- Trials with a EudraCT protocol (60)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
60 result(s) found for: Solid organ transplantation.
Displaying page 1 of 3.
EudraCT Number: 2018-003640-23 | Sponsor Protocol Number: IRRB/05/18 | Start Date*: 2019-05-29 | |||||||||||||||||||||
Sponsor Name:ISTITUTO MEDITERRANEO PER I TRAPIANTI E TERAPIE AD ALTA SPECIALIZZAZIONE - ISMETT | |||||||||||||||||||||||
Full Title: USE OF HEPATITIS C+ DONORS FOR SOLID ORGAN TRANSPLANTATION IN A GEOGRAPHICAL AREA WITH HCV+ ENDEMIC INFECTION AND WITH A LOW-RATE CADAVERIC ORGAN DONOR AVAILABILITY. A PHASE II OPEN, MONOCENTRIC CL... | |||||||||||||||||||||||
Medical condition: USE OF POSITIVE DONORS FOR INFECTION OF THE HEPATITIS VIRUS FOR THE TRANSPLANTATION OF SOLID ORGANS IN AN ENDEMIC AREA FOR HEPATITIS C WITH LOW RATE OF DONATIONS FROM CADAVERS: OPEN PHASE II CLINI... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012258-19 | Sponsor Protocol Number: F506-CL-0403 | Start Date*: 2011-03-09 | |||||||||||||||||||||
Sponsor Name:Astellas Pharma Europe Ltd. | |||||||||||||||||||||||
Full Title: A Multicentre, Open-label, Pharmacokinetic Study of Modigraf® (Tacrolimus granules) in de novo Paediatric Allograft Recipients.Estudio Abierto, Multicéntrico, Farmacocinético de Modigraf® (Tacróli... | |||||||||||||||||||||||
Medical condition: De novo allograft transplantation (liver, heart, kidney) in paediatric patients. Pacientes pediátricos que reciben un trasplante de aloinjerto de novo ( hígado, corazón y riñón) | |||||||||||||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Completed) GB (Completed) DE (Completed) BE (Completed) FR (Ongoing) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-003561-15 | Sponsor Protocol Number: MYSTEP1 | Start Date*: 2016-08-30 | |||||||||||
Sponsor Name:University Hospital of Tuebingen | |||||||||||||
Full Title: Safety and Tolerance of Immunomodulating Therapy with Donor-specific Mesenchymal Stem Cells in Pediatric Living-Donor Liver Transplantation | |||||||||||||
Medical condition: Side effects of life-long immunosuppressive medication account for major morbidity after pediatric liver transplantation and impair quality of life. In-vivo and in-vitro studies have shown that MSC... | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001974-27 | Sponsor Protocol Number: STOPFLU | Start Date*: 2019-10-15 | |||||||||||||||||||||
Sponsor Name:Centre Hospitalier Universitaire Vaudois (CHUV) | |||||||||||||||||||||||
Full Title: Reducing the Burden of Influenza after Solid-Organ Transplantation: the STOP-FLU trial [Swiss Trial in solid Organ transplantation on Prevention of inFLUenza] | |||||||||||||||||||||||
Medical condition: Influenza in solid organ transplant patients | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003243-21 | Sponsor Protocol Number: TRANSGRIPE 1-2 | Start Date*: 2011-10-17 | |||||||||||
Sponsor Name:Fundación Pública Andaluza Progreso y Salud | |||||||||||||
Full Title: Randomized, comparative and prospective clinical trial evaluating efficacy and safety of a dose of seasonal flu vaccine compared to two doses of vaccine for prevention of influenza in solid organ t... | |||||||||||||
Medical condition: seasonal influenza prophylaxis in trasplant receipiens | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004322-15 | Sponsor Protocol Number: V503-IC | Start Date*: 2018-02-09 | |||||||||||||||||||||||||||||||
Sponsor Name:UZ Leuven | |||||||||||||||||||||||||||||||||
Full Title: An Open-label phase III study to investigate the safety, tolerability and immunogenicity of a nine-valent human papillomavirus (HPV) vaccine (Gardasil®9) in solid organ transplant recipients and HI... | |||||||||||||||||||||||||||||||||
Medical condition: Immune response to HPV vaccination in HIV-patients and Solid Organ Transplant patients | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-012436-32 | Sponsor Protocol Number: IVIST01 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Medizinische Hochschule Hannover | |||||||||||||
Full Title: A multicenter, randomized, open-labeled study to steer immunsuppressive and antiviral therapy by measurement of virus- (CMV, ADV, HSV) specific T cells in addition to determination of trough levels... | |||||||||||||
Medical condition: After solid organ transplantation immunosuppressive treatment disrupts the individual balance between virus-replication and cellular immune response. This can lead to an elevated risk of severe vir... | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012259-21 | Sponsor Protocol Number: F506-CL-0404 | Start Date*: 2011-03-02 | |||||||||||||||||||||
Sponsor Name:Astellas Pharma Europe Ltd. | |||||||||||||||||||||||
Full Title: A Long-term, Open-label, Non-comparative Study to Evaluate the Safety and Efficacy of a Modigraf® Based Immunosuppression Regimen in Paediatric Solid Allograft Recipients.Estudio abierto, no compar... | |||||||||||||||||||||||
Medical condition: Stable paediatric allograft recipients.Pacientes estables receptores de un aloinjerto | |||||||||||||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Prematurely Ended) GB (Prematurely Ended) DE (Prematurely Ended) BE (Completed) FR (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-002784-18 | Sponsor Protocol Number: 13005 | Start Date*: 2018-07-24 | |||||||||||
Sponsor Name:Clinical Trials and Research Governance | |||||||||||||
Full Title: Safety and efficacy of Tofacitinib in ameliorating ischaemia reperfusion injury and allograft pancreatitis in solid organ transplantation – a pilot study | |||||||||||||
Medical condition: Ischaemia reperfusion injury and allograft pancreatitis. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000793-30 | Sponsor Protocol Number: PedTac | Start Date*: 2013-10-22 | ||||||||||||||||
Sponsor Name:Oslo University Hospital - Rikshospitalet | ||||||||||||||||||
Full Title: The PedTac study Development of a pediatric pharmacokinetic population model for Tacrolimus | ||||||||||||||||||
Medical condition: Solid organ transplantation | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: NO (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004479-11 | Sponsor Protocol Number: DPTLDSG-IIT-PTLD-2 | Start Date*: 2014-09-19 | |||||||||||
Sponsor Name:DIAKO Ev. Diakonie-Krankenhaus Bremen gGmbH | |||||||||||||
Full Title: Risk-stratified Sequential Treatment of Post-transplant Lymphoproliferative Disease (PTLD) With 4 Courses of Rituximab SC Followed by 4 Courses of Rituximab SC, 4 Courses of Rituximab SC Combined W... | |||||||||||||
Medical condition: Previously untreated CD20-positive lymphoproliferative disorder (PTLD) following solid organ transplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001473-25 | Sponsor Protocol Number: CRAD001A2401 | Start Date*: 2005-01-27 |
Sponsor Name:Novartis Pharmaceuticals Corporation | ||
Full Title: A facilitated access program to provide Everolimus (RAD) for maintenance for patients completing therapy in RAD trials in solid organ transplantation. | ||
Medical condition: Solid Organ Transplant - maintenace phase | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-001294-24 | Sponsor Protocol Number: ONEnTreg13 | Start Date*: 2014-11-18 | |||||||||||
Sponsor Name:Medizinischen Klinik mit Schwerpunkt Nephrologie und Internistische Intensivmedizin/Charité - Universitätsmedizin Berlin | |||||||||||||
Full Title: The ONE Study: A Unified Approach to Evaluating Cellular Immunotherapy in Solid Organ Transplantation – Natural regulatory T-cells (nTregs) Trial. | |||||||||||||
