- Trials with a EudraCT protocol (20)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
20 result(s) found for: PTLD.
Displaying page 1 of 1.
EudraCT Number: 2015-005454-35 | Sponsor Protocol Number: RG_15-235 | Start Date*: 2016-09-23 | |||||||||||
Sponsor Name:University of Birmingham | |||||||||||||
Full Title: Risk-stratified sequential Treatment with Ibrutinib and Rituximab (IR) and IR-CHOP for De-novo post-transplant Lymphoproliferative disorder (PTLD) | |||||||||||||
Medical condition: Post-transplant lymphoproliferative disorder | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
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: 2017-002949-30 | Sponsor Protocol Number: ATA129-EBV-302 | Start Date*: 2020-07-17 | ||||||||||||||||
Sponsor Name:Atara Biotherapeutics, Inc. | ||||||||||||||||||
Full Title: Multicenter, Open Label, Phase 3 Study of Tabelecleucel for Solid Organ or Allogeneic Hematopoietic Cell Transplant Subjects with Epstein-Barr Virus-Associated Post-Transplant Lymphoproliferative D... | ||||||||||||||||||
Medical condition: Epstein-Barr Virus-Associated Post-Transplant Lymphoproliferative Disease | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) FR (Trial now transitioned) ES (Ongoing) AT (Trial now transitioned) BE (Trial now transitioned) IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000492-21 | Sponsor Protocol Number: 7678 | Start Date*: 2021-06-11 |
Sponsor Name:Les Hôpitaux Universitaires de Strasbourg | ||
Full Title: Multicenter randomized two arms study evaluating the efficacy of prophylactic Rituximab in adult EBV negative kidney transplant recipients on incidence of EBV primary infection and post-transplant ... | ||
Medical condition: Kidney transplantation Epstein Barr virus | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2020-000177-25 | Sponsor Protocol Number: ATA129-EBV-205 | Start Date*: 2021-01-04 | |||||||||||
Sponsor Name:Atara Biotherapeutics, Inc. | |||||||||||||
Full Title: An Open-label, Single-arm, Multicohort, Phase 2 Study to Assess the Efficacy and Safety of Tabelecleucel in Subjects with Epstein-Barr Virus-associated Diseases | |||||||||||||
Medical condition: • EBV+ primary imunodeficiency lymphoproliferative disease (LPD) • EBV+ LPD in the setting of acquired (non-congenital) immunodeficiency • EBV+ post-transplant LPD involving the central nervous ... | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) AT (Trial now transitioned) BE (Trial now transitioned) IT (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003023-20 | Sponsor Protocol Number: UCL-PLTP-002 | Start Date*: 2008-09-11 | |||||||||||
Sponsor Name:Cliniques universitaires Saint-Luc | |||||||||||||
Full Title: TACROLIMUS – DACLIZUMAB - MYCOPHENOLATE MOFETIL IMMUNE PROPHYLAXIS IN PEDIATRIC LIVER TRANSPLANTATION. An open, pilot, investigator-driven study in 20 recipients | |||||||||||||
Medical condition: Liver transplantation | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005197-10 | Sponsor Protocol Number: VT3996-202 | Start Date*: 2021-10-01 | |||||||||||
Sponsor Name:Viracta Therapeutics, Inc. | |||||||||||||
Full Title: An Open-Label, Phase 2 Trial of Nanatinostat in Combination with Valganciclovir in Patients with Epstein-Barr Virus-Positive (EBV+) Relapsed/Refractory Lymphomas (NAVAL-1) | |||||||||||||
Medical condition: Epstein-Barr Virus-Positive (EBV+) Relapsed/Refractory Lymphomas | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) FR (Trial now transitioned) IT (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003033-42 | Sponsor Protocol Number: UKER-BLZ-PH1 | Start Date*: 2013-09-12 | |||||||||||
Sponsor Name:Universitätsklinikum Erlangen | |||||||||||||
Full Title: Prospective, open-label, multicentre clinical trial, phase I/IIa, to investigate the safety and tolerability of allogeneic B-cell concentrates CD3+-depleted, CD19+-enriched, cryopreserved (single a... | |||||||||||||
Medical condition: Status post allogeneic stem cell transplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000468-26 | Sponsor Protocol Number: Rit EBV | Start Date*: 2007-01-11 | |||||||||||
Sponsor Name:OSPEDALE POLICLINICO S. MATTEO | |||||||||||||
Full Title: A phase I/II multicentre study to evaluate the safety and efficacy of rituximab (monoclonal antibody anti-CD20) for prevention and/or therapy of EBV-disease. | |||||||||||||
Medical condition: NOT AVAILABLE | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006516-31 | Sponsor Protocol Number: IT1850071 | Start Date*: 2008-06-03 |
Sponsor Name:University Hospital Freiburg, represented by the Executive Medical Director (LÄD) | ||
Full Title: Triple arm, prospective-randomised multi centre study phase IV to evaluate calcineurin inhibitor reduced, steroid free immunosuppression after renal transplantation in low-risk patients (HARMONY-St... | ||
Medical condition: One year follow-up in patients after receiving renal transplantation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-003286-26 | Sponsor Protocol Number: PCYC-1140-IM | Start Date*: 2017-04-18 | |||||||||||
Sponsor Name:Pharmacyclics LLC | |||||||||||||
Full Title: A Randomized, Double-Blind Phase 3 Study of Ibrutinib in Combination With Corticosteroids versus Placebo in Combination With Corticosteroids in Subjects with New Onset Chronic Graft Versus Host Dis... | |||||||||||||
Medical condition: Chronic Graft Versus Host Disease (cGVHD) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) DE (Completed) ES (Completed) AT (Completed) HR (Completed) IT (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012198-36 | Sponsor Protocol Number: NTx-RTx-LD-001 | Start Date*: 2010-01-12 |
Sponsor Name:Universitätsklinikum Giessen und Marburg - Standort Giessen | ||
Full Title: Einfluss von Rituximab-Induktion und Lebendspende auf Immunregulation und Viruskontrolle nach Nierentransplantation - eine prospektive Pilotstudie | ||
Medical condition: Living donor and deceased donor kidney transplantation. ABO compatible and ABO incompatible kidney transplantation. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-001822-81 | Sponsor Protocol Number: TJT1106 | Start Date*: 2011-09-06 | ||||||||||||||||
Sponsor Name:CHU-Ulg | ||||||||||||||||||
Full Title: Infusion of third-party mesenchymal stem cells after renal or liver transplantation: a phase I-II, open-label, clinical study. | ||||||||||||||||||
Medical condition: Liver failure: end-stage liver diseases, including cirrhosis, primary liver cancer, fulminant hepatic failure and numerous other metabolic or congenital hepatic diseases. Kidney failure: end-st... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000743-29 | Sponsor Protocol Number: 2142002 | Start Date*: 2009-07-02 | |||||||||||
Sponsor Name:Heads Study Group | |||||||||||||
Full Title: Treatment of patients with post-transplant lymphoproliferative disorder (PILD) with a sequential treatment consisting of anti-CD20 antibody rituximab and CHOP + GCSF chemotherapy (including first, ... | |||||||||||||
Medical condition: Post-tranplant lymphoproliferative disorder (PTLD) | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004137-27 | Sponsor Protocol Number: ScanCLAD_1.0(formerVersion_0.1) | Start Date*: 2016-05-19 |
Sponsor Name:Transplantationscentrum, Sahlgrenska Universitetssjukhuset | ||
Full Title: A Scandinavian controlled, randomized, open-label, and multi-centre study evaluating if once-daily tacrolimus or twice-daily cyclosporin, reduces the 3-year incidence of chronic lung allograft dysf... | ||
Medical condition: Recipients of primary bilateral lung transplant allograft | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) FI (Prematurely Ended) DK (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2008-003241-89 | Sponsor Protocol Number: LCP-Tacro 3002 | Start Date*: 2010-11-05 | |||||||||||
Sponsor Name:LifeCycle Pharma A/S | |||||||||||||
Full Title: A Phase 3, Double-Blind, Double-Dummy, Multi-Center, Prospective, Randomized Study of the Efficacy and Safety of LCP-Tacro™ Tablets, Once Daily, Compared to Prograf® Capsules, Twice Daily, in Combi... | |||||||||||||
Medical condition: Prevention of Acute Allograft Rejection in De Novo Adult Kidney Transplant Recipients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) SE (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002846-30 | Sponsor Protocol Number: NLG-LBC-06 | Start Date*: 2016-09-13 | |||||||||||
Sponsor Name:HUS-The Hospital District of Helsinki and Uusimaa | |||||||||||||
Full Title: BIO-CHIC-Study BIOmarker driven and dose intensified CHemoImmunotherapy with early CNS prophylaxis in patients less than 65 years with high risk diffuse large B-cell lymphoma | |||||||||||||
Medical condition: Diffuse large B-cell lymphoma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) DK (Completed) NO (Completed) SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002419-24 | Sponsor Protocol Number: RG_19-116 | Start Date*: 2020-09-23 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:The University of Birmingham | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A multi-centre phase II trial of GvHD prophylaxis following unrelated donor stem cell transplantation comparing Thymoglobulin vs. Calcineurin inhibitor or Sirolimus-based post-transplant cyclophosp... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Acute Myeloid Leukaemia, Acute lymphoblastic leukaemia, Chronic myelomonocytic leukemia, Myelodysplastic syndromes, Non-Hodgkin lymphoma, Hodgkin lymphoma, Multiple myeloma, Chronic lymphocytic leu... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000252-28 | Sponsor Protocol Number: SHCVOLT1 | Start Date*: 2009-03-13 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A Multi-Centre Prospective Controlled Trial Comparing Calcineurin Inhibitor Monotherapy With Sirolimus Monotherapy in Hepatitis C Infected Patients with Hepatic Fibrosis Following Liver Transplanta... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Patients who have undergone liver transplantation and are infected with Hepatitis C virus. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-001657-26 | Sponsor Protocol Number: KCH-BMT-07-1.0 | Start Date*: 2008-02-29 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:King's College Hospital NHS Foundation Trust | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Single Centre Phase II Pilot study of Unrelated Cord Blood Transplantation in Patients with Poor Risk Haematological Malignancies. | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: 1. Acute, chronic leukaemia or myelodysplastic syndrome for which allogeneic transplantation is considered as the best treatment option. 2. Acute lymphoblastic leukaemia (ALL) 3. Non-Hodgkin’s l... | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
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