- Trials with a EudraCT protocol (44,334)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,334 result(s) found.
Displaying page 1,777 of 2,217.
EudraCT Number: 2005-004153-10 | Sponsor Protocol Number: H5N1/2005/01 | Start Date*: 2005-09-22 |
Sponsor Name:OTH - Chief Medical Officer's Office | ||
Full Title: Safety and immunogenecity of NIBRG-14 H5N1 01-2005 mock-up vaccine for potencial pandemic vaccine producers in Hungary | ||
Medical condition: Immunization of healthy people against influenza H5N1 infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004744-32 | Sponsor Protocol Number: 04-SAM-01/BS554 | Start Date*: 2006-01-25 |
Sponsor Name:Merck Generics UK Ltd. | ||
Full Title: A CUMULATIVE DOSE RESPONSE STUDY TO EVALUATE THE THERAPEUTIC EQUIVALENCE OF A NEW SALMETEROL INHALATION AEROSOL CONTAINING A REPLACEMENT HFA PROPELLANT IN A PRESSURISED METERED DOSE INHALER AND EX... | ||
Medical condition: asthma bronchiale | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-000674-73 | Sponsor Protocol Number: LJP 394-90-14 | Start Date*: 2006-08-11 | |||||||||||
Sponsor Name:La Jolla Pharmaceutical Company | |||||||||||||
Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, THREE-ARM, PARALLEL-GROUP, MULTICENTER, MULTINATIONAL SAFETY AND EFFICACY TRIAL OF 300 MG AND 900 MG OF ABETIMUS SODIUM IN SYSTEMIC LUPUS ERYTHEMATOS... | |||||||||||||
Medical condition: Systemic lupus erythematosus patients with a history of renal disease | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) SK (Completed) PT (Prematurely Ended) DE (Prematurely Ended) CZ (Prematurely Ended) ES (Ongoing) IT (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002192-40 | Sponsor Protocol Number: periodld001 | Start Date*: 2006-07-13 |
Sponsor Name:Zsolt Lohinai DMD PhD | ||
Full Title: New treatment of periodontitis by inhibition of lysine decarboxilase enzyme | ||
Medical condition: healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-001694-23 | Sponsor Protocol Number: OOI/KEMB/2006-1 | Start Date*: 2006-08-21 |
Sponsor Name:National Institute of Oncology | ||
Full Title: Efficacy of cetuximab in locally advanced or metastatic adenoid cystic carcinoma. Phase II. | ||
Medical condition: Investigating the efficacy of cetuximab (Erbitux) in locally advanced or metastatic adenoid cystic carcinoma expressing EGFR. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-002645-37 | Sponsor Protocol Number: KC706-C05 | Start Date*: 2006-08-25 | |||||||||||
Sponsor Name:Kémia, Inc. | |||||||||||||
Full Title: A Phase II randomized double-blind placebo-controlled Study of KC706 in patients with rheumatoid arthritis inadequately controlled with a stable dose of methotrexate | |||||||||||||
Medical condition: Active rheumatoid arthritis (RA), patients taking stable doses of methotrexate | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001317-42 | Sponsor Protocol Number: SAG-43/SBE | Start Date*: 2008-07-09 |
Sponsor Name:Prof. Dr. Istvan Racz | ||
Full Title: Open label, uncontrolled pilot study on the effect of mucosal healing with 3 g mesalazine granules in NSAID induced small bowel enteropathy, evaluated by video capsule endoscopy after 4 weeks of tr... | ||
Medical condition: treatment of NSAID induced small bowel enteropathy | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-000811-27 | Sponsor Protocol Number: Gl-HG-szem1-07-001 | Start Date*: 2007-05-09 |
Sponsor Name:Department of Ophthalmology, SEmmelweis University | ||
Full Title: Evaluation of additional intraocular pressure reduction with once daily, evening administration of travoprost 0.004%, once daily, evening administration of travoprost 0.004%/timolol 0.5% fixed comb... | ||
Medical condition: Open-angle glaucoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-006099-39 | Sponsor Protocol Number: DE 0206 | Start Date*: 2006-12-14 |
Sponsor Name:Department of Endocrinology University of Debrecen Medical and Health Science Center | ||
Full Title: Anti-CD20 antitest alkalmazása súlyos, hagyományos kezelésekre nem reagáló endokrin orbitopátiában | ||
Medical condition: Endocrin ophthalmopathy (conventional therapy resistent). | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-006312-30 | Sponsor Protocol Number: MACPED-06-01 | Start Date*: 2007-04-05 | |||||||||||
Sponsor Name:Dept. of Ophthalmol, Semmelweis University | |||||||||||||
Full Title: A phase IV non-randomized, uncontrolled, open-label, single-center trial to evaluate the safety and efficacy of Macugen (pegaptanib sodium) given by intravitreal injections every 6 weeks in patient... | |||||||||||||
Medical condition: neovascular (wet) age-related macular degeneration (AMD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002782-12 | Sponsor Protocol Number: OOI-001 | Start Date*: 2007-08-08 | |||||||||||
