- ICH GCP
- EUs kliniske prøveregister
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EudraCT Number: 2004-001729-11 | Sponsor Protocol Number: CR040301 | Start Date: 2005-02-18 | |||||||||||
Sponsor Name: EBEWE Pharma Ges.m.b.H Nfg.KG | |||||||||||||
Full Title: A prospective, randomised, placebo controlled, double blind trial about safety and efficacy of combined treatment with Alteplase (rt-PA) and Cerebrolysin in acute ischemic hemispheric stroke | |||||||||||||
Medical condition: Clinical diagnosis of ischemic stroke causing a measurable neurological deficit defined as impairment of language, motor function, cognition and/or gaze, vision or neglect. Ischemic stroke is defin... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) SK (Completed) CZ (Completed) SI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002165-20 | Sponsor Protocol Number: 20040110 | Start Date: 2005-02-18 | ||||||
Sponsor Name: Amgen Inc | ||||||||
Full Title: An open label study of AMG 706 in subjects with advanced gastrointestinal stromal tumors (GISTs) who developed progressive disease or relapsed while on Imatinib Mesylate. | ||||||||
Medical condition: Gastrointestinal stromal tumour (GIST) | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: GB (Completed) DE (Completed) IT (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-002798-21 | Sponsor Protocol Number: WI18273 | Start Date: 2005-02-18 | ||||||
Sponsor Name: F.Hoffmann-La Roche Ltd | ||||||||
Full Title: A Phase II, prospective, randomized, double-blind, active-controlled, parallel group, multi-center 'proof of concept' trial in adult patients with community-acquired pneumonia requiring hospitaliza... | ||||||||
Medical condition: Community-acquired pneumonia | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: LV (Completed) HU (Completed) SK (Completed) LT (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-005045-35 | Sponsor Protocol Number: CLAF237A2327 | Start Date: 2005-02-17 | ||||||
Sponsor Name: Novartis Sverige AB | ||||||||
Full Title: A multicenter, randomized, double-blind, active controlled study to compare the effect of 24 weeks treatment with LAF237 50 mg bid to rosiglitazone 8 mg qd in drug naïve patients with type 2 diabetes | ||||||||
Medical condition: Type II Diabetes | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: SE (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-002102-30 | Sponsor Protocol Number: CC-5013-MM-012 | Start Date: 2005-02-17 | |||||||||||
Sponsor Name: CELGENE EUROPE LIMITED | |||||||||||||
Full Title: OPEN-LABEL, SINGLE-ARM STUDY OF THE SAFETY AND EFFICACY OF CC-5013 MONOTHERAPY FOR SUBJECTS WITH MULTIPLE MYELOMA A COMPANION STUDY FOR STUDIES THAL-MM-003, CC-5013-MM-009, AND CC-5013-MM-010 | |||||||||||||
Medical condition: Multiple Myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-003761-33 | Sponsor Protocol Number: IDT.ES.LEV.12004-EMDE | Start Date: 2005-02-17 | ||||||
Sponsor Name: Unidad de Neuroinmunología | ||||||||
Full Title: Unicenter double-blind, cross-over, randomised, placebo controlled clinical trial to evaluate efficacy of vardenafil in subjects with E.D. and multiple sclerosis (M.S.) | ||||||||
Medical condition: Erectile Dysfunction | ||||||||
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Population Age: Adults | Gender: Male | |||||||
Trial protocol: ES (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-002633-39 | Sponsor Protocol Number: SHCS-Projekt Nr. 408 | Start Date: 2005-02-17 | ||||||
Sponsor Name: Prof. Dr. med. Milos Opravil, Universitätsspital Zürich | ||||||||
Full Title: Prospective study of switch to 3TC monotherapy with evaluation of replication capacity in patients with virologic failure and 3TC resistance (a multicenter prospective clinical study within the SH... | ||||||||
Medical condition: HIV patients with virological treatment failure due to multi-drug-resistant virus including 3TC resistance | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: DE (Ongoing) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001845-13 | Sponsor Protocol Number: Y-47-52120-722 | Start Date: 2005-02-17 | |||||||||||
Sponsor Name: Beaufour Ipsen Pharma S.A.S. | |||||||||||||
Full Title: A phase II, multicentre, multinational, prospective, randomised, double-blind, placebo controlled study assessing the efficacy and safety of a single application of three doses of Dysport in patien... | |||||||||||||
Medical condition: Upper back myofascial pain syndrome (MPS) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) CZ (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004130-14 | Sponsor Protocol Number: IMA 04001 | Start Date: 2005-02-17 | ||||||
Sponsor Name: Biogen Idec GmbH | ||||||||
Full Title: A multicenter, randomized, rater-blind study to compare the efficacy and safety of natalizumab (300 mg IV every four weeks) with Interferon beta-1a (44 mcg SC three times a week) in subjects with r... | ||||||||
Medical condition: Male and female subjects with relapsing multiple sclerosis previously treated with interferon beta-1a (22 mcg or 44 mcg, SC three times a week). | ||||||||
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Population Age: Adults | Gender: Male, Female | |||||||
Trial protocol: AT (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-001862-42 | Sponsor Protocol Number: MeBN/02/Zof-AMI/001 | Start Date: 2005-02-17 | ||||||
Sponsor Name: Clinical Research Facilities | ||||||||
Full Title: A multicenter, double-blind, randomized 2x2 factorial design study to compare the efficacy of early ( | ||||||||
Medical condition: Study population: Subjects undergoing a primary percutaneous coronary intervention (PCI) to be performed within 6 hours after the onset of symptoms of a first acute anterior myocardial infarction ... | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: IE (Completed) | ||||||||
Trial results: View results |