Medical condition: Kidney allograft rejection following living-donor renal transplantation. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004301-24 | Sponsor Protocol Number: ONErgt11 | Start Date*: 2012-01-05 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Free State of Bavaria, represented by the University of Regensburg, represented by Prof. Edward K. Geissler | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: The ONE Study: A Unified Approach to Evaluating Cellular Immunotherapy in Solid Organ Transplantation – Reference Group Trial | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Kidney allograft rejection following living-donor renal transplantation. | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) FR (Completed) IT (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-000690-23 | Sponsor Protocol Number: ADVL0612;NCI-07-C-0220 | Start Date*: 2012-02-29 | |||||||||||
Sponsor Name:National Institution of Health (NCI) | |||||||||||||
Full Title: A Phase I Study of Sunitinib (SU11248), an Oral Multi-Targeted Tyrosine Kinase Inhibitor, in Children with Refractory Solid Tumors | |||||||||||||
Medical condition: Paediatric solid tumours | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006002-27 | Sponsor Protocol Number: CHUBX2011/18 | Start Date*: 2012-07-31 |
Sponsor Name:CHU de Bordeaux | ||
Full Title: Multicentre trial evaluating the immunogenicity of HPV vaccination in girls on immunosuppressive therapy. | ||
Medical condition: Infection by HPV 6, 11, 16, 18 | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000999-15 | Sponsor Protocol Number: ONEmreg12 | Start Date*: 2014-02-10 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:University Hospital Regensburg | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: The ONE Study: A Unified Approach to Evaluating Cellular Immunotherapy in Solid Organ Transplantation - M reg Trial | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Kidney allograft rejection following living-donor renal transplantation. | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-003048-21 | Sponsor Protocol Number: Uni-Köln-1667 | Start Date*: 2014-03-10 | |||||||||||||||||||||||||||||||
Sponsor Name:University of Cologne | |||||||||||||||||||||||||||||||||
Full Title: CONTROLING INTESTINAL COLONIZATION OF HIGH-RISK PATIENTS WITH EXTENDED- SPECTRUM BETALACTAMASE PRODUCING ENTEROBACTERIACEAE (ESBL-E) – A RANDOMIZED TRIAL (CLEAR) | |||||||||||||||||||||||||||||||||
Medical condition: Immunocompromised patients at high risk of bloodstream infections with colonizing bacteria. | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-024247-32 | Sponsor Protocol Number: 1263-203 | Start Date*: 2012-03-09 | ||||||||||||||||
Sponsor Name:VIROPHARMA INCORPORATED | ||||||||||||||||||
Full Title: A PHASE 2, RANDOMIZED, DOSE-RANGING STUDY TO ASSESS THE SAFETY AND ANTI-CYTOMEGALOVIRUS (CMV) ACTIVITY OF MARIBAVIR VERSUS VALGANCICLOVIR FOR TREATMENT OF CMV INFECTIONS IN TRANSPLANT RECIPIENTS WH... | ||||||||||||||||||
Medical condition: CMV INFECTIONS IN TRANSPLANT RECIPIENTS | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) DE (Completed) FR (Completed) AT (Completed) ES (Completed) GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-022871-78 | Sponsor Protocol Number: 201009H1N1MHH | Start Date*: 2010-11-10 | |||||||||||
Sponsor Name:Medizinische Hochschule Hannover | |||||||||||||
Full Title: A Phase II Study to Evaluate the Immunogenicity, Safety and Tolerability of a Seasonal Influenza Vaccine including H1N1 in Immunocompromised Adults Who Have Undergone Solid Organ Transplantation or... | |||||||||||||
Medical condition: Vaccination for seasonal influenza including H1N1 of immunocompromised adults who have undergone solid organ or bone marrow transplantation and of healthy adults | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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