- Trials with a EudraCT protocol (31,638)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (16,520)
31,638 result(s) found for: 0.
Displaying page 1,171 of 1,582.
EudraCT Number: 2011-005784-24 | Sponsor Protocol Number: MEIXO-VALV-001 | Start Date*: 2012-06-14 |
Sponsor Name:Andres Iñiguez Romo | ||
Full Title: Dual antiplatelet therapy versus oral anticoagulation for a short time to prevent cerebral embolism after percutaneous aortic valve implantation. Multicenter randomized clinical trial. | ||
Medical condition: Evaluate the efficacy of dual antiplatelet therapy versus oral anticoagulation for primary prevention of cerebral thromboembolism at three months after percutaneous aortic valve implantation (TAVI). | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-000281-23 | Sponsor Protocol Number: Oxford University(None) | Start Date*: 2009-09-10 | ||||||||||||||||
Sponsor Name:University of Oxford | ||||||||||||||||||
Full Title: Melatonin in Acute Mania Investigation (MIAMI-UK) | ||||||||||||||||||
Medical condition: Bipolar Disorder (mania and hypomania) | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-001151-39 | Sponsor Protocol Number: A1501081 | Start Date*: 2012-03-06 |
Sponsor Name:Pfizer Inc. 235 East 42nd Street, New York, NY 10017 | ||
Full Title: An Open Label, Intravenous to Oral Switch, Multiple Dose Study to Evaluate the Pharmacokinetics, Safety and Tolerability of Voriconazole in Immunocompromised Adolescents Aged 12 to <17 Years who ar... | ||
Medical condition: Invasive fungal infections | ||
Disease: | ||
Population Age: Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2012-001171-37 | Sponsor Protocol Number: 20021626 | Start Date*: 2012-03-07 |
Sponsor Name:Amgen, Inc. One Amgen Center Drive Thousand Oaks, California 91320 | ||
Full Title: A Phase IV Registry of Etanercept in Children With Juvenile Rheumatoid Arthritis | ||
Medical condition: Juvenile idiopathic arthritis (JIA) | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2011-002363-15 | Sponsor Protocol Number: ML27901 | Start Date*: 2011-08-17 | |||||||||||
Sponsor Name:Roche a/s | |||||||||||||
Full Title: Multicenter, randomized, parallel group study to compare the incidence of Tocilizumab related infusion reactions in patients with moderate to severe active RA, when infusion is given over 31 minute... | |||||||||||||
Medical condition: Adult Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IS (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002081-20 | Sponsor Protocol Number: 2010_52 | Start Date*: 2013-05-13 |
Sponsor Name:CENTRE HOSPITALIER UNIVERSITAIRE DE LILLE | ||
Full Title: A Multicenter Open label Phase II study of Pomalidomide and Dexamethasone in Progressive Relapsed or Refractory Multiple Myeloma patients with deletion 17p or translocation (4;14) Adverse Karyotypi... | ||
Medical condition: This study will determine the efficacy and toxicity profile of pomalidomide and dexamethasone in patients with adverse prognostic factors as determined using adverse karyotypic abnormalities and th... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-000933-37 | Sponsor Protocol Number: CRT113890 | Start Date*: 2012-09-18 |
Sponsor Name:National and Kapodostrian University of Athens | ||
Full Title: Phase II trial of ofatumumab combined with ESHAP as salvage therapy before autologous stem cell transplantation, for patients with relapsed or refractory diffuse large B cell lymphoma (DLBCL) previ... | ||
Medical condition: Relapsed or refractory diffuse large B cell lymphoma (DLBCL). | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-003602-25 | Sponsor Protocol Number: CBEZ235B2203 | Start Date*: 2011-12-13 | |||||||||||
Sponsor Name:Novartis Farmaceutica S.A. | |||||||||||||
Full Title: Estudio fase Ib/fase II aleatorizado, de BEZ235 y trastuzumab frente a lapatinib y capecitabina, en pacientes con cáncer de mama metastásico o localmente avanzado HER2 positivo, que no han respondi... | |||||||||||||
Medical condition: Adult female patients with HER2 positive locally advanced or metastatic breast cancer who received prior trastuzumab treatment. Phase II: patients must have additionally received prior taxane thera... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006250-90 | Sponsor Protocol Number: EARL-2 | Start Date*: 2012-07-11 |
Sponsor Name:EANM Forschungs GmbH / EANM Research Ltd. | ||
Full Title: Randomized double-blind placebo controlled Phase II study to evaluate the efficacy and safety of Sorafenib treatment in patients with advanced (recurrent, persistent and/or metastasizing) medullary... | ||
Medical condition: Advanced (recurrent, persistent and/or metastasizing) medullary thyroid carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) AT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2010-020112-11 | Sponsor Protocol Number: P07037 | Start Date*: 2011-06-29 | |||||||||||
Sponsor Name:Schering-Plough Research Institute, a division of Schering Corporation | |||||||||||||
Full Title: A Phase 3, 12-Week, Double-Blind, Placebo-Controlled Efficacy and Safety Study of Preladenant in Subjects with Moderate to Severe Parkinson’s Disease. (Phase 3; Protocol No. P07037) | |||||||||||||
Medical condition: Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005350-39 | Sponsor Protocol Number: 20122011 | Start Date*: 2013-04-22 |
Sponsor Name:University Medical Centre Groningen | ||
Full Title: Effects Of extra-fine particle HFA-becLomethasone (HFA-QVAR) Versus course particle treatment In smokers and ex-smokers with Asthma | ||
Medical condition: Asthma | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005384-24 | Sponsor Protocol Number: AM-101-CL-10-02 | Start Date*: 2012-02-06 | |||||||||||
Sponsor Name:Auris Medical AG | |||||||||||||
Full Title: TACTT1 | |||||||||||||
Medical condition: Acute inner ear tinnitus following acute acustic trauma, acute otitis media, middle ear surgery, or inner ear barotrauma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004543-12 | Sponsor Protocol Number: V70P6 | Start Date*: 2014-11-04 |
Sponsor Name:Novartis Vaccines and Diagnostics Srl. | ||
Full Title: A Phase II, Observer-Blind, Randomized, Multi-center Study to Evaluate the Safety and Immunogenicity of Two 0.25 mL or 0.5 mL Doses of Fluad® and Fluzone® Influenza Vaccines in Healthy Children Age... | ||
Medical condition: Influenza | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2015-003055-22 | Sponsor Protocol Number: AOL2015-04 | Start Date*: 2016-05-09 |
Sponsor Name:Centre Hospitalier Universitaire de Reims | ||
Full Title: Intérêt de la curarisation lors de la chirurgie laparoscopique et recherche de facteurs associés à une compliance abdominale diminuée. | ||
Medical condition: patients pris en charge pour une chirurgie intra-péritonéale programmée par laparoscopie | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-004397-96 | Sponsor Protocol Number: CF20112018 | Start Date*: 2019-04-09 | |||||||||||
Sponsor Name:Merete Hædersdal | |||||||||||||
Full Title: Impact of thermo-mechanical intervention on Protoporphyrin IX accumulation and biodistribution in normal skin following topical 5-aminolevulinic acid at high and low vehicle viscosity | |||||||||||||
Medical condition: Healthy skin on the upper back on 3 participants in study a and 12 participants in study b. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003686-26 | Sponsor Protocol Number: M16-300 | Start Date*: 2017-08-28 | |||||||||||
Sponsor Name:AbbVie Stemcentrx LLC | |||||||||||||
Full Title: A Phase 1/2 Study on the Safety of Rovalpituzumab Tesirine Administered in Combination with Nivolumab or Nivolumab and Ipilimumab for Adults with Extensive-Stage Small Cell Lung Cancer | |||||||||||||
Medical condition: Extensive-Stage Small Cell Lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002698-39 | Sponsor Protocol Number: CB8025-21528 | Start Date*: 2015-11-11 | |||||||||||
Sponsor Name:CymaBay Therapeutics Inc. | |||||||||||||
Full Title: A 12-week, double-blind, randomized, placebo-controlled, Phase 2 study to evaluate the effects of two doses of MBX-8025 in subjects with Primary Biliary Cirrhosis (PBC) and an inadequate response t... | |||||||||||||
Medical condition: Primary Biliary Cirrhosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000043-31 | Sponsor Protocol Number: 383 | Start Date*: 2020-03-26 |
Sponsor Name:Groupe Hospitalier Paris Saint-Joseph | ||
Full Title: Efficacy and tolerance of Liraglutide for weight loss in obese type 2 diabetic hemodialysis patients | ||
Medical condition: obese type 2 diabetic hemodialysis patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000541-24 | Sponsor Protocol Number: B1801381 | Start Date*: 2016-01-12 | |||||||||||
Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A Multicenter Open-Label Study of Etanercept Withdrawal and Retreatment in Subjects with Non-Radiographic Axial Spondyloarthritis who Achieved Adequate 24 Week Response | |||||||||||||
Medical condition: Spondyloarthritis (SpA) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FI (Completed) BE (Completed) PL (Completed) HU (Completed) SE (Completed) ES (Completed) NL (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001505-14 | Sponsor Protocol Number: 110808 | Start Date*: 2015-06-17 | ||||||||||||||||||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | ||||||||||||||||||||||||||||
Full Title: A phase III, randomized, controlled, single-blind study to evaluate the non-inferiority of GlaxoSmithKline Biologicals’ 10-valent pneumococcal conjugate vaccine compared to the 7-valent pneumococca... | ||||||||||||||||||||||||||||
Medical condition: Healthy volunteers (Three dose primary vaccination of healthy infants between 6 to 12 weeks of age at the time of the first vaccination against Streptococcus pneumoniae and Haemophilus influenzae t... | ||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: Outside EU/EEA | ||||||||||||||||||||||||||||
Trial results: View results |
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