- Trials with a EudraCT protocol (33)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
33 result(s) found for: Disposition index.
Displaying page 1 of 2.
EudraCT Number: 2010-023980-17 | Sponsor Protocol Number: Metformin 3.0 | Start Date*: 2011-08-24 |
Sponsor Name:St. Antonius Hospital | ||
Full Title: An efficacy, safety and pharmacokinetic study on the short-term and long-term use of METFORMIN in obese children and adolescents | ||
Medical condition: obese children and adolescents of Caucasian descent with insulin resistance in the age of ≥ 10 and ≤ 16 years at study entry. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-000913-33 | Sponsor Protocol Number: DIAB1 | Start Date*: 2020-06-02 | |||||||||||
Sponsor Name:University of gothenburg | |||||||||||||
Full Title: Semaglutide and dapagliflozin in diabetic patients with different pathophysiology | |||||||||||||
Medical condition: Type 2 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005698-31 | Sponsor Protocol Number: 4/2005 | Start Date*: 2006-09-12 |
Sponsor Name:National Medical Center (Országos Gyógyintézeti Központ) | ||
Full Title: Efficacy of fenofibrate treatment on the insulin sensitivity and pancreas ß-cell function in obese patients with hypertriglyceridemia. | ||
Medical condition: Patients non-diabetic, obese with hypertriglyceridemia (previously untreated with fibrate). | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-001896-63 | Sponsor Protocol Number: E3810-A001-015 | Start Date*: 2016-06-27 |
Sponsor Name:Eisai Medical Research Inc. | ||
Full Title: An Ascending Bioavailability of a New Oral Suspension of E3810 | ||
Medical condition: Bioavailability/Bioequivalence | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2007-005819-25 | Sponsor Protocol Number: COV070905 | Start Date*: 2008-02-29 |
Sponsor Name:Laboratoire BAILLY-CREAT | ||
Full Title: | ||
Medical condition: ANXIETE | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-002777-68 | Sponsor Protocol Number: ROV-01 | Start Date*: 2006-07-12 | |||||||||||
Sponsor Name:Cardiff and Vale NHS Trust | |||||||||||||
Full Title: The effects of rosuvastatin therapy on glucose metabolism in non-diabetic renal transplant recipients with a focus on insulin sensitivity and pancreatic beta islet cell function | |||||||||||||
Medical condition: New-onset diabetes after transplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001304-42 | Sponsor Protocol Number: 20029 | Start Date*: 2020-08-24 | ||||||||||||||||
Sponsor Name:University of Nottingham | ||||||||||||||||||
Full Title: Efficacy of Nitric Oxide in Stroke -2 | ||||||||||||||||||
Medical condition: Hyperacute stroke - both ischaemic and haemorrhage | ||||||||||||||||||
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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: 2004-002187-22 | Sponsor Protocol Number: 001 | Start Date*: 2005-04-05 |
Sponsor Name:Ullevål University Hospital | ||
Full Title: Scandinavian Candesartan Acute Stroke Trial | ||
Medical condition: Acute stroke (ischemic or haemoragic) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) DK (Completed) BE (Completed) EE (Prematurely Ended) LT (Prematurely Ended) DE (Prematurely Ended) FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-014263-40 | Sponsor Protocol Number: MEL01 | Start Date*: 2009-12-14 |
Sponsor Name:Penwest Pharmaceuticals Co. | ||
Full Title: A Phase 2a, Double Blind, Randomized, Placebo-controlled, 28 day, Two-arm, Parallel Group Study of A0001 in Patients with the A3243G Mitochondrial DNA Point Mutation and Evidence of Impaired Mitoch... | ||
Medical condition: A3243G mitochondrial DNA point mutation and evidence of impaired mitochondrial function | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2015-001552-30 | Sponsor Protocol Number: PRED-D-TRIAL2015 | Start Date*: 2015-10-13 | |||||||||||
Sponsor Name:Steno Diabetes Center A/S | |||||||||||||
Full Title: Effect of dapagliflozin, metformin and physical activity on glucose variability, body composition and cardiovascular risk in pre-diabetes (The PRE-D Trial) - A randomised, parallel, open-label, int... | |||||||||||||
Medical condition: Pre-diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003121-42 | Sponsor Protocol Number: CHDR1635 | Start Date*: 2019-11-28 | |||||||||||
Sponsor Name:Enceladus Pharmaceuticals BV | |||||||||||||
Full Title: A Phase I-IIa, Open label, Dose Escalating Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of Intravenous Pegylated Liposomal Dexamethasone Sodium Phosphate as Monotherapy in Pa... | |||||||||||||
Medical condition: Castration resistant prostate cancer with bone metastases. | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001996-35 | Sponsor Protocol Number: GS-US-431-4566 | Start Date*: 2020-03-04 | |||||||||||
Sponsor Name:Gilead Sciences Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Double-blind, Placebo and Adalimumab-controlled Study to Evaluate the Efficacy and Safety of Filgotinib in Subjects with Active Psoriatic Arthritis Who Are Naïve to Biologic ... | |||||||||||||
Medical condition: Psoriatic Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) BE (Completed) GB (GB - no longer in EU/EEA) SK (Completed) HU (Completed) PL (Completed) BG (Completed) ES (Completed) CZ (Completed) NL (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000658-27 | Sponsor Protocol Number: D5130C05262 | Start Date*: 2006-12-12 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Randomised, Double-blind, Parallel Group, Phase 3, Efficacy and Safety Study of AZD6140 Compared with Clopidogrel for Prevention of Vascular Events in Patients with Non-ST or ST Elevation Acute C... | |||||||||||||
Medical condition: non-ST and ST elevation acute coronary syndromes (ACS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) FI (Completed) PT (Completed) HU (Completed) DE (Completed) FR (Completed) SE (Completed) AT (Completed) NL (Completed) DK (Completed) SK (Completed) BE (Completed) CZ (Completed) GR (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001049-24 | Sponsor Protocol Number: NN8022-1839 | Start Date*: 2008-12-02 | ||||||||||||||||
Sponsor Name:Novo Nordisk A/S | ||||||||||||||||||
Full Title: Effect of liraglutide on body weight in non-diabetic obese subjects or overweight subjects with comorbidities A randomised, double-blind, placebo controlled, parallel group, multi-centre, multina... | ||||||||||||||||||
Medical condition: Obesity and overweight Pre-diabetes | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IE (Completed) FI (Completed) ES (Completed) DE (Completed) DK (Completed) AT (Completed) GB (Completed) FR (Completed) IT (Completed) NL (Completed) BE (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-001220-38 | Sponsor Protocol Number: CAIN457F2208 | Start Date*: 2011-07-12 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A multicenter, 12 week, randomized, double-blind, placebo-controlled biomarker study of secukinumab (AIN457) in rheumatoid arthritis patients followed by an open label extension | |||||||||||||
Medical condition: Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) BE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003547-36 | Sponsor Protocol Number: NRL972-09/2008- (CHBC) | Start Date*: 2009-02-12 | |||||||||||
Sponsor Name:Norgine Ltd | |||||||||||||
Full Title: An open study to investigate the effects of chronic hepatitis B or C on the pharmacokinetics of cholyl-lysyl-fluorescein (NRL972) before, during and after standard treatment | |||||||||||||
Medical condition: In-vivo diagnostic marker for liver dysfunction. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000907-13 | Sponsor Protocol Number: 2007-24-001 | Start Date*: 2007-11-13 | ||||||||||||||||||||||||||
Sponsor Name:MUW, Innere Med III, Abt.für Endokrinologie & Stoffwechsel | ||||||||||||||||||||||||||||
Full Title: The impact of Rimonabant in overweight women with prior gestational diabetes | ||||||||||||||||||||||||||||
Medical condition: Rimonabant has been shown to reduce body weight and improve cardiovascular risk factors and metabolic control. Therefore we investigate in women with previous gestational diabetes and impaired glu... | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: AT (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-024320-23 | Sponsor Protocol Number: I4F-EW-CCAC | Start Date*: 2011-03-08 | |||||||||||
Sponsor Name:Chorus, Eli Lilly and Company | |||||||||||||
Full Title: A Proof-of-Concept Study of the Effects of LY2828360 in the Treatment of Patients with Osteoarthritic Knee Pain | |||||||||||||
Medical condition: Pain in osteoarthritic knee. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005405-78 | Sponsor Protocol Number: 2011430 | Start Date*: 2012-02-01 | ||||||||||||||||
Sponsor Name:Steen Bendix Haugaard | ||||||||||||||||||
Full Title: Adding liraglutide to the backbone therapy of biguanide in patients with coronary artery disease and newly diagnosed type-2 diabetes | ||||||||||||||||||
Medical condition: Patients suffering of both Type 2 diabetes mellitus and coronary artery disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015459-25 | Sponsor Protocol Number: CTKI258A2302 | Start Date*: 2010-12-01 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: An open-label, randomized, multi-center, Phase III study to compare the safety and efficacy of TKI258 versus sorafenib in patients with metastatic renal cell carcinoma after failure of anti-angioge... | |||||||||||||
Medical condition: metastatic renal cell carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) NL (Completed) BE (Completed) ES (Completed) HU (Completed) SK (Completed) IT (Completed) DE (Completed) SE (Completed) AT (Completed) GR (Completed) GB (Completed) NO (Completed) | |||||||||||||
Trial results: View results |
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