- ICH GCP
- EU Clinical Trials Registry
Latest Trials
EudraCT Number: 2005-002438-37 | Sponsor Protocol Number: 2005/VCC/0018(WCTU02) | Start Date: 2006-12-07 | |||||||||||
Sponsor Name: Velindre NHS Trust | |||||||||||||
Full Title: A randomised phase III clinical trial investigating the effect of FRAGMin® Added to standard Therapy In patients with lung Cancer | |||||||||||||
Medical condition: Lung cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005626-24 | Sponsor Protocol Number: 1247 | Start Date: 2006-12-07 | |||||||||||
Sponsor Name: POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: PHASE II STUDY ON PEMETREXED IN ADVANCED AND/OR RECURRENT CERVICAL CANCER | |||||||||||||
Medical condition: advanced or metastatic cervical cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004398-89 | Sponsor Protocol Number: 380104 | Start Date: 2006-12-06 | |||||||||||
Sponsor Name: Medinova AG | |||||||||||||
Full Title: Comparative Study of the Efficacy of 10 mg Dequalinium Chloride (Fluomizin®) in the Local Treatment of Bacterial Vaginosis | |||||||||||||
Medical condition: Bacterial Vaginosis | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) AT (Prematurely Ended) CZ (Completed) SK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001846-15 | Sponsor Protocol Number: CSUC-01/06 | Start Date: 2006-12-06 | ||||||
Sponsor Name: InDex Pharmaceuticals AB | ||||||||
Full Title: A placebo-controlled, randomised, double-blind, single dose proof of concept study of Kappaproct, in steroid resistant or steroid dependent patients with ulcerative colitis of mild to moderate degree | ||||||||
Medical condition: Active ulcerative colitis in steroid refractory or steroid dependent patients | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: SE (Prematurely Ended) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003901-10 | Sponsor Protocol Number: 250317BS | Start Date: 2006-12-06 | ||||||
Sponsor Name: Neosil Inc. | ||||||||
Full Title: A randomized, placebo controlled, double-blind study to evaluate the efficacy of topical formulations in male subjects with androgenetic alopecia | ||||||||
Medical condition: The study will be performed in male subjects with Norwood/Hamilton grades III - IV, androgenetic alopecia. | ||||||||
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Population Age: Adults | Gender: Male | |||||||
Trial protocol: DE (Completed) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005082-19 | Sponsor Protocol Number: RB23EZ | Start Date: 2006-12-06 | |||||||||||
Sponsor Name: Research Innovation Services, University of Nottingham | |||||||||||||
Full Title: Effect of an angiotensin receptor antagonist on cerebral blood flow, cerebral perfusion pressure, and systemic and peripheral haemodynamics in patients with recent stroke. | |||||||||||||
Medical condition: Patients who have hypertension in the context of recent stroke. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000474-42 | Sponsor Protocol Number: CL2-90652-002 | Start Date: 2006-12-06 | |||||||||||
Sponsor Name: INSTITUT DE RECHERCHES INTERNATIONALES SERVIER | |||||||||||||
Full Title: Safety and effects on blood pressure of a daily dose of 0.025 to 0.135 milligram per kilogram of S 90652, a paediatric formulation of perindopril, in hypertensive children having received S 90652 -... | |||||||||||||
Medical condition: Arterial Hypertension | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005143-28 | Sponsor Protocol Number: MED.RES.HOS.2006.03.LP | Start Date: 2006-12-06 | ||||||
Sponsor Name: Medicinsk Forskning | ||||||||
Full Title: Effects of HMG-CoA-reductase inhibition (atorvastatin) on renal sodium excretion, renal hemodynamics, tubular function and vasoactive hormones in healthy subjects under diet with normal and high so... | ||||||||
Medical condition: Healthy volunteer trial | ||||||||
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Population Age: Adults | Gender: Male, Female | |||||||
Trial protocol: DK (Completed) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003762-33 | Sponsor Protocol Number: 106481 | Start Date: 2006-12-06 | ||||||
Sponsor Name: GlaxoSmithKline Biologicals | ||||||||
Full Title: A phase IIIb, double blind, randomised, placebo–controlled, multi–country, multicentre study to assess the safety, reactogenicity and immunogenicity of two doses of GlaxoSmithKline (GSK) Biological... | ||||||||
Medical condition: Primary immunisation of pre–term infants against human rotavirus gastroenteritis (GE) | ||||||||
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Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |||||||
Trial protocol: FR (Completed) PT (Completed) ES (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2006-004815-24 | Sponsor Protocol Number: FM-MYEL-06-01 | Start Date: 2006-12-05 | |||||||||||
Sponsor Name: FONDAZIONE MICHELANGELO - AVANZAMENTO DELLO STUDIO E CURA DEI TUMORI | |||||||||||||
Full Title: Bortezomib and dexamethasone treatment before donor lymphocyte infusions for myeloma patients progressing or relapsing after allogeneic transplantation of hematopoietic cells | |||||||||||||
Medical condition: Myeloma patients progressing or relapsing after allogeneic transplantation | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |