- ICH GCP
- EU Clinical Trials Registry
Latest Trials
EudraCT Number: 2004-004231-53 | Sponsor Protocol Number: 506067 | Start Date: 2004-12-22 | ||||||
Sponsor Name: Royal Devon and Exeter NHS Foundation Trust | ||||||||
Full Title: The Effect Of Antihypertensive Treatment With Lisinopril and Labetalol on Baroreflex Sensitivity in Stroke | ||||||||
Medical condition: Stroke | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: GB (Completed) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2004-003829-28 | Sponsor Protocol Number: TAK-013/EC204 | Start Date: 2004-12-22 | |||||||||||
Sponsor Name: Takeda Europe R&D Centre Ltd | |||||||||||||
Full Title: An open-label investigation into the tolerability and pharmacokinetic / pharmacodynamic effects of sufugolix (TAK-013), at a dosage of 100mg twice-daily, during six months treatment of pre-menopaus... | |||||||||||||
Medical condition: symptomatic endometriosis | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002070-36 | Sponsor Protocol Number: GLU-005 | Start Date: 2004-12-22 | |||||||||||
Sponsor Name: Metcon Medicin AB | |||||||||||||
Full Title: Efficacy of MM005-Granulae as prophylaxis for nocturnal hypoglycemia in insulin treated Type 1 diabetic subjects. A double-blind, randomized, placebo-controlled phase II multi-center study in three... | |||||||||||||
Medical condition: Diabetes type I | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001339-41 | Sponsor Protocol Number: N01175 | Start Date: 2004-12-22 | |||||||||||
Sponsor Name: UCB S.A. Pharma Sector | |||||||||||||
Full Title: A therapeutic confirmatory, open-label, multi-center, randomized 2 parallel groups, community-based trial studying the efficacy and safety of levetiracetam (1000 to 3000 mg/day oral tablets 250-50... | |||||||||||||
Medical condition: Monotherapy in subjects with newly diagnosed epilepsy | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) FI (Completed) SE (Completed) SK (Completed) IE (Completed) CZ (Completed) GB (Completed) DE (Completed) BE (Completed) ES (Completed) IT (Completed) HU (Completed) PT (Not Authorised) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002598-21 | Sponsor Protocol Number: SP826 | Start Date: 2004-12-22 | ||||||
Sponsor Name: Schwarz Biosciences GmbH | ||||||||
Full Title: A phase 3b, open-label, multicenter, multinational trial to evaluate the effects of rotigotine transdermal patch on early morning motor impairment and sleep disorders in patients with idiopathic Pa... | ||||||||
Medical condition: Parkinson's Disease | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: AT (Completed) GB (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-000711-26 | Sponsor Protocol Number: IOM-114 | Start Date: 2004-12-22 | ||||||
Sponsor Name: Bracco Imaging S.p.A. | ||||||||
Full Title: ABDOMINAL COMPUTED TOMOGRAPHY: IOMERON®400 VS VISIPAQUE™320 ENHANCEMENT (ACTIVE). | ||||||||
Medical condition: subjects with mild to moderate renal impairment scheduled to undergo clinically-indicated IV contrast –enhanced MDCT scanning of the liver | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: AT (Completed) SE (Prematurely Ended) GB (Prematurely Ended) IT (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-002362-37 | Sponsor Protocol Number: GlaxoSmithKline, B2C101762 | Start Date: 2004-12-22 | ||||||
Sponsor Name: GlaxoSmithKline Research & Development Limited | ||||||||
Full Title: A multicentre, randomised, double-blind, placebo-controlled, dose ascending, four way crossover study to examine efficacy (FEV1),safety, tolerability, pharmacodynamics and pharmacokinetics of sing... | ||||||||
Medical condition: GW642444 is a new potent and selective inhaled beta-2-receptor agonist, which is being developed for once daily treatment of asthma and COPD. | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: SE (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-004230-14 | Sponsor Protocol Number: Clin-AGI001-002 | Start Date: 2004-12-22 | |||||||||||
Sponsor Name: AGI Therapeutics Limited | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled study of AGI 001 in the treatment of irritable bowel syndrome. | |||||||||||||
Medical condition: Irritable Bowel Syndrome | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000712-42 | Sponsor Protocol Number: IOM-115 | Start Date: 2004-12-22 | ||||||
Sponsor Name: Bracco Imaging S.p.A. | ||||||||
Full Title: Enhacement of the lower extremities computed tomography: IOMERON®-400 VS VISIPAQUE™-320 (ELECTIV). | ||||||||
Medical condition: subjects with mild to moderate renal impairment (SCr =1.5-2.5 mg/dL and/or calculated CrCl = 10-60 mL/min) who undergo clinically-indicated IV contrast-enhanced MDCTA scanning of the lower extremit... | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: AT (Completed) SE (Completed) GB (Prematurely Ended) IT (Prematurely Ended) | ||||||||
Trial results: View results |
EudraCT Number: 2004-003847-37 | Sponsor Protocol Number: REM 04 15 | Start Date: 2004-12-21 | |||||||||||
Sponsor Name: BIOPROJET | |||||||||||||
Full Title: An Open label uncontrolled study of the safety and efficacy of chronic intravenous Remodulin in patients with pulmonary Arterial Hypertension | |||||||||||||
Medical condition: Pulmonary Arterial Hypertension | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |