: 2013-12-30 | |||||||||||
Sponsor Name:GW Research Ltd. | |||||||||||||
Full Title: A randomised, double blind, placebo controlled, parallel group, dose ranging study of GWP42004 as add on to metformin in the treatment of participants with Type 2 diabetes. | |||||||||||||
Medical condition: Type 2 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001445-12 | Sponsor Protocol Number: GS-US-454-6075 | Start Date*: 2022-02-25 | |||||||||||
Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
Full Title: A Phase 2, Randomized, Double-Blind, Double-Dummy, Placebo-Controlled Study Evaluating the Safety and Efficacy of Semaglutide, and the Fixed-Dose Combination of Cilofexor and Firsocostat, Alone and... | |||||||||||||
Medical condition: Nonalcoholic Steatohepatitis (NASH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000867-92 | Sponsor Protocol Number: 0431-023 | Start Date*: 2004-11-18 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind Study of MK-0431 in Patients With Type 2 Diabetes Mellitus Who Have Inadequate Glycemic Control | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) LT (Completed) DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000204-15 | Sponsor Protocol Number: 060286 | Start Date*: 2017-08-08 | |||||||||||
Sponsor Name:Professor, DMSc Tina Vilsbøll | |||||||||||||
Full Title: Glimepiride monotherapy vs. combination of glimepiride and linagliptin therapy in patients with HNF1A-diabetes | |||||||||||||
Medical condition: "Hepatocyte nuclear factor 1-alfa diabetes", also called "Maturity onset diabetes of the young type 3"'. It is a monogenic form of inherited diabetes. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000969-47 | Sponsor Protocol Number: 13702908 | Start Date*: 2014-07-04 | |||||||||||
Sponsor Name:University Hospital of Toulouse | |||||||||||||
Full Title: Clinical efficacy of coordinated boluses in type 1 diabetic patients treated with insulin pumps: a multicentric, randomised, cross over study (COBOL study). | |||||||||||||
Medical condition: type 1 diabetic patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
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