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Latest Trials
EudraCT Number: 2004-004722-27 | Sponsor Protocol Number: ICT-BEM-2004-01 | Start Date: 2005-05-12 | |||||||||||
Sponsor Name: Instituto Científico y Tecnológico de Navarra, S.A. | |||||||||||||
Full Title: Randomised, open, multicenter, sequential trial assessing the safety and efficacy of bemiparin on the response to the treatment in patients diagnosed with localized small cell carcinoma of the lung. | |||||||||||||
Medical condition: Small cell carcionoma of the lung medDRA CLASSIFICATION CODE: PT 10041071 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000980-93 | Sponsor Protocol Number: I-ICRNS-003-VLPNX-01 | Start Date: 2005-05-12 | |||||||||||
Sponsor Name: CRINOS S.P.A. | |||||||||||||
Full Title: A randomised, double blind, multicentre Italian study, to assess the efficacy and tolerability of octatropine methilbromide in combination with diazepam(Valpinax) compared versus placebo in the tre... | |||||||||||||
Medical condition: vascular disease at thrombotic risk | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001459-39 | Sponsor Protocol Number: DIV-01/04 | Start Date: 2005-05-12 | |||||||||||
Sponsor Name: SOFAR SPA | |||||||||||||
Full Title: Efficacy of mesalazine in the long term prevention of diverticulitis relapses. Randomised study, double blind, controlled vs placebo. | |||||||||||||
Medical condition: Prevention of diverticulitis relapses | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000166-13 | Sponsor Protocol Number: 24-02 | Start Date: 2005-05-12 | |||||||||||
Sponsor Name: International Breast Cancer Study Group (IBCSG) | |||||||||||||
Full Title: A phase III trial evaluating the role of ovarian function suppression and the role of exemestane as adjuvant therapies for premenopausal women with endocrine responsive breast cancer. | |||||||||||||
Medical condition: Histologically proven, resected breast cancer with ER and/or PgR positive tumors | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DK (Ongoing) SE (Ongoing) DE (Completed) ES (Ongoing) IE (Ongoing) HU (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000171-18 | Sponsor Protocol Number: 3066A2-214-WW | Start Date: 2005-05-12 | ||||||
Sponsor Name: Wyeth Research Division of Wyeth Pharmaceuticals Inc. Clinical Research and Development | ||||||||
Full Title: A Multi-center, Open-label Extension Study of the Safety and Tolerability of Long-term Administration of Oral CCI-779 (Temsirolimus) in Subjects with Relapsing Multiple Sclerosis Who Completed Stud... | ||||||||
Medical condition: Multiple Sclerosis (Relapsing-remitting MS and Secondary progressive MS with relapses) | ||||||||
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Population Age: Adults | Gender: Male, Female | |||||||
Trial protocol: FI (Completed) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000360-45 | Sponsor Protocol Number: A1481222 | Start Date: 2005-05-12 | |||||||||||
Sponsor Name: PFIZER | |||||||||||||
Full Title: A MULTICENTER, PARALLEL GROUP FLEXIBLE DOSE STUDY WITH A DOUBLE BLIND, RANDOMIZED, PLACEBO CONTROLLED PHASE AND AN OPEN-LABEL PHASE TO EVALUATE THE QUALITY OF ERECTIONS IN MEN WITH ERECTILE DYSFU... | |||||||||||||
Medical condition: Erectil Dysfunction | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: IT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002399-40 | Sponsor Protocol Number: | Start Date: 2005-05-11 | ||||||
Sponsor Name: Rigshospitalet | ||||||||
Full Title: Carboplatin + paclitaxel vs carboplatin + stealth liposomal doxorubicin. A randomised multicentre trial. | ||||||||
Medical condition: Recurrent ovarian cancer Cytologic / histologic diagnosis of stage IC-IV ovarian cancer | ||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||
Trial protocol: DK (Prematurely Ended) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001019-23 | Sponsor Protocol Number: 04-TH01-01 | Start Date: 2005-05-11 | ||||||
Sponsor Name: BioInvent International AB | ||||||||
Full Title: A double blind, phase I/II, randomized, single and repeat dose, dose escalation study of the antibody BI-201 directed against Tat, given IV, versus Placebo in asymptomatic HIV-1 patients. | ||||||||
Medical condition: HIV-1 (asymptomatic patients) | ||||||||
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Population Age: Adults | Gender: Male, Female | |||||||
Trial protocol: GB (Completed) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004577-28 | Sponsor Protocol Number: MCB 0402 INT | Start Date: 2005-05-10 | |||||||||||
Sponsor Name: LEO Pharmaceutical Products Ltd. A/S (LEO Pharma A/S ) | |||||||||||||
Full Title: Different treatment regimens of calcipotriol cream and combination (calcipotiol/betamethasone dipropionate) ointment in psoriasis vulgaris | |||||||||||||
Medical condition: Psoriasis vulgaris of the trunk and/or limbs with at least 10% involvement of arms and/or 10% of legs and/or 10% of trunk | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) BE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-003742-18 | Sponsor Protocol Number: 1208.10 | Start Date: 2005-05-10 | ||||||
Sponsor Name: Boehringer Ingelheim Finland Ky | ||||||||
Full Title: A ten-week, randomized, double-blind study evaluating the efficacy of Duloxetine 60 mg once daily versus placebo in outpatients with major depressive disorder and pain (EU-Pain enriched study) | ||||||||
Medical condition: Depressed patients (according to DSM-IV criteria) experiencing painful physical symptoms | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: FI (Completed) SK (Completed) CZ (Completed) DE (Completed) | ||||||||
Trial results: View results |