- ICH GCP
- Registro de ensayos clínicos de la UE
Últimos ensayos
EudraCT Number: 2004-000231-29 | Sponsor Protocol Number: WV16726 | Start Date: 2004-08-12 | ||||||
Sponsor Name: Roche Products Ltd | ||||||||
Full Title: Safety and pharmacokinetics of valganciclovir syrup formulation in paediatric solid organ transplant recipients | ||||||||
Medical condition: solid organ transplants | ||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||
Trial protocol: ES (Completed) GB (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-000843-61 | Sponsor Protocol Number: 7148LBMC02 | Start Date: 2004-08-12 | |||||||||||
Sponsor Name: ZAMBON GROUP | |||||||||||||
Full Title: Efficacy and tolerability of topical Ketoprofen TDS patch KEOFIX in the treatment of traumatic painful soft-tissue injuries | |||||||||||||
Medical condition: ANKLE SPRAIN | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001325-14 | Sponsor Protocol Number: 580299/008 | Start Date: 2004-08-12 | ||||||
Sponsor Name: GlaxoSmithKline SA | ||||||||
Full Title: Estudio en fase III, doble ciego, aleatorizado, controlado, multicéntrico para evaluar la eficacia de la vacuna HPV-16/18 VLP/AS04 de GlaxoSmithKline Biologicals comparada con la vacuna antihepatit... | ||||||||
Medical condition: cervical cancer => study is conducted in healthy female | ||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | |||||||
Trial protocol: ES (Completed) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000240-25 | Sponsor Protocol Number: CSPP100A2204 | Start Date: 2004-08-12 | ||||||
Sponsor Name: Novartis Sverige AB | ||||||||
Full Title: An 8 week double-blind, multicenter, randomized, multifactorial, placebo-controlled, parallel-group study to evaluate the efficacy and safety of aliskiren administered alone and in combination with... | ||||||||
Medical condition: Treatment of essential hypertension | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: SE (Completed) FI (Completed) SK (Completed) IT (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-000138-35 | Sponsor Protocol Number: 20030216 | Start Date: 2004-08-12 | ||||||
Sponsor Name: Amgen Inc | ||||||||
Full Title: A Study to Evaluate AMG 162 in the Treatment of Postmenopausal Osteoporosis FREEDOM (Fracture REduction Evaluation of Denosumab in Osteoporosis every & Months) | ||||||||
Medical condition: Treatment of postmenopausal osteoporosis | ||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||
Trial protocol: SE (Completed) FI (Completed) LV (Completed) NO (Completed) SK (Completed) ES (Completed) AT (Completed) LT (Completed) CZ (Completed) HU (Completed) GB (Completed) DK (Completed) IT (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-001369-17 | Sponsor Protocol Number: CFEM345D2406 | Start Date: 2004-08-12 | ||||||
Sponsor Name: Novartis Farmacéutica S.A. | ||||||||
Full Title: An open-label, randomized, multicenter study to evaluate the use of Zoledronic Acid in the prevention of cancer treatment-related bone loss in postmenopausal women with ER+ and/or PgR+ breast cance... | ||||||||
Medical condition: Prevention of cancer treatment-related bone loss in postmenopausal women with ER+ and/or PgR+ breast cancer receiving Letrozole as adjuvant therapy | ||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||
Trial protocol: ES (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-000326-70 | Sponsor Protocol Number: R076477-SCH-302/702 | Start Date: 2004-08-11 | ||||||
Sponsor Name: Janssen-Cilag, Johnson & Johnson spol. s.r.o. | ||||||||
Full Title: A Randomized, 6-Week Double-Blind, Placebo-Controlled Study With an Optional 24-Week Open-Label Extension to Evaluate the Safety and Tolerability of Flexible Doses of Extended Release OROS® Paliper... | ||||||||
Medical condition: Schizophrenia | ||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||
Trial protocol: CZ (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-000798-71 | Sponsor Protocol Number: 1 | Start Date: 2004-08-11 | ||||||
Sponsor Name: Imperial College London | ||||||||
Full Title: Efficacy of Levetiracetam in Pendular Nystagmus: A Randomized, Double-blind, Placebo-controlled trial with crossover | ||||||||
Medical condition: Pendular Nystagmus from various etiology | ||||||||
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Population Age: Adults | Gender: Male, Female | |||||||
Trial protocol: GB (Prematurely Ended) | ||||||||
Trial results: View results |
EudraCT Number: 2004-000487-27 | Sponsor Protocol Number: 0663-806 | Start Date: 2004-08-10 | |||||||||||
Sponsor Name: Merck Sharp & Dohme (Sweden) AB | |||||||||||||
Full Title: A Double-Blind, Parallel-Group, 4-week Trial to Assess the Efficacy and Safety of Etoricoxib 60mg and Diclofenac 150mg in Patients with Chronic Low Back Pain | |||||||||||||
Medical condition: Chronic Low Back Pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) HU (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000414-39 | Sponsor Protocol Number: BUP4203 | Start Date: 2004-08-10 | |||||||||||
Sponsor Name: Mundipharma OY | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, parallel group, multicenter study to evaluate the long-term efficacy and safety of Norspan® versus placebo Norspan in subjects with chronic, moderate... | |||||||||||||
Medical condition: Chronic, moderate to severe osteoarthritis pain of the hip and/or knee. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) SE (Completed) | |||||||||||||
Trial results: View results |