- Trials with a EudraCT protocol (914)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
914 result(s) found for: Metformin.
Displaying page 45 of 46.
| EudraCT Number: 2020-005309-18 | Sponsor Protocol Number: NN1535-4593 | Start Date*: 2021-11-30 | |||||||||||
| Sponsor Name:Novo Nordisk A/S | |||||||||||||
| Full Title: A 52 week study comparing the efficacy and safety of once weekly IcoSema and daily insulin glargine 100 units/mL combined with insulin aspart, both treatment arms with or without oral anti diabetic... | |||||||||||||
| Medical condition: Diabetes Mellitus, Type 2 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) IT (Completed) HU (Completed) CZ (Completed) FR (Completed) SI (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-002121-36 | Sponsor Protocol Number: 0941-007 | Start Date*: 2008-07-11 | |||||||||||
| Sponsor Name:MSD Finland Oy | |||||||||||||
| Full Title: A Phase IIb/III, Multicenter, Randomized, Double-Blind, Placebo-Controlled Dose- Range Finding Clinical Trial of MK-0941 in Patients With Type 2 Diabetes Mellitus With Inadequate Glycemic Control o... | |||||||||||||
| Medical condition: Treatment of Type 2 Diabetes | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) SE (Completed) AT (Prematurely Ended) DK (Prematurely Ended) FR (Prematurely Ended) IT (Prematurely Ended) DE (Prematurely Ended) HU (Completed) BG (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-017004-91 | Sponsor Protocol Number: 1218.56 | Start Date*: 2011-03-31 | |||||||||||
| Sponsor Name:Boehringer Ingelheim France | |||||||||||||
| Full Title: A randomised, double-blind, placebo-controlled parallel group dose finding study of linagliptin (1 mg or 5 mg administered orally once daily) over 12 weeks in children and adolescents, from 10 to 1... | |||||||||||||
| Medical condition: Patients with type 2 diabetes. | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) PL (Completed) IT (Completed) Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-005121-24 | Sponsor Protocol Number: NN9838-4609 | Start Date*: 2022-07-26 | |||||||||||||||||||||
| Sponsor Name:Novo Nordisk A/S | |||||||||||||||||||||||
| Full Title: Efficacy and safety of cagrilintide s.c. 2.4 mg in combination with semaglutide s.c. 2.4 mg (CagriSema s.c. 2.4 mg/2.4 mg) once-weekly in participants withoverweight or obesityand type 2 diabetes | |||||||||||||||||||||||
| Medical condition: Overweight, Obesity and Diabetes Mellitus, Type 2 | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: HU (Trial now transitioned) PL (Trial now transitioned) IE (Trial now transitioned) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2021-005057-87 | Sponsor Protocol Number: 337HNAS21016 | Start Date*: 2022-06-15 | |||||||||||
| Sponsor Name:Inventiva S.A. | |||||||||||||
| Full Title: A placebo-controlled, proof-of-concept study to evaluate the safety and efficacy of Lanifibranor alone and in combination with the sodium-glucose transport protein 2 (SGLT2) inhibitor EmpaGliflozin... | |||||||||||||
| Medical condition: Type 2 Diabetes (T2DM) with Non-Alcoholic Steatohepatitis (NASH) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) BE (Completed) NL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-003107-29 | Sponsor Protocol Number: N°005 | Start Date*: 2015-08-07 | |||||||||||
| Sponsor Name:GALMED Pharmaceuticals LTD. | |||||||||||||
| Full Title: A Phase IIb, double blind, randomized controlled clinical trial to evaluate the efficacy and safety of two Aramchol doses versus placebo in patients with Non-Alcoholic- Steatohepatitis (NASH). | |||||||||||||
| Medical condition: Non-alcoholic Steatohepatitis in patients with two additional features of metabolic syndrome -overweight or obesity and Diabetes Mellitus type II or pre-diabetes. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) RO (Ongoing) LT (Completed) IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-002157-79 | Sponsor Protocol Number: DPB107246 | Start Date*: 2006-10-11 | |||||||||||
| Sponsor Name:GlaxoSmithKline | |||||||||||||
| Full Title: “A Multi-Center, Double-Blind, Parallel-Group, Randomized, Placebo-Controlled Study to Evaluate the Efficacy, Safety, and Tolerability of Denagliptin in Subjects With Type 2 Diabetes Mellitus” | |||||||||||||
| Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-002422-78 | Sponsor Protocol Number: 1 | Start Date*: 2013-10-14 | |||||||||||
| Sponsor Name:University of Leicester | |||||||||||||
| Full Title: Impact of liraglutide on cardiac function and structure in young adults with type 2 diabetes: an open lable, randomised active-comparator trial. | |||||||||||||
| Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (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: 2014-000988-41 | Sponsor Protocol Number: UoL000977 | Start Date*: 2014-08-22 | ||||||||||||||||
| Sponsor Name:University of Liverpool | ||||||||||||||||||
| Full Title: A randomized, controlled multi-centre trial of 26 weeks of subcutaneous Liraglutide (a GLP1 receptor agonist), with or without continuous positive airway pressure (CPAP), in patients with Type 2 Di... | ||||||||||||||||||
| Medical condition: Obstructive Sleep Apnoea and Type 2 Diabetes | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2013-005395-18 | Sponsor Protocol Number: U1111-1144-0576 | Start Date*: 2015-02-06 | ||||||||||||||||
| Sponsor Name:University Medical Center Utrecht | ||||||||||||||||||
| Full Title: Effects of GLP1 agonist liraglutide in patients with antipsychotic-drugs-associated diabetes mellitus | ||||||||||||||||||
| Medical condition: antipsychotic-drugs-associated diabetes mellitus | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2017-003197-13 | Sponsor Protocol Number: ISIS484137-CS2 | Start Date*: 2017-11-24 | ||||||||||||||||
| Sponsor Name:Ionis Pharmaceuticals, Inc. | ||||||||||||||||||
| Full Title: A Double-Blind, Randomized, Placebo-Controlled, Phase 2 Study to Evaluate the Safety, Tolerability and Pharmacodynamics of ISIS 484137 (ISIS-DGAT2RX, an Antisense Inhibitor of Diacylglycerol Acyltr... | ||||||||||||||||||
| Medical condition: Hepatic Steatosis in type 2 diabetes (T2DM) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: HU (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2016-002179-91 | Sponsor Protocol Number: MLE4901-101 | Start Date*: 2017-01-17 | |||||||||||
| Sponsor Name:Millendo Therapeutics, Inc. | |||||||||||||
| Full Title: A Double-blind, Randomized, Parallel-group, Placebo-controlled Study of MLE4901 for the Treatment of Polycystic Ovary Syndrome (PCOS) | |||||||||||||
| Medical condition: Polycystic Ovary Syndrome | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-019724-30 | Sponsor Protocol Number: F3Z-CR-IOQE | Start Date*: 2010-12-17 | |||||||||||
| Sponsor Name:Lilly S.A. | |||||||||||||
| Full Title: Comparación de insulina lispro premezclada (proporción baja) dos veces al día frente a insulina glargina una vez al día e insulina lispro prandial una vez al día, como estrategias de intensificació... | |||||||||||||
| Medical condition: Diabetes tipo 2 | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-000305-35 | Sponsor Protocol Number: MKC-T1-102 | Start Date*: 2006-06-23 | |||||||||||
| Sponsor Name:MannKind Corporation | |||||||||||||
| Full Title: A Prospective, Multi-Center, Open-Label, Randomized, Controlled Clinical Trial Comparing the Efficacy and Safety in Subjects With Type 2 Diabetes Receiving Subcutaneous Basal Insulin and Prandial I... | |||||||||||||
| Medical condition: Diabetes mellitus type II | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) ES (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-014958-16 | Sponsor Protocol Number: I2Q-MC-GMAH | Start Date*: 2010-01-15 | |||||||||||
| Sponsor Name:Lilly S.A. | |||||||||||||
| Full Title: A 12-Week, Phase 2, Randomized, Double-Blind, Placebo-Controlled Study of LY2599506 in Patients with Type 2 Diabetes Mellitus Treated with Diet and Exercise, with or without Metformin Estudio de fa... | |||||||||||||
| Medical condition: diabetes mellitus tipo 2 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-000825-38 | Sponsor Protocol Number: M16-04EMPA-EYE | Start Date*: 2016-10-20 | |||||||||||
| Sponsor Name:Hannover Medical School | |||||||||||||
| Full Title: SGLT2-inhibition with Empagliflozin reduces progression of diabetic retinopathy in patients with high risk of diabetic macular edema (The SUPER-Trial) | |||||||||||||
| Medical condition: Patients with type 2 diabetes mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-000217-32 | Sponsor Protocol Number: VK2809-202 | Start Date*: 2021-02-16 | ||||||||||||||||
| Sponsor Name:VIKING THERAPEUTICS, INC. | ||||||||||||||||||
| Full Title: VK2809 A PHASE 2B, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTICENTER STUDY TO ASSESS THE EFFICACY, SAFETY, AND TOLERABILITY OF VK2809 ADMINISTERED FOR 52 WEEKS FOLLOWED BY A 4-WEEK OFF-DRUG... | ||||||||||||||||||
| Medical condition: non-alcoholic steatohepatitis with fibrosis | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2019-002977-69 | Sponsor Protocol Number: BEYOND | Start Date*: 2019-11-14 | ||||||||||||||||
| Sponsor Name:A.O.U. Università degli Studi della Campania "Luigi Vanvitelli" | ||||||||||||||||||
| Full Title: Durability of combination of insulin and GLP-1 receptor agonist or SGLT-2 inhibitors versus basal bolus insulin regimen in type 2 diabetes: a randomized controlled trial | ||||||||||||||||||
| Medical condition: Type 2 diabetes mellitus | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2015-005593-38 | Sponsor Protocol Number: NN9924-4257 | Start Date*: 2016-09-09 | |||||||||||
| Sponsor Name:Novo Nordisk A/S | |||||||||||||
| Full Title: Efficacy and Safety of Oral Semaglutide Using a Flexible Dose Adjustment Based on Clinical Evaluation versus Sitagliptin in Subjects with Type 2 Diabetes Mellitus. A 52 week Randomised, Open-label,... | |||||||||||||
| Medical condition: Diabetes Mellitus, Type 2 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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