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EudraCT Number: 2004-000933-12 | Sponsor Protocol Number: AX-CL-10 | Start Date: 2005-02-22 | ||||||
Sponsor Name: Axonyx Inc | ||||||||
Full Title: A randomised, double-blind, placebo-controlled study to evaluate the safety and efficacy of two different doses of phenserine-tartrate in patients with probable mild to moderate Alzheimer’s disease | ||||||||
Medical condition: Alzheimers disease is caused by a loss of nerve cells in the brain, particularly in the areas associated with memory and learning. The onset of Alzheimers's also affects the levels of a certain neu... | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: ES (Ongoing) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002934-20 | Sponsor Protocol Number: M04-691 | Start Date: 2005-02-22 | ||||||
Sponsor Name: Abbott GmbH & Co. KG | ||||||||
Full Title: A Multi-Centre, Randomized, Double-Blind, Placebo-Controlled Study of the Human Anti-TNF Monoclonal Antibody Adalimumab for the Induction of Clinical Remission in Subjects with Moderate to Severe C... | ||||||||
Medical condition: Crohn's Disease | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: BE (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-002030-19 | Sponsor Protocol Number: ABCSG-24 | Start Date: 2005-02-22 | ||||||
Sponsor Name: AUSTRIAN BREAST CANCER STUDY GROUP | ||||||||
Full Title: A randomized phase III study comparing epirubicin, docetaxel and capecitabine + G-CSF to epirubicin and docetaxel + G-CSF as neoadjuvant treatment for early HER-2 negative breast cancer and compari... | ||||||||
Medical condition: early HER-2 breast cancer | ||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||
Trial protocol: AT (Completed) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001749-13 | Sponsor Protocol Number: P04071 | Start Date: 2005-02-22 | ||||||
Sponsor Name: AESCA Pharma GesmbH | ||||||||
Full Title: Randomized Phase II Study: Temozolomide (TMZ) Concomitant to Radiotherapy followed by sequential TMZ in Advanced NSCLC Patients with CNS Metastasis versus Radiotherapy alone | ||||||||
Medical condition: Patients with non small cell lung cancer (NSCLC) have a high risk of developing brain metastasis, up to 40% as evaluated in autopsy studies. These patients are often heavily symptomatic and their l... | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: AT (Prematurely Ended) | ||||||||
Trial results: View results |
EudraCT Number: 2004-000202-49 | Sponsor Protocol Number: CN138-134 | Start Date: 2005-02-22 | ||||||
Sponsor Name: Bristol-Myers Squibb International Corporation | ||||||||
Full Title: Efficacy of Aripiprazole in Combination with Valproate or Lithium in the Treatment of Mania in Patients with Bipolar I Disorder Partially Nonresponsive to Valproate or Lithium Monotherapy Revised... | ||||||||
Medical condition: Bipolar disorder | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: EE (Completed) HU (Completed) ES (Completed) IT (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2005-000728-18 | Sponsor Protocol Number: VT002 | Start Date: 2005-02-21 | |||||||||||
Sponsor Name: AISAR ASSOCIAZIONE ITALIANA PER LO STUDIO DEGLI ANTIMICROBICI E DELLE RESISTENZE | |||||||||||||
Full Title: An experiment of phase II open label about safety and Mifepristone vgx-410 anti-HIV activity on patients affected by HIV-1 | |||||||||||||
Medical condition: Anti-HIV drug | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004269-14 | Sponsor Protocol Number: A5091026 | Start Date: 2005-02-21 | |||||||||||
Sponsor Name: Pfizer AB | |||||||||||||
Full Title: Phase 3, Multi-center, double-blind, randomized, parallel group study of the efficacy, safety, and tolerability of fixed combination torcetrapib (CP-529,414)/Atorvastatin administered orally, once ... | |||||||||||||
Medical condition: Heterozygous Familial Hypercholesterolemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) IS (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002208-14 | Sponsor Protocol Number: Protocol v.1.2 30/08/04 | Start Date: 2005-02-21 | ||||||
Sponsor Name: Cardiff and Vale NHS Trust | ||||||||
Full Title: Duration of Amiodarone therapy required for new post cardiac surgery atrial fibrillation. | ||||||||
Medical condition: Atrial fibrillation following cardiac surgery. | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: GB (Prematurely Ended) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004267-30 | Sponsor Protocol Number: Gebro-III-21-10 | Start Date: 2005-02-21 | ||||||
Sponsor Name: Gebro Pharma GmbH | ||||||||
Full Title: Efficacy and Tolerability of Dexibuprofen Film coated tablets in Comparison to Ibuprofen in Children and Adolescents with Tonsillopharyngitis | ||||||||
Medical condition: Tonsillopharyngitis | ||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||
Trial protocol: DE (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-004748-27 | Sponsor Protocol Number: Acadmed CTU01/05 | Start Date: 2005-02-21 | |||||||||||
Sponsor Name: Hull and east Yorkshire Hospitals Trust, Research and Deveopment, admin porta cabin | |||||||||||||
Full Title: An 8 week, double-blind, randomised, parallel group study to investigate the effect of 20 mg Esomeprazole (Nexium) tablets Twice daily versus placebo on symptoms associated with chronic cough due ... | |||||||||||||
Medical condition: We will be using Nexium to treat gastro-oesophageal reflux and in return this will reduce reflux related cough ( a manifestation of reflux) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |