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EudraCT Number: 2004-000518-37 | Sponsor Protocol Number: 580299/013 | Start Date: 2004-08-27 | ||||||
Sponsor Name: GlaxoSmithKline AS | ||||||||
Full Title: A phase III, double-blind, randomized, controlled study to evaluate the safety and immunogenicity of GlaxoSmithKline Biologicals’ HPV-16/18 VLP/AS04 vaccine administered intramuscularly according t... | ||||||||
Medical condition: cervical cancer: the study is conducted in healthy female adolescents | ||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Female | |||||||
Trial protocol: NO (Completed) ES (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-000909-22 | Sponsor Protocol Number: MDS-KET-2004-01 | Start Date: 2004-08-27 | ||||||
Sponsor Name: MDS Pharma Services | ||||||||
Full Title: Comparative efficacy and tolerability of a topical ketoprofen TDS patch vs ketoprofen gel in the treatment of acute pain in soft-tissue injuries | ||||||||
Medical condition: Acute pain in soft-tissue injuries of lower limbs, except toes | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: ES (Ongoing) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000440-24 | Sponsor Protocol Number: SDX-101-03 | Start Date: 2004-08-24 | ||||||
Sponsor Name: Cephalon UK Limited | ||||||||
Full Title: A Randomized, Multi-Center, Phase II Study to Investigate the Safety and Efficacy of SDX-101 (R-etodolac) in Combination with Chlorambucil, and that of Chlorambucil alone, in Patients with Chronic ... | ||||||||
Medical condition: Chronic Lymphocytic Leukemia (CLL) | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: SE (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-001175-19 | Sponsor Protocol Number: 102247 | Start Date: 2004-08-24 | ||||||
Sponsor Name: GlaxoSmithKline | ||||||||
Full Title: A phase IIIb, double-blind, randomized, placebo-controlled, multi-country and multi-center study to assess the efficacy, safety and immunogenicity of two doses of GSK Biologicals’ oral live attenua... | ||||||||
Medical condition: Two-dose immunization according to 0, 1 or 2-month schedule against rotavirus disease in healthy infants aged 6 to 14 weeks at the time of the first dose. Rotavirus infection. | ||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |||||||
Trial protocol: FI (Completed) CZ (Completed) IT (Completed) ES (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-000752-17 | Sponsor Protocol Number: WO17299 | Start Date: 2004-08-24 | |||||||||||
Sponsor Name: Hoffmann-La Roche Ltd/Inc/AG/Roche Global Development | |||||||||||||
Full Title: Phase II study of Herceptin® alone or in combination with a taxane, as a first-line treatment for patients with metastatic breast cancer, who have relapsed after receiving Herceptin® in the adjuvan... | |||||||||||||
Medical condition: Metastatic breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: HU (Completed) ES (Completed) AT (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000088-92 | Sponsor Protocol Number: F7CBI-1600 | Start Date: 2004-08-23 | |||||||||||
Sponsor Name: Novo Nordisk A/S | |||||||||||||
Full Title: A Randomised, Double-Blind, Placebo-Controlled, Multi-centre, Dose Escalation Study to Evaluate the Safety and Preliminary Efficacy of Recombinant Factor VIIa (NovoSeven®/Niastase®) with Brain Cont... | |||||||||||||
Medical condition: Contusive Brain Injury | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001098-25 | Sponsor Protocol Number: NAC-E-21 | Start Date: 2004-08-23 | ||||||
Sponsor Name: Zambon SA | ||||||||
Full Title: N-Acetylcisteine (NAC) effect on the inmunologycal system | ||||||||
Medical condition: Postmenopausal health woman aged more than 50 years | ||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||
Trial protocol: ES (Completed) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001103-35 | Sponsor Protocol Number: NSGO -EC - 0302 | Start Date: 2004-08-20 | ||||||
Sponsor Name: Nordic Society for Gynecologic Oncology | ||||||||
Full Title: Exemestane in Advanced or Recurrent Endometrial Carcinoma. A multicentre non-randomized Phase II study | ||||||||
Medical condition: Advanced or recurrent endometrial carcinoma | ||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||
Trial protocol: DK (Ongoing) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001308-11 | Sponsor Protocol Number: F1D-XM-HGLW | Start Date: 2004-08-19 | |||||||||||
Sponsor Name: Lilly.S.A. | |||||||||||||
Full Title: Optimal Treatment Duration with Olanzapine following Remission of Manic or Mixed Episode. An Open-Label, Randomized Trial Comparing Two Treatment Strategies | |||||||||||||
Medical condition: to compare the efficacy in the prevention of relapse to manic, depressive, or mixed episodes in two groups of bipolar I patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000483-27 | Sponsor Protocol Number: PRA/BIA-2093-302 | Start Date: 2004-08-19 | ||||||
Sponsor Name: BIAL - Portela & Ca, S.A. | ||||||||
Full Title: Efficacy and safety of BIA 2-093 as adjunctive therapy for refractory partial seizures in a double-blind, randomised, placebo-controlled, parallel-group, multicentre clinical trial. | ||||||||
Medical condition: Refractory partial epilepsy | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: SE (Completed) ES (Completed) DK (Completed) | ||||||||
Trial results: View results |