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Laatste proeven
EudraCT Number: 2006-000606-23 | Sponsor Protocol Number: 26756 | Start Date: 2006-11-23 | |||||||||||
Sponsor Name: Merck, S.L. | |||||||||||||
Full Title: Post-authorization safety study to check the potential association between the safety profile of beta interferon 1a and the body mass index or pharmacodynamics during the titration phase | |||||||||||||
Medical condition: Not applicalbe | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003512-22 | Sponsor Protocol Number: 0869-130 | Start Date: 2006-11-23 | ||||||
Sponsor Name: Laboratoires Merck Sharp & Dohme-Chibret | ||||||||
Full Title: A Randomized, Double-Blind, Parallel-Group Study Conducted Under In-House Blinding Conditions to Determine the Efficacy and Tolerability of Aprepitant for the Prevention of Chemotherapy-Induced Nau... | ||||||||
Medical condition: Chemotherapy-induced Nausea and Vomitting | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: FR (Completed) DE (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2005-003819-71 | Sponsor Protocol Number: DX-88/14 | Start Date: 2006-11-23 | ||||||
Sponsor Name: Dyax Corp | ||||||||
Full Title: EDEMA3: Evaluation of DX-88’s Effects in Mitigating Angioedema A double-blind, placebo-controlled study followed by a repeat dosing phase to assess the efficacy and safety of DX-88 (recombinant pl... | ||||||||
Medical condition: Hereditary Angioedema | ||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: BE (Completed) GB (Completed) IT (Completed) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001595-20 | Sponsor Protocol Number: CRAD001J2102 | Start Date: 2006-11-23 | |||||||||||
Sponsor Name: NOVARTIS FARMA | |||||||||||||
Full Title: A phase Ib study investigating the combination of RAD001 with trastuzumab and vinorelbine in patients with HER2- overexpressing metastatic breast cancer | |||||||||||||
Medical condition: HER2 overexpressing metastatic breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002335-24 | Sponsor Protocol Number: 13362B | Start Date: 2006-11-23 | ||||||
Sponsor Name: University of Chicago | ||||||||
Full Title: A Phase III Randomized Trial of Docetaxel Based Induction Chemotherapy in Patients with N2/N3 Locally Advanced Head and Neck Cancer Estudio de fase III randomizado de una quimioterapia de inducción... | ||||||||
Medical condition: Phase III trial of induction therapy with docetaxel followed by chemoradiotherapy versus chemoradiotherapy alone in patients with nodal stage N2 or N3 head and neck cancer | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: ES (Ongoing) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005494-21 | Sponsor Protocol Number: MARIA | Start Date: 2006-11-23 | |||||||||||
Sponsor Name: HYKS Marian sairaala | |||||||||||||
Full Title: Hyperbaarisen artikaiini-glukoosiliuoksen ja pelkän artikaiinin vertailu spinaalipuudutuksessa nivustyräpotilailla | |||||||||||||
Medical condition: nivustyrä | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005127-42 | Sponsor Protocol Number: APIDR_L_01896 | Start Date: 2006-11-22 | |||||||||||
Sponsor Name: Institut für Klinische Forschung und Entwicklung (ikfe) GmbH | |||||||||||||
Full Title: Effect of Prandial Treatment with Insulin Glulisine compared to Regular Human Insulin on Postprandial Endothelial Function and Microvascular Stress in Type 2 Diabetic Patients | |||||||||||||
Medical condition: Diabetes mellitus Type 2 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003632-22 | Sponsor Protocol Number: WA19078 | Start Date: 2006-11-22 | ||||||
Sponsor Name: F. Hoffmann-La Roche Ltd. | ||||||||
Full Title: An open-label, exploratory study of the pharmacokinetic and pharmacodynamic activity of rituximab in combination with methotrexate (MTX) in synovial tissue and in peripheral blood of patients with ... | ||||||||
Medical condition: Rheumatoid arthritis | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: ES (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2006-002679-42 | Sponsor Protocol Number: SNT-II-003 | Start Date: 2006-11-22 | ||||||
Sponsor Name: Santhera Pharmaceuticals (Switzerland) Limited | ||||||||
Full Title: A double blind, randomised, placebo-controlled study of the efficacy, safety and tolerability of idebenone in the treatment of patients with Leber's Hereditary Optic Neuropathy | ||||||||
Medical condition: Leber's Hereditary Optic Neuropathy | ||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||
Trial protocol: GB (Completed) DE (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2006-000679-14 | Sponsor Protocol Number: Mio/Reg/percutáneo/Aleatorizado | Start Date: 2006-11-22 | |||||||||||
Sponsor Name: INSTITUTO CIENTÍFICO Y TECNOLÓGICO (ICT )DE NAVARRA, S.A. | |||||||||||||
Full Title: ESTUDIO DE FASE II CIEGO, CONTROLADO Y ALEATORIZADO DE EFICACIA DEL IMPLANTE PERCUTÁNEO DE MIOBLASTOS AUTÓLOGOS EN PACIENTES CON INFARTO ANTIGUO. (STUDY PHASE II BLINDED, CONTROLATED AND RANDOMIZED... | |||||||||||||
Medical condition: PACIENTES CON INFARTO ANTIGUO DE MIOCARDIO (PATIENTS WITH OLD MYOCARDIAL INFARCT) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |