- Trials with a EudraCT protocol (60)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (6)
60 result(s) found for: Basiliximab.
Displaying page 1 of 3.
EudraCT Number: 2006-004303-19 | Sponsor Protocol Number: BSX - 001 | Start Date*: 2007-04-25 | |||||||||||
Sponsor Name:Cerimon Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Evaluation of the Safety, Efficacy, and Pharmacokinetics of Multiple Doses of Basiliximab, with Concomitant Corticosteroids, in Steroid-Refractory Ulc... | |||||||||||||
Medical condition: Steroid-refractory ulcerative colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) CZ (Prematurely Ended) SK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012350-20 | Sponsor Protocol Number: MSC-KTx | Start Date*: 2008-01-14 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA "OSPEDALI RIUNITI DI BERGAMO" (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: MESENCHYMAL STEM CELLS UNDER BASILIXIMAB/ LOW DOSE RATG TO INDUCE RENAL TRANSPLANT TOLERANCE | |||||||||||||
Medical condition: Patients will be those receiving a living-related kidney transplant | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006319-54 | Sponsor Protocol Number: BSX-002 | Start Date*: 2007-04-25 | |||||||||||
Sponsor Name:Cerimon Pharmaceuticals, Inc. | |||||||||||||
Full Title: An Open Label Evaluation of the Safety and Efficacy of Basiliximab Maintenance in Ulcerative Colitis | |||||||||||||
Medical condition: Steroid-refractory ulcerative colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) BE (Completed) CZ (Prematurely Ended) SK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-008553-27 | Sponsor Protocol Number: CTSU3C1 | Start Date*: 2009-12-02 | |||||||||||
Sponsor Name:University of Oxford | |||||||||||||
Full Title: Open-label, randomised multicentre study of CAMPATH-1H versus basiliximab induction treatment and sirolimus versus tacrolimus maintenance treatment for the preservation of renal function in patient... | |||||||||||||
Medical condition: Renal transplantation. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005335-83 | Sponsor Protocol Number: OUS-PTx-01 | Start Date*: 2013-04-05 | |||||||||||
Sponsor Name:Oslo University Hospital Rikshospitalet | |||||||||||||
Full Title: A Randomized Open-label Study: Efficacy and safety of basiliximab combined with tacrolimus, mycophenolate and low-dose corticosteroids vs thymoglobulin, tacrolimus, mycophenolate and high-dose co... | |||||||||||||
Medical condition: The only indication for pancreas-transplantation (PTx) is advanced and/or badly controlled diabetes mellitus. Patients who have developed renal insufficiency due do diabetic nephropathy may be cand... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000766-11 | Sponsor Protocol Number: 1248403 | Start Date*: 2013-05-21 |
Sponsor Name:CHU Toulouse | ||
Full Title: | ||
Medical condition: | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003528-29 | Sponsor Protocol Number: CCHI621ADE04 | Start Date*: 2016-04-14 | ||||||||||||||||
Sponsor Name:Novartis Pharma GmbH | ||||||||||||||||||
Full Title: A Multicenter, Open-label, Randomized, Two Arm Study to Investigate the Efficacy and Safety of a Therapy Avoiding Intraoperative Steroids in Combination With Basiliximab, Cyclosporine/Cyclosporine ... | ||||||||||||||||||
Medical condition: Liver Transplantation Infection | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: Outside EU/EEA | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-001407-11 | Sponsor Protocol Number: Certican MHH PRTx01 | Start Date*: 2006-07-18 | |||||||||||
Sponsor Name:Medizinische Hochschule Hannover | |||||||||||||
