- Trials with a EudraCT protocol (10,987)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
10,987 result(s) found.
Displaying page 269 of 550.
| EudraCT Number: 2007-004875-21 | Sponsor Protocol Number: BAY 43-9006 / 12913 | Start Date*: 2008-01-21 | |||||||||||
| Sponsor Name:Bayer Healthcare AG, D-51368 Leverkusen, Germany | |||||||||||||
| Full Title: A Phase II, Multi-centre, Open-label Study to Assess the Efficacy, Safety, Tolerability and Pharmacokinetics of Intrapatient Dose Escalation of Sorafenib as First Line Treatment for Metastatic Rena... | |||||||||||||
| Medical condition: renal cell carcinoma | |||||||||||||
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| Population Age: | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) IT (Completed) GB (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-005234-36 | Sponsor Protocol Number: NR001-03 | Start Date*: 2008-11-20 | |||||||||||
| Sponsor Name:NovaRx Corporation | |||||||||||||
| Full Title: Registration Phase III Study of Lucanix™ (Belagenpumatucel-L) in Advanced Non-small Cell Lung Cancer: An International Multicenter, Randomized, Double-blinded, Placebo-controlled Study of Lucanix™... | |||||||||||||
| Medical condition: Non Small Cell Lung Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) DE (Prematurely Ended) HU (Prematurely Ended) NL (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-000876-26 | Sponsor Protocol Number: CLIN801 PCM201 | Start Date*: 2008-05-02 | |||||||||||
| Sponsor Name:STEBA BIOTECH NV | |||||||||||||
| Full Title: "VASCULAR-TARGETED PHOTODYNAMIC THERAPY USING WST11 IN PATIENTS WITH LOCALISED PROSTATE CANCE" | |||||||||||||
| Medical condition: The Treatment of prostate cancer. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: FR (Ongoing) GB (Completed) NL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-005933-12 | Sponsor Protocol Number: E7080-G000-201 | Start Date*: 2009-10-29 | |||||||||||
| Sponsor Name:Eisai Limited | |||||||||||||
| Full Title: Phase II, Multicenter, Open-label, Single Arm Trial to Evaluate the Safety and Efficacy of Oral E7080 in Medullary and Iodine-131 Refractory, Unresectable Differentiated Thyroid Cancers, Stratified... | |||||||||||||
| Medical condition: Medullary thyroid cancer [MTC] or radioiodine (131*I) refractory/resistant differentiated thyroid cancer[DTC]: Determine the pharmacokinetic (PK) profile and the pharmacokinetic/pharmacodynamic (PK... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) PL (Completed) GB (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-013097-40 | Sponsor Protocol Number: NP031112-08B02 | Start Date*: 2009-10-30 | ||||||||||||||||
| Sponsor Name:Noscira S.A. | ||||||||||||||||||
| Full Title: A double-blind, placebo-controlled, randomized, parallel-group study evaluating the safety, tolerability and efficacy of two different oral doses of NP031112, a GSK-3 inhibitor, versus placebo in t... | ||||||||||||||||||
| Medical condition: Mild to Moderate Progressive Supranuclear Palsy | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) ES (Completed) DE (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2009-010198-19 | Sponsor Protocol Number: CLCQ908A2204 | Start Date*: 2009-05-27 | ||||||||||||||||
| Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
| Full Title: A Phase 2 12-week multi-center, randomized, double-blind, placebo-controlled, parallel-group adaptive design study to evaluate the safety and efficacy of LCQ for weight reduction and reduced LDL ch... | ||||||||||||||||||
| Medical condition: Obesity and mixed dyslipidemia | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: SE (Prematurely Ended) GB (Completed) ES (Completed) DK (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2009-015773-12 | Sponsor Protocol Number: 6096-011 | Start Date*: 2010-01-08 | |||||||||||
| Sponsor Name:Merck & Co. Inc. | |||||||||||||
| Full Title: A Phase IIb, Multicenter, Randomized, Double-Blind, Placebo-Controlled, 2-Period Adaptive Crossover Polysomnography Study to Evaluate the Safety and Efficacy of MK 6096 in Patients with Primary Ins... | |||||||||||||
| Medical condition: Primary insomnia | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) DE (Completed) FI (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-001361-29 | Sponsor Protocol Number: CLWP 001 2008 | Start Date*: 2009-10-08 | |||||||||||
| Sponsor Name:EBMT (European group for Blood and Marrow Transplantation) | |||||||||||||
| Full Title: Phase II efficacy and safety study of Dasatinib in Patients with Chronic and Accelerated Phase Chronic Myeloid Leukaemia Relapsing after Allogeneic Blood or Bone Marrow Transplantation | |||||||||||||
| Medical condition: chronic myeloid leukaemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) GB (Prematurely Ended) DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-014415-12 | Sponsor Protocol Number: MEA112997 | Start Date*: 2010-01-04 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
| Full Title: A multicentre, randomised, double-blind, placebo-controlled, parallel group, dose ranging study to determine the effect of mepolizumab on exacerbation rates in subjects with severe uncontrolled ref... | |||||||||||||
| Medical condition: severe uncontrolled refractory asthma. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) GB (Completed) FR (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-003772-21 | Sponsor Protocol Number: MPP111782 | Start Date*: 2009-05-06 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
| Full Title: A TWO-PART, RANDOMISED, DOUBLE-BLIND, PLACEBO CONTROLLED, MULTI-CENTER STUDY TO INVESTIGATE THE USE OF MEPOLIZUMAB (SB-240563) IN REDUCING THE NEED FOR SURGERY IN SUBJECTS WITH SEVERE BILATERAL NAS... | |||||||||||||
| Medical condition: Nasal polyposis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) GB (Completed) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-014660-19 | Sponsor Protocol Number: RDEA594-203 | Start Date*: 2009-12-09 | |||||||||||
| Sponsor Name:Ardea Biosciences, Inc. | |||||||||||||
| Full Title: Randomized, Double-Blind, Multicenter, Placebo-Controlled, Combination Study to Evaluate the Safety, Efficacy and Potential Pharmacokinetic Interaction of RDEA594 and Allopurinol in Gout Patients w... | |||||||||||||
| Medical condition: Gout | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) ES (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-006494-90 | Sponsor Protocol Number: M06-807 | Start Date*: 2008-11-24 | |||||||||||
| Sponsor Name:Abbvie Deutschland GmbH & Co. K.G. | |||||||||||||
| Full Title: A Multi-center, Open-label Study of the Human Anti−TNF Monoclonal Antibody Adalimumab to Evaluate the Efficacy and the Long-term Safety and Tolerability of Repeated Administration of Adalimumab in ... | |||||||||||||
| Medical condition: Crohn's disease | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) CZ (Completed) GB (Completed) Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-011398-33 | Sponsor Protocol Number: NN1250-3724 | Start Date*: 2010-01-27 | |||||||||||
| Sponsor Name:Novo Nordisk A/S | |||||||||||||
| Full Title: BEGIN™: EASY AM A trial comparing efficacy and safety of NN1250 and insulin glargine in subjects with type 2 diabetes | |||||||||||||
| Medical condition: Type 2 Diabetes | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) SK (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-013030-25 | Sponsor Protocol Number: GE-067-007 | Start Date*: 2010-05-12 | |||||||||||
| Sponsor Name:GE Healthcare Ltd. and its Affiliates | |||||||||||||
| Full Title: A Principal Open-Label Study to Compare the Brain Uptake of [18F]flutemetamol with Brain Amyloid Levels Determined Post-Mortem | |||||||||||||
| Medical condition: The subjects have a short life expectancy. GE-067-007 will determine the level of association between brain uptake of (18F)flutemetamol and brain amyloid levels. Assessments will be based on analy... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) GB (Completed) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-016713-20 | Sponsor Protocol Number: CL2-20098-072 | Start Date*: 2010-04-13 | |||||||||||
| Sponsor Name:Laboratorios Servier S.L. | |||||||||||||
| Full Title: Eficacia de agomelatina 25mg/día (con posibilidad de incremento a 50mg/día tras 8 semanas de tratamiento) por vía oral durante 16 semanas en pacientes con Trastorno Obsesivo Compulsivo // Efficacy... | |||||||||||||
| Medical condition: Trastorno Obsesivo Compulsivo // Obsessive-compulsive disorder | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) SE (Completed) GB (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-019634-26 | Sponsor Protocol Number: MPEX-209 | Start Date*: 2011-05-24 | ||||||||||||||||
| Sponsor Name:Mpex Pharmaceuticals, Inc. | ||||||||||||||||||
| Full Title: A Phase 3, Open-Label, Randomized Trial to Evaluate the Safety and Efficacy of MP-376 Inhalation Solution (Aeroquin™) versus Tobramycin Inhalation Solution (TIS) in Stable Cystic Fibrosis Patients | ||||||||||||||||||
| Medical condition: Pseudomonas aeruginosa infection in patients suffering from stable Cystic Fibrosis | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) GB (Completed) FR (Ongoing) IE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2010-023442-75 | Sponsor Protocol Number: DB2114417 | Start Date*: 2011-04-28 | |||||||||||
| Sponsor Name:GlaxoSmithKline | |||||||||||||
| Full Title: An exercise endurance study to evaluate the effects of treatment of COPD patients with a dual bronchodilator: GSK573719/GW642444 | |||||||||||||
| Medical condition: Moderate/severe chronic obstructive pulmonary disease (COPD). | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) GB (Completed) EE (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-024244-15 | Sponsor Protocol Number: RDG-10-251 | Start Date*: 2011-07-01 | |||||||||||
| Sponsor Name:ALCON Research Ltd | |||||||||||||
| Full Title: "Patient Preference Comparison of Azarga versus Cosopt, in Patients with Open-Angle Glaucoma or Ocular Hypertension." | |||||||||||||
| Medical condition: Open-Angle Glaucoma and Ocular Hypertension | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) GB (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-021057-39 | Sponsor Protocol Number: NN2211-1800 | Start Date*: 2010-11-11 | |||||||||||
| Sponsor Name:Novo Nordisk A/S | |||||||||||||
| Full Title: A Randomized, Double-blind, Placebo Controlled Trial to Assess Safety/Tolerability, Pharmacokinetics & Pharmacodynamics of Liraglutide in Paediatric (10 – 17 years old) Subjects with Type 2 Diabetes | |||||||||||||
| Medical condition: Type 2 Diabetes | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) SI (Completed) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-018118-21 | Sponsor Protocol Number: OXN2503 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Mundipharma Research GmbH & Co. KG | |||||||||||||
| Full Title: An exploratory, randomised, double-blind, placebo-controlled, parallel group, pilot study to assess the analgesic efficacy of oxycodone/naloxone prolonged release tablets (OXN PR) compared to place... | |||||||||||||
| Medical condition: Bladder Pain Syndrome (BPS), formerly addressed as IC/PBS (interstitial cystitis /Painful Bladder Syndrome) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: DE (Completed) HU (Completed) CZ (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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