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Najnowsze wersje próbne
EudraCT Number: 2004-000452-16 | Sponsor Protocol Number: 156-03-244 | Start Date: 2004-08-02 | |||||||||||
Sponsor Name: Otsuka Maryland Research Institute | |||||||||||||
Full Title: International, Multi-Centre, Study of One year, Open Label, Titrated Oral Tolvaptan Tablet Administration in Patients with Chronic Hyponatraemia: Extension to Studies 156-02-235 and 156-03-238 to a... | |||||||||||||
Medical condition: Ongoing hyponatraemia in euvolemic and hypervolemic states | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) CZ (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000312-93 | Sponsor Protocol Number: 0431-020 | Start Date: 2004-08-02 | |||||||||||
Sponsor Name: Merck Sharp & Dohme (Sweden) AB | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind Study to Evaluate the Safety and Efficacy of the Addition of MK-0431 to Patients with Type 2 Diabetes Mellitus Who Have Inadequate Glycemic Control on Metfor... | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) AT (Completed) DK (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001273-26 | Sponsor Protocol Number: CASM981CES02 | Start Date: 2004-08-02 | |||||||||||
Sponsor Name: NOVARTIS FARMACEUTICA, S.A | |||||||||||||
Full Title: A 3 weeks study randomized, multicenter, double blind, vehicle controlled , parallel-group to evaluate the efficacy and safety of Pimecrolimus cream 1% in children between 2 – 11 years with mild to... | |||||||||||||
Medical condition: Mild to moderate Atopic Dermatitis | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002033-39 | Sponsor Protocol Number: PAN 2004-01 | Start Date: 2004-08-02 | |||||||||||
Sponsor Name: AZIENDA OSPEDALIERA SAN GERARDO DI MONZA | |||||||||||||
Full Title: STUDY OF PREOPERATIVE AND POSTOPERATIVE IL-2 IMMUNOTHERAPY IN PANCREATIC CANCER SURGERY - RANDOMIZED PHASE 2 STUDY | |||||||||||||
Medical condition: PREVENTION OF IMMUNODEFICENCY IN PANCREATIC CANCER UNDERGOING SURGERY | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001548-60 | Sponsor Protocol Number: MA17903 | Start Date: 2004-08-02 | ||||||
Sponsor Name: F. Hoffmann-La Roche Ltd | ||||||||
Full Title: Double-blind, partially randomized, parallel group, multicenter study to assess the efficacy and safety of 100 mg and 150 mg monthly oral ibandronate in women with postmenopausal osteoporosis havin... | ||||||||
Medical condition: Long term study in women with postmenopausal osteoporosis. | ||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||
Trial protocol: HU (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-000718-37 | Sponsor Protocol Number: RA/PR/033001/005/04 | Start Date: 2004-07-30 | |||||||||||
Sponsor Name: Chiesi Farmaceutici S.p.A. | |||||||||||||
Full Title: Double blind, double dummy, multinational, multicenter, parallel-group design clinical trial of superiority of CHF 1535 1 puff in a b.i.d regimen administered via an HFA-propellant-pMDI versus a do... | |||||||||||||
Medical condition: Mild to moderate adult asthmatic patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000148-26 | Sponsor Protocol Number: SP516 | Start Date: 2004-07-30 | ||||||
Sponsor Name: Schwarz BioSciences Inc. | ||||||||
Full Title: A multi-centre, multinational, phase 3, open-label extension trial to assess the safety of long-term treatment of rotigotine patch in subjects with advanced stage, idiopathic Parkinson's disease wh... | ||||||||
Medical condition: Parkinson's Disease | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: FI (Completed) SE (Completed) HU (Completed) ES (Completed) CZ (Completed) IT (Completed) AT (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-001673-25 | Sponsor Protocol Number: VALSARTAN-TRAPIANTO/04 | Start Date: 2004-07-30 | |||||||||||
Sponsor Name: OSPEDALE S. RAFFAELE | |||||||||||||
Full Title: EFFECTS OF ANGIOTENSIN RECEPTOR ANTAGONIST ON CHRONIC NEPHROPATY IN KIDNEY TRANSPLANTED PATIENTS. A PILOT STUDY. | |||||||||||||
Medical condition: CHRONIC NEPHROPATY REDUCTION | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001347-37 | Sponsor Protocol Number: GIMEMAAML17(EORTC06012) | Start Date: 2004-07-30 | |||||||||||
Sponsor Name: G.I.M.E.M.A. GRUPPO ITALIANO MALATTIE EMATOLOGICHE DELL'ADULTO | |||||||||||||
Full Title: Gemtuzumab ozogamicin (GO) combined with standard intensive chemotherapy versus standard intensive chemotherapy alone for induction/consolidation in patients 61-75 years old with previously untre... | |||||||||||||
Medical condition: Previously untreated primary or secondary AML (including AML after MDS).All FAB subtypes except M3.No AML supervening after other myeloproliferative diseases.Age 61-75 years. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000383-27 | Sponsor Protocol Number: D1803C00002 | Start Date: 2004-07-28 | ||||||
Sponsor Name: AstraZeneca AB | ||||||||
Full Title: A double-blind randomized placebo controlled crossover study of AZD7371 ER 5 mg bid, 20 mg bid and placebo treatment for one week on visceral perception and symptoms in patients with Irritable Bowe... | ||||||||
Medical condition: Irritable Bowel Syndrome (IBS) | ||||||||
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Population Age: Adults | Gender: Male, Female | |||||||
Trial protocol: SE (Completed) | ||||||||
Trial results: View results |