- Trials with a EudraCT protocol (44,347)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,347 result(s) found.
Displaying page 798 of 2,218.
EudraCT Number: 2012-005183-94 | Sponsor Protocol Number: CLAF237AFR07 | Start Date*: 2013-03-25 | |||||||||||
Sponsor Name:Novartis Pharma S.A.S. | |||||||||||||
Full Title: Etude multicentrique, randomisée, contrôlée, en ouvert d'une durée de 24 semaines, comparant la stratégie metformine/vildagliptine + insuline basale versus metformine/sulfamide + insuline basale ch... | |||||||||||||
Medical condition: Diabète de type II | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003041-10 | Sponsor Protocol Number: CRFB002H2301 | Start Date*: 2015-04-14 | |||||||||||
Sponsor Name:NOVARTIS FARMA S.p.A. | |||||||||||||
Full Title: RAINBOW study: a randomized, controlled study evaluating the efficacy and safety of RAnibizumab compared with laser therapy for the treatment of INfants BOrn prematurely With retinopathy of prematu... | |||||||||||||
Medical condition: Retinopathy of prematurity (ROP) | |||||||||||||
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Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) EE (Completed) LT (Completed) HU (Completed) BE (Completed) AT (Completed) DE (Completed) GB (Completed) HR (Completed) FR (Completed) SK (Completed) CZ (Completed) GR (Completed) DK (Completed) FI (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-006066-34 | Sponsor Protocol Number: 105987,105988 | Start Date*: 2015-06-01 | |||||||||||||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||||||||||||
Full Title: A phase III, single-blind, randomized, controlled, multinational study for the evaluation of safety of GSK Biologicals' Haemophilus influenzae type b and Neisseria meningitidis serogroups C and Y-t... | |||||||||||||||||||||||
Medical condition: Haemophilus influenzae type b and Neisseria meningitidis serogroups C and Y | |||||||||||||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-000276-10 | Sponsor Protocol Number: FAST2015 | Start Date*: 2015-07-02 |
Sponsor Name:FAST Consortium under EU 7. FWP | ||
Full Title: FAST – Food Allergy Specific ImmunoTherapy A multinational phase IIb study to investigate the efficacy and safety of subcutaneous immunotherapy with a modified fish- parvalbumin given in single ri... | ||
Medical condition: Food allergy to fish | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: IS (Completed) DK (Completed) GR (Ongoing) NL (Completed) PL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002758-11 | Sponsor Protocol Number: D4420C00005 | Start Date*: 2015-10-21 | |||||||||||
Sponsor Name:MedImmune, LLC | |||||||||||||
Full Title: A Phase 2b Randomized, Double-blind Study to Evaluate the Efficacy of MEDI7510 for the Prevention of Acute Respiratory Syncytial Virus-associated Respiratory Illness in Older Adults | |||||||||||||
Medical condition: Prevention of Acute Respiratory Syncytial Virus-associated Respiratory Illness | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Prematurely Ended) LV (Prematurely Ended) EE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001356-31 | Sponsor Protocol Number: PEN-PV | Start Date*: 2015-05-20 | |||||||||||
Sponsor Name:AOP Orphan Pharmaceuticals AG | |||||||||||||
Full Title: An open-label, single arm, Phase III study to assess the self-administration of AOP2014 using a pre-filled pen, developed for the treatment of Polycythemia Vera patients | |||||||||||||
Medical condition: Polycythemia Vera | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) SK (Completed) AT (Completed) CZ (Completed) BG (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005545-12 | Sponsor Protocol Number: | Start Date*: 2012-03-02 | |||||||||||
Sponsor Name:University of Leicester | |||||||||||||
Full Title: Enhanced Control of Hypertension and Thrombolysis Stroke Trial | |||||||||||||
Medical condition: Acute Ischaemic Stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002718-38 | Sponsor Protocol Number: 111670 | Start Date*: 2015-06-10 | ||||||||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | ||||||||||||||||||
Full Title: A phase II, open, controlled, multi-center study to evaluate the long-term antibody persistence at 1 year, 3 years and 5 years after the administration of one dose of GlaxoSmithKline (GSK) Biologic... | ||||||||||||||||||
Medical condition: Invasive disease caused by Neisseria meningitidis serogroups A, C W-135 and Y | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: Outside EU/EEA | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-001554-15 | Sponsor Protocol Number: 2014_01 | Start Date*: 2015-08-13 |
Sponsor Name:CHRU de Lille | ||
Full Title: Study controls feasibility of an intrapleural photodynamic therapy integrated into a multimode treatment associating a pleurectomy/extended hulling, a radiotherapy and an auxiliary chemotherapy amo... | ||
Medical condition: Malignant pleural mesothelioma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003048-37 | Sponsor Protocol Number: HSJC-CAR-01-2015 | Start Date*: 2015-11-13 |
Sponsor Name:Juan Luis Bonilla Palomas | ||
Full Title: Effect of ?-3 polyunsaturated fatty acids on serum albumin concentration in patients with acute heart failure, hypoalbuminemia, and high inflammatory activity | ||
Medical condition: Heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003492-36 | Sponsor Protocol Number: PS0003 | Start Date*: 2015-03-12 | |||||||||||
Sponsor Name:UCB Biopharma, SPRL | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo- And Active-Controlled Study Followed By A Placebo-Controlled Maintenance Period And Open-Label Follow-Up To Evaluate The E... | |||||||||||||
Medical condition: Plaque Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) HU (Completed) CZ (Completed) NL (Completed) PL (Completed) BG (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005718-20 | Sponsor Protocol Number: 111315 | Start Date*: 2015-04-01 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A phase 2, open, randomized, controlled, multi-center study to evaluate the safety and immunogenicity of 7 infant immunization schedules of the RTS,S/AS01E candidate vaccine against P. falciparum. | ||
Medical condition: Healthy volunteers (Primary immunization against Plasmodium falciparum malaria) | ||
Disease: | ||
Population Age: Newborns, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2014-000933-21 | Sponsor Protocol Number: B1971017 | Start Date*: 2015-07-06 | |||||||||||
Sponsor Name:Pfizer Inc, 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A PHASE 2, RANDOMIZED, CONTROLLED, OBSERVER-BLINDED STUDY TO DESCRIBE THE IMMUNOGENICITY, SAFETY, AND TOLERABILITY OF NEISSERIA MENINGITIDIS SEROGROUP B BIVALENT RECOMBINANT LIPOPROTEIN 2086 VACCIN... | |||||||||||||
Medical condition: Invasive meningococcal disease (IMD) caused by Neisseria meningitidis serogroup B | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002523-42 | Sponsor Protocol Number: D3250C00020 | Start Date*: 2014-06-24 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A multicenter, randomized, double-blind, parallel group, placebo-controlled, Phase 3 efficacy and safety study of benralizumab (MEDI-563) to reduce oral corticosteroid use in patients with uncontro... | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) PL (Completed) ES (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004281-25 | Sponsor Protocol Number: MLN1117-1501 | Start Date*: 2015-08-25 | |||||||||||
Sponsor Name:Millennium Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 1b/Adaptive Phase 2 Study of Docetaxel With or Without MLN1117 in Patients With Locally Advanced or Metastatic Non-small Cell Lung Cancer | |||||||||||||
Medical condition: non-small cell lung cancer (NSCLC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) NL (Ongoing) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000582-31 | Sponsor Protocol Number: AGLU3306 | Start Date*: 2015-04-15 | |||||||||||
Sponsor Name:Genzyme Corporation Inc | |||||||||||||
Full Title: An Exploratory, Open-Label Study of the Safety and Efficacy of High Dose or High Dosing Frequency Myozyme® (alglucosidase alfa) Treatment in Patients with Pompe Disease Who Do Not Have an Optimal R... | |||||||||||||
Medical condition: Pompe disease (acid alpha-glucosidase deficiency) | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002780-42 | Sponsor Protocol Number: TR701-111 | Start Date*: 2015-06-29 | |||||||||||
Sponsor Name:Trius Therapeutics [...] | |||||||||||||
Full Title: A Phase 1, Open-Label, Multi-Center, Two-Part, Single-Dose, Parallel Design, Safety, Tolerance, and Pharmacokinetic Study of Orally and Intravenously Administered TR-701 FA in 12 to 17 Year Old Ad... | |||||||||||||
Medical condition: Acute bacterial skin and skin structure infections | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005272-34 | Sponsor Protocol Number: 42703 | Start Date*: 2013-01-28 |
Sponsor Name:Nederlandse Vereniging van Artsen voor Longziekten en Tuberculose NVALT | ||
Full Title: Iressa RE-challenge in advanced NSCLC EGFR mutated patients who responded to an EGFR-TKI used as first-line or previous treatment. | ||
Medical condition: Non small cell lung cancer | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-012897-12 | Sponsor Protocol Number: BIA-91067-202 | Start Date*: 2009-12-08 | |||||||||||
Sponsor Name:BIAL-Portela & Ca, SA | |||||||||||||
Full Title: A double-blind, randomised, placebo-controlled study to investigate the tolerability and the effect of three multiple-dose regimens of BIA 9-1067 on the levodopa pharmacokinetics, catechol-0-methyl... | |||||||||||||
Medical condition: Parkinson’s Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000370-19 | Sponsor Protocol Number: CO-1686-022 | Start Date*: 2015-01-14 | |||||||||||
Sponsor Name:Clovis Oncology, Inc. | |||||||||||||
Full Title: TIGER-1: A Randomized, Open-Label, Phase 2/3 Study of CO-1686 or Erlotinib as First-Line Treatment of Patients with EGFR-Mutant Advanced/Metastatic Non-Small Cell Lung Cancer (NSCLC) | |||||||||||||
Medical condition: First-Line Treatment of Patients with EGFR-Mutant Advanced Non-Small Cell Lung Cancer (NSCLC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) FR (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
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