- Trials with a EudraCT protocol (130)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
130 result(s) found for: EBV.
Displaying page 1 of 7.
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: 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: 2020-000085-42 | Sponsor Protocol Number: LLB-2019-03 | Start Date*: Information not available in EudraCT | ||||||||||||||||||||||||||
Sponsor Name:LABO'LIFE Belgium sprl | ||||||||||||||||||||||||||||
Full Title: Randomized, placebo-controlled, double blind study to evaluate the efficacy of 2LEBV® and 2LXFS® on asthenia in patients with an EBV infection. EBVAST Study | ||||||||||||||||||||||||||||
Medical condition: Epstein-Barr Virus infection | ||||||||||||||||||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: BE (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: 2012-004240-30 | Sponsor Protocol Number: AIT-MULTIVIR-01 | Start Date*: 2014-06-18 | |||||||||||
Sponsor Name:Universitätsklinikum Erlangen | |||||||||||||
Full Title: Prospective, open-label, randomised, two-arm, controlled, multicentre clinical trial, phase I/IIa, for the evaluation of safety and efficacy of an adoptive immunotherapy with allogeneic CMV-/EBV-sp... | |||||||||||||
Medical condition: Immune deficiency after allogeneic stem cell transplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000169-19 | Sponsor Protocol Number: | Start Date*: 2019-09-03 | ||||||||||||||||
Sponsor Name:Queen Mary University London | ||||||||||||||||||
Full Title: Clinical trial to determine the effect of Famciclovir on Epstein-Barr virus activity as measured by EBV shedding in saliva of patients with Multiple Sclerosis. | ||||||||||||||||||
Medical condition: Epstein Barr virus infection in people with multiple sclerosis. | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-000853-29 | Sponsor Protocol Number: TRACE | Start Date*: 2020-01-14 | ||||||||||||||||||||||||||
Sponsor Name:Klinikum der Universität München | ||||||||||||||||||||||||||||
Full Title: Treatment of chemo-refractory viral infections after allogeneic stem cell transplantation with multispecific T cells against CMV, EBV and AdV: A phase III, prospective, multicentre clinical trial | ||||||||||||||||||||||||||||
Medical condition: Chemo-refactory AdV, CMV and EBV infections after allogeneic stem cell transplantation | ||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) FR (Trial now transitioned) BE (Trial now transitioned) IT (Trial now transitioned) ES (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005105-27 | Sponsor Protocol Number: P-105-202 | Start Date*: 2022-05-02 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:AlloVir, Inc. | ||||||||||||||||||||||||||||||||||||||
Full Title: Phase 2/3, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Assess the Safety and Efficacy of ALVR105 (Viralym-M) Compared to Placebo for the Prevention of AdV, BKV, CMV, EBV, HHV... | ||||||||||||||||||||||||||||||||||||||
Medical condition: Adenovirus (AdV), BK virus (BKV), John Cunningham virus (JCