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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...
Disease: Version SOC Term Classification Code Term Level
6.0 10055221 LLT
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)
Disease: Version SOC Term Classification Code Term Level
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
Disease: Version SOC Term Classification Code Term Level
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
Disease: Version SOC Term Classification Code Term Level
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
Disease: Version SOC Term Classification Code Term Level
9.1 10028228 Multiple myeloma LLT
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
Disease: Version SOC Term Classification Code Term Level
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
Disease: Version SOC Term Classification Code Term Level
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)
Disease: Version SOC Term Classification Code Term Level
7.0 10048780 PT
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).
Disease: Version SOC Term Classification Code Term Level
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 ...
Disease: Version SOC Term Classification Code Term Level
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: IE (Completed)
Trial results: View results
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