Full Title: A single center study investigating ciclosporine A microemulsion in combination with basiliximab and prednisolon and switch to low-dose ciclosporine A and everolimus without steroids in the prevent... | |||||||||||||
Medical condition: Kidney transplantation after end stage renal failure | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003189-25 | Sponsor Protocol Number: ASSTRO | Start Date*: 2011-03-29 | |||||||||||
Sponsor Name:ASOCIACION PARA LA INVESTIGACION Y TRATAMIENTO DE ENFERMEDADES RENALES (AITER), | |||||||||||||
Full Title: ensayo multicéntrico, aleatorizado, abierto que compara la eficacia y seguridad de un régimen inmunosupresor basado en basiliximab, introducción inmediata de dosis reducidas de tacrolimus de libera... | |||||||||||||
Medical condition: En casos de trasplantes renales en pacientes añosos, los injertos tienen una incidencia mayor de necrosis tubular aguda, y mayor sensibilidad a los efectos de las drogas nefrotóxicas, implicando un... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002231-32 | Sponsor Protocol Number: PMR-EC-1106 | Start Date*: 2009-03-04 | |||||||||||
Sponsor Name:Astellas Pharma Europe Ltd. | |||||||||||||
Full Title: A MULTICENTER, THREE ARM, RANDOMIZED, OPEN LABEL CLINICAL STUDY TO COMPARE RENAL FUNCTION IN LIVER TRANSPLANT RECIPIENTS RECEIVING AN IMMUNOSUPPRESSIVE REGIMEN OF ADVAGRAF® (IMMEDIATELY OR DELAYED... | |||||||||||||
Medical condition: RENAL FUNCTION IN LIVER TRANSPLANT RECIPIENTS RECEIVING AN IMMUNOSUPPRESSIVE REGIMEN OF ADVAGRAF® (IMMEDIATELY OR DELAYED POST-TRANSPLANT) AND MMF WITH OR WITHOUT SIMULECT | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) AT (Completed) HU (Completed) BE (Completed) CZ (Completed) IE (Completed) DE (Completed) FR (Completed) ES (Completed) GB (Completed) IT (Completed) SE (Completed) DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000137-39 | Sponsor Protocol Number: CRAD001HFR02 | Start Date*: 2012-04-06 |
Sponsor Name:Novartis Pharma S.A.S | ||
Full Title: | ||
Medical condition: | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-019638-28 | Sponsor Protocol Number: PMR-EC-1211 | Start Date*: 2010-11-22 | |||||||||||
Sponsor Name:Astellas Pharma Europe Ltd. | |||||||||||||
Full Title: INVESTIGATING NEW ONSET DIABETES MELLITUS IN KIDNEY TRANSPLANT RECIPIENTS RECEIVING AN ADVAGRAF-BASED IMMUNOSUPPRESSIVE REGIMEN WITH OR WITHOUT CORTICOSTEROIDS – A MULTICENTER, TWO ARM, RANDOMIZED... | |||||||||||||
Medical condition: Prophylaxis of rejection in kidney allograft recipients (by immunosuppression) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) CZ (Completed) SK (Completed) HU (Completed) ES (Completed) LV (Completed) LT (Completed) EE (Completed) NL (Completed) SE (Completed) IT (Completed) DE (Completed) PT (Completed) BE (Completed) RO (Completed) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005376-13 | Sponsor Protocol Number: PMR-EC-1210 | Start Date*: 2008-02-27 | |||||||||||
Sponsor Name:Astellas Pharma Europe Ltd. | |||||||||||||
Full Title: A MULTICENTER, FOUR ARM, RANDOMIZED, OPEN LABEL CLINICAL STUDY INVESTIGATING OPTIMIZED DOSING IN A PROGRAF®-/ ADVAGRAF®-BASED IMMUNOSUPPRESSIVE REGIMEN IN KIDNEY TRANSPLANT SUBJECTS. Protocol for P... | |||||||||||||
Medical condition: Prophylaxis of rejection in kidney allograft recipients (via immunosuppression) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) CZ (Completed) ES (Completed) HU (Completed) IE (Completed) GB (Completed) SE (Completed) NL (Completed) AT (Completed) GR (Completed) SK (Completed) PT (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002293-39 | Sponsor Protocol Number: BIOIMMUN | Start Date*: 2017-10-10 | |||||||||||
Sponsor Name:ORIOL BESTARD | |||||||||||||
Full Title: MULTICENTER, RANDOMIZED STUDY, TO EVALUATE THE EFFECTIVENESS OF INDIVIDUALIZATION OF IMMUNOLOGICAL RISK BASED ON SELECTIVE BIOMARKERS (DISPARITY OF HLA EPLETS AND ELISPOT-γ) TO OPTIMIZE IMMUNOSUPPR... | |||||||||||||
Medical condition: PROPHYLAXIS OF REJECTION AFTER KIDNEY TRANSPLANTATION | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-008754-23 | Sponsor Protocol Number: CILT08 | Start Date*: 2009-12-16 | ||||||||||||||||||||||||||
Sponsor Name:University Medical Center Göttingen | ||||||||||||||||||||||||||||
Full Title: A Therapeutic Exploratory Study to Determine the Efficacy and Safety of Calcineurin-Inhibitor-Free de-novo Immunosuppression after Liver Transplantation. | ||||||||||||||||||||||||||||
Medical condition: Patients with renal dysfunction undergoing liver transplantation | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-000520-32 | Sponsor Protocol Number: FG-506-02-42 | Start Date*: 2005-01-26 | |||||||||||
Sponsor Name:Fujisawa GmbH | |||||||||||||
Full Title: A MULTICENTRE, RANDOMISED, OPEN CLINICAL STUDY TO COMPARE THE EFFICACY AND SAFETY OF A COMBINATION OF TACROLIMUS AND MYCOPHENOLATE MOFETIL BASED REGIMEN WITH OR WITHOUT INDUCTION IN ELDERLY RECIPIE... | |||||||||||||
Medical condition: Patients with end stage kidney disease who will undergo primary renal transplantion or retransplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005604-14 | Sponsor Protocol Number: AIFA TX | Start Date*: 2006-12-19 | |||||||||||
Sponsor Name:IST. DI RICERCHE FARMACOLOG. M. NEGRI | |||||||||||||
Full Title: A randomized, prospective, multicenter trial to compare the effect on chronic allograft nephropathy prevention of mycophenolate mofetil versus azathioprine as the sole immunosuppressive therapy f... | |||||||||||||
Medical condition: kidney transplant | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003298-24 | Sponsor Protocol Number: EVITAESTEROIDE-12 | Start Date*: 2014-06-26 | |||||||||||
Sponsor Name:Sociedad Andaluza de Trasplante de Órganos y Tejidos (SATOT) | |||||||||||||
Full Title: Steroid withdrawal and novo donor-specific anti-HLA antibodies in renal transplant patients: a prospective, randomized and controlled study in parallel groups. | |||||||||||||
Medical condition: Kidney transplantaion | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003195-12 | Sponsor Protocol Number: CHUBX2012/29 | Start Date*: 2013-10-01 |
Sponsor Name:CHU de Bordeaux | ||
Full Title: A multicenter, two arms, randomized, open label clinical Phase IV study investigating the proportion of CMV seropositive kidney transplant recipients who will develop a CMV infection within the fir... | ||
Medical condition: CMV infection in CMV-seropositive de novo kidney transplant recipients receiving an immunosuppressive regimen. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-021075-89 | Sponsor Protocol Number: PMR-EC-1107 | Start Date*: 2010-08-25 | |||||||||||
Sponsor Name:Astellas Pharma Europe Ltd. | |||||||||||||
Full Title: A MULTICENTER, THREE ARM, RANDOMIZED, OPEN LABEL CLINICAL STUDY TO COMPARE RENAL FUNCTION IN LIVER TRANSPLANT RECIPIENTS RECEIVING AN IMMUNOSUPPRESSIVE REGIMEN OF ADVAGRAF® (IMMEDIATELY OR DELAYED... | |||||||||||||
Medical condition: RENAL FUNCTION IN LIVER TRANSPLANT RECIPIENTS RECEIVING AN IMMUNOSUPPRESSIVE REGIMEN OF ADVAGRAF® (IMMEDIATELY OR DELAYED POST-TRANSPLANT) AND MMF WITH OR WITHOUT SIMULECT | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
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