- Trials with a EudraCT protocol (44,393)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
44,393 result(s) found.
Displaying page 920 of 2,220.
| EudraCT Number: 2013-004978-95 | Sponsor Protocol Number: VildaMMC | Start Date*: 2014-03-12 |
| Sponsor Name:KULeuven | ||
| Full Title: the influence of a DPP-4 inhibitor, vildaglitpin, on hunger and the migrating motor complex in healthy volunteers | ||
| Medical condition: healthy volunteers no medical condition, drug will be studied because they are known to influence gastric motility | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-002944-25 | Sponsor Protocol Number: EuroHyp-1 | Start Date*: 2014-08-20 | |||||||||||
| Sponsor Name:Universitätsklinikum Erlangen | |||||||||||||
| Full Title: EuroHYP-1: European multicentre, randomised, phase III clinical trial of therapeutic hypothermia plus best medical treatment versus best medical treatment alone for acute ischaemic stroke | |||||||||||||
| Medical condition: Acute ischaemic stroke | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) FI (Completed) IT (Completed) IE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-000453-37 | Sponsor Protocol Number: 3179/AO/14 | Start Date*: 2014-12-16 |
| Sponsor Name:Azienda Ospedaliera di Padova | ||
| Full Title: Sequential treatment with nucleotide analogue and peg-interferon in patients with HBV-related chronic hepatitis. | ||
| Medical condition: Hepatitis B virus (HBV) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: IT (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-004249-17 | Sponsor Protocol Number: NCTU:6831 | Start Date*: 2014-02-12 |
| Sponsor Name:The Newcastle upon Tyne Hospitals NHS Foundation Trust | ||
| Full Title: A randomised, placebo controlled trial of extra-oesophageal reflux treatment in the management of upper respiratory symptoms. [TOPPITS: Trial of Proton Pump Inhibitors in Throat Symptoms] | ||
| Medical condition: Persistent throat symptom - globus, hoarseness, throat clearing, throat discomfort, choking spasms, excess mucus/postnasal drip, otherwise unexplained night time cough of choking. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-002217-31 | Sponsor Protocol Number: 2215-CL-0101 | Start Date*: 2015-07-09 | |||||||||||
| Sponsor Name:Astellas Pharma Global Development, Inc. | |||||||||||||
| Full Title: A Phase 1/2 Open-Label, Dose Escalation Study Investigating the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ASP2215 in Patients with Relapsed or Refractory Acute Myeloid Leukemia | |||||||||||||
| Medical condition: Relapsed or Refractory Acute Myeloid Leukemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) IT (Completed) FR (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-001733-86 | Sponsor Protocol Number: 1710 | Start Date*: 2014-10-15 |
| Sponsor Name:Maastricht University | ||
| Full Title: The effect of L-arginine on brown adipose tissue metabolism in South Asian and white Caucasian subjects | ||
| Medical condition: Obesity, glucose intolerance, endothelial dysfunction | ||
| Disease: | ||
| Population Age: Adults | Gender: Male | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-002324-16 | Sponsor Protocol Number: CVAY736X2202 | Start Date*: 2014-06-13 | |||||||||||
| Sponsor Name:Novartis Pharma Services AG | |||||||||||||
| Full Title: A randomized, partially blind, placebo-controlled, proof-of-concept study to assess the effect of a single infusion of VAY736 on disease activity as measured by brain MRI scans in patients with rel... | |||||||||||||
| Medical condition: relapsing-remitting multiple sclerosis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-000753-24 | Sponsor Protocol Number: DC2011LiBrain001 | Start Date*: 2011-10-13 | ||||||||||||||||
| Sponsor Name:VU University Medical Center | ||||||||||||||||||
| Full Title: Central effects of endogenous GLP-1 and the GLP-1 analog liraglutide on brain satiety and reward circuits and feeding behavior in diabetes. | ||||||||||||||||||
| Medical condition: diabetes mellitus obesity | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2011-001863-39 | Sponsor Protocol Number: ML27837 | Start Date*: 2011-07-28 | |||||||||||
| Sponsor Name:Roche Austria GmbH | |||||||||||||
| Full Title: A multi-center study of the safety and effect on disease activity of Tocilizumab (TCZ) in combination with Methotrexate (MTX) versus Tocilizumab monotheraphy in patients with mild to moderate rheum... | |||||||||||||
| Medical condition: Mild to moderate rheumatoid arthritis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) | |||||||||||||
| Trial results: Removed from public view | |||||||||||||
| EudraCT Number: 2014-001836-12 | Sponsor Protocol Number: ITMC0414 | Start Date*: 2014-07-31 |
| Sponsor Name:Institute of Tropical Medicine | ||
| Full Title: Boostability for rabies in last-minute travelers: One Day Rabies Pre-exposure Intradermal Vaccination followed by one day Postexposure Intradermal Vaccination | ||
| Medical condition: Rabies is a viral infection that affects the central nervous system. It causes encephalitis which is almost invariably fatal. Preventive vaccination alone implies no complete protection, but simpli... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-001231-36 | Sponsor Protocol Number: CV185-267(B0661025) | Start Date*: 2014-08-22 | |||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
| Full Title: A phase IV trial to assess the effectiveness of Apixaban compared with usual care anticoagulation in subjects with non-valvular Atrial Fibrillation undergoing cardioversion | |||||||||||||
| Medical condition: Non-Valvular Atrial Fibrillation in patients undergoing Cardioversion | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) ES (Completed) BE (Completed) SE (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-005013-23 | Sponsor Protocol Number: M37P2E1 | Start Date*: 2014-11-25 |
| Sponsor Name:Novartis Vaccines and Diagnostics | ||
| Full Title: A Phase III Open Label, Multi-Center Pediatric Study in China Comparing a Booster Dose of Vaxem™ Hib to HIBERIX® | ||
| Medical condition: Meningitis, epiglottitis, pneumonia, arthritis caused by Haemophilus influenzae type b. | ||
| Disease: | ||
| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2013-004298-28 | Sponsor Protocol Number: MEA117106 | Start Date*: 2014-05-02 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
| Full Title: Study MEA117106: Mepolizumab vs. Placebo as add-on treatment for frequently exacerbating COPD patients. | |||||||||||||
| Medical condition: Treatment of severe Chronic Obstructive Pulmonary Disease (COPD) in patients presenting frequent exacerbations | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) CZ (Completed) PL (Completed) IT (Completed) BE (Completed) ES (Completed) EE (Completed) GR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-001062-15 | Sponsor Protocol Number: BAY59-7939/16320 | Start Date*: 2013-06-13 | ||||||||||||||||
| Sponsor Name:Bayer HealthCare AG | ||||||||||||||||||
| Full Title: An open-label, international, multicenter, interventional study exploring the efficacy of once-daily oral rivaroxaban (BAY 59-7939) for the treatment of left atrial/left atrial appendage thrombus i... | ||||||||||||||||||
| Medical condition: Atrial Fibrillation | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) BG (Completed) PL (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2012-005525-75 | Sponsor Protocol Number: SSAT052 | Start Date*: 2013-07-16 |
| Sponsor Name:St Stephen's AIDS Trust | ||
| Full Title: An open label, randomised, pilot trial of pegylated interferon, ribavirin and telaprevir versus pegylated interferon and ribavirin alone in the response guided treatment of acute hepatitis C genoty... | ||
| Medical condition: Acute hepatitis C infection | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-004411-53 | Sponsor Protocol Number: Erythromycin_v5 | Start Date*: 2014-05-15 |
| Sponsor Name:University of Leuven | ||
| Full Title: Brain mechanisms underlying the effect of the motilin receptor agonist erythromycin on hunger in normal weight subjects | ||
| Medical condition: The effect of erythromycin administration on hunger and brain responses will be tested in healthy volunteers | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-002529-30 | Sponsor Protocol Number: KER-001 | Start Date*: 2012-11-26 | |||||||||||
| Sponsor Name:Dolorgiet GmbH & Co. KG | |||||||||||||
| Full Title: Three-armed, randomized, double-blind dose-finding trial on efficiency and safety of Ibuprofen 5% gel, Ibuprofen 7,5% gel und Ibuprofen 10% gel in patients with actinic keratosis Olsen grade I/II | |||||||||||||
| Medical condition: Actinic keratosis Olsen grade I/II | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: Removed from public view | |||||||||||||
| EudraCT Number: 2014-000838-39 | Sponsor Protocol Number: GEINO14-01 | Start Date*: 2014-07-07 |
| Sponsor Name:GEINO | ||
| Full Title: Clinical Trial Phase IIB randomized, multicenter, of continuation or non-continuation with 6 cycles of temozolomide after the first 6 cycles of standard first-line treatment in patients with gliobl... | ||
| Medical condition: Patients diagnosed of Glioblastoma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-000482-36 | Sponsor Protocol Number: LUM001-201 | Start Date*: 2013-07-08 | |||||||||||
| Sponsor Name:Lumena Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A PHASE 2, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO EVALUATE LUM001, AN APICAL SODIUM-DEPENDENT BILE ACID TRANSPORTER INHIBITOR (ASBTi), IN COMBINATION WITH URSODEOXYCHOLIC ACID (UDCA)... | |||||||||||||
| Medical condition: Primary biliary cirrhosis (PBC) is a chronic and slowly progressive cholestatic liver disease of autoimmune etiology characterized by injury of the intrahepatic bile ducts that may eventually lead ... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-005532-23 | Sponsor Protocol Number: CO-1686-019 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Clovis Oncology, Inc. | |||||||||||||
| Full Title: TIGER-2: A Phase 2, Open-Label, Multicenter, Safety and Efficacy Study of Oral CO 1686 as 2nd Line EGFR-Directed TKI in Patients with Mutant EGFR Non-Small Cell Lung Cancer (NSCLC) | |||||||||||||
| Medical condition: Previously treated NSCLC patients who have documented evidence of an activating mutation in the EGFR gene and have failed treatment with an EGFR inhibitor | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) ES (Completed) NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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