Sponsor Name:National Institute of Oncology | |||||||||||||
Full Title: Open, uncontrolled, non-commercial Clinical Trial of induction chemotherapy with Cetuximab, Docetaxel, Cisplatin, 5FU followed by Cetuximab + radiotherapy in the responders in locally advance... | |||||||||||||
Medical condition: locally advanced squamous cell carcinoma of head and neck (SCCHN) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002112-26 | Sponsor Protocol Number: 139B7 | Start Date*: 2007-05-21 |
Sponsor Name:YORK Pharma GmbH | ||
Full Title: Open, single-arm phase-III study to investigate the percutaneous absorption of abafungin after topical dermal application of Abafungin cream 1.0 % (YORK Pharma GmbH) in 20 patients with tinea pedis... | ||
Medical condition: Tinea pedis interdigital | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-003977-22 | Sponsor Protocol Number: SAKK 77/06 and SASL 23 | Start Date*: 2007-10-12 | |||||||||||
Sponsor Name:Swiss Group for Clinical Cancer Research (SAKK) | |||||||||||||
Full Title: Protocol SAKK 77/06 and SASL 23 Continuous sunitinib treatment in patients with unresectable hepatocellular carcinoma A multicenter phase II trial | |||||||||||||
Medical condition: Patients with unresectable hepatocellular carcinoma, localized but surgically unresectable or metastatic | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004167-22 | Sponsor Protocol Number: PGT307 | Start Date*: 2008-01-23 | |||||||||||||||||||||
Sponsor Name:Cell Therapeutics, Inc. | |||||||||||||||||||||||
Full Title: Paclitaxel poliglumex (CT-2103)/Carboplatin vs Paclitaxel/Carboplatin for the Treatment of Chemotherapy-Naive Advanced Non-Small Cell Lung Cancer (NSCLC) in Women with Estradiol > 30 pg/ml | |||||||||||||||||||||||
Medical condition: Advanced Non-small Cell Lung Cancer (NSCLC) in women. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: HU (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006271-37 | Sponsor Protocol Number: MIRA 1/2007 | Start Date*: 2008-06-16 |
Sponsor Name:Medical and Health Science Center, University of Debrecen Dept. of Otolaryngology | ||
Full Title: Dopamin agonista pramipexol hatása tinnitusra presbyacusisban | ||
Medical condition: Tinnitus and old age presbycusis. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-006012-38 | Sponsor Protocol Number: SAKK 41/07 | Start Date*: 2009-08-04 |
Sponsor Name:SAKK (Swiss Group for Clinical Cancer Research) | ||
Full Title: Neoadjuvant radiotherapy and capecitabine with or without panitumumab in patients with advanced, K-ras unmutated rectal cancer. A randomized multicenter phase II trial. | ||
Medical condition: Advanced K-ras unmutated rectal cancer. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-002089-74 | Sponsor Protocol Number: Matyus-2008/1 | Start Date*: 2008-08-15 | |||||||||||||||||||||
Sponsor Name:Semmelweis University | |||||||||||||||||||||||
Full Title: The investigation of the effect of dihydralazine (Depressan) on macular edema of type 2 diabetes patients and of inhibition of semicarbazide-sensitive amine oxidase (SSAO). | |||||||||||||||||||||||
Medical condition: Macular edema in patients with type 2 diabetes. | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: HU (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001509-40 | Sponsor Protocol Number: BETAVASC-IV-08-1 | Start Date*: 2008-10-18 |
Sponsor Name:Hungarian Kidney Foundation | ||
Full Title: Effects of beta blockers on central arterial pressure and vascular stiffness | ||
Medical condition: Patients with hypertension and/or ischemic heart disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-006312-38 | Sponsor Protocol Number: SAKK 41/08 | Start Date*: 2009-08-05 |
Sponsor Name:SAKK (Swiss Group for Clinical Cancer Research) | ||
Full Title: Neoadjuvant radiotherapy combined with capecitabine and sorafenib in patients with advanced, K-ras mutated rectal cancer. A randomized multicenter phase I/II trial. | ||
Medical condition: Advanced K-ras mutated rectal cancer. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-007175-24 | Sponsor Protocol Number: CRFB002AHU02T | Start Date*: 2009-02-06 | |||||||||||
Sponsor Name:University of Pécs, Medical School, Department of Ophthalmology | |||||||||||||
Full Title: A randomized, controlled, two-center phase II. study assessing the efficacy and safety of intravitreal Lucentis injections in patients with clinically significant macular edema secondary to central... | |||||||||||||
Medical condition: Macular edema secondary to central retinal vein occlusion | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: (No results available) |
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