- ICH GCP
- EU Clinical Trials Registry
Latest Trials
EudraCT Number: 2004-000767-10 | Sponsor Protocol Number: V82P1 | Start Date: 2004-06-29 | |||||||||||
Sponsor Name: CHIRON | |||||||||||||
Full Title: A Phase I/II, Single Center, Partially Observer-Blind, Controlled, Randomized Study to Explore Safety and Immunogenicity in Healthy Adult Subjects who Receive Either One Dose of Chiron Combined Men... | |||||||||||||
Medical condition: Active immnunisation for the prevention of invasive disease caused by N. Meningitidis serogroup C and H. influenzae type b | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000609-23 | Sponsor Protocol Number: BXL-6280213 | Start Date: 2004-06-25 | |||||||||||
Sponsor Name: BIOXELL SPA | |||||||||||||
Full Title: A randomized, double blind, placebo controlled, parallel-group study to determine the effect of BXL-628 in post-menopausal women with Overactive Bladder (OAB) | |||||||||||||
Medical condition: overactive bladder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000206-31 | Sponsor Protocol Number: C1 1304-01 | Start Date: 2004-06-22 | |||||||||||
Sponsor Name: PHARMING TECHNOLOGIES B.V. | |||||||||||||
Full Title: A randomized, placebo-controlled, double-blind Phase III study of the efficacy and safety of recombinant human C1 inhibitor for the treatment of acute attacks in patients with hereditary angioedema | |||||||||||||
Medical condition: hereditary angioedema (HAE) treatment | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) GB (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001301-10 | Sponsor Protocol Number: EOP1009 | Start Date: 2004-06-14 | |||||||||||
Sponsor Name: PFIZER | |||||||||||||
Full Title: A PHASE II PROSPECTIVE, RANDOMIZED, DOUBLE-MASKED, SHAM-CONTROLLED, DOSE-RANGING, MULTI-CENTER TRIAL TO ASSESS THE EFFECT OF PEGAPTANIB SODIUM ON FOVEAL THICKENING IN PATIENTS WITH EXUDATIVE SUBFOV... | |||||||||||||
Medical condition: AGE-RELATED MACULAR DEGENERATION | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000603-18 | Sponsor Protocol Number: Q10DOWN | Start Date: 2004-06-11 | ||||||
Sponsor Name: AZIENDA OSPEDALIERA UMBERTO I | ||||||||
Full Title: ubiquinone in Down syndrome | ||||||||
Medical condition: Down syndrome | ||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||
Trial protocol: IT (Completed) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000507-17 | Sponsor Protocol Number: SC1-04 | Start Date: 2004-06-10 | ||||||
Sponsor Name: FONDAZIONE SANTA LUCIA | ||||||||
Full Title: Effectiveness of rivastigmine treatment in post-stroke patients with right brain damage and unilateral spatial neglect | ||||||||
Medical condition: Improvement of unilateral spatial neglect and functional status in right brain damaged patients | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: IT (Ongoing) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000782-35 | Sponsor Protocol Number: CERL080AIT06 | Start Date: 2004-06-10 | |||||||||||
Sponsor Name: NOVARTIS FARMA | |||||||||||||
Full Title: EVALUATION OF THE QUALITY OF LIFE AND GASTROINTESTINAL SYMPTOMS AFTER CONVERSION TO MYFORTIC (ERL080) and CELLCEPT WITHDRAWAL IN MAINTENANCE RENAL TRANSPLANT RECIPIENTS TREATED WITH TACROLIMUS. | |||||||||||||
Medical condition: Prophylaxis of transplant rejection in adult patients receiving calcineurin inhibitors with / without corticosteroids after allogeneic renal transplants. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000374-31 | Sponsor Protocol Number: SB-683699/003 | Start Date: 2004-06-09 | ||||||
Sponsor Name: GLAXO SMITHKLINE | ||||||||
Full Title: A Randomised, Double-blind, Placebo-controlled, Parallel Group, Dose-Ranging Study to Investigate the Efficacy and Safety of Three Months administration of SB 683699 (150 - 1200mg twice daily) in ... | ||||||||
Medical condition: Relapsing Multiple Sclerosis | ||||||||
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Population Age: Adults | Gender: Male, Female | |||||||
Trial protocol: IT (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2009-017840-15 | Sponsor Protocol Number: KS-2003-06 | Start Date: 2004-05-31 | ||||||
Sponsor Name: DSC Services, s.r.o. | ||||||||
Full Title: Srovnání účinnosti kapecitabinu (Xeloda) s kontinuálním podáním 5-fluorouracilu v předoperační konkomitantní léčbě s radioterapií u karcinomu rekta | ||||||||
Medical condition: Rectal cancer stage II and III | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: CZ (Completed) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000376-14 | Sponsor Protocol Number: CLAF237A2309 | Start Date: 2004-05-28 | |||||||||||
Sponsor Name: NOVARTIS FARMA | |||||||||||||
Full Title: A MULTICENTER, RANDOMIZED, DOUBLE-BLIND, ACTIVE CONTROLLED STUDY TO COMPARE THE EFFECT OF 52 WEEKS TREATMENT WITH LAF237 50 MG BID TO METFORMIN UP TO 1000 MG BID IN DRUG NAIVE PATIENTS WITH TYPE 2 ... | |||||||||||||
Medical condition: MONOTHERAPY TREATMENT OF PATIENTS WITH TYPE 2 DIABETES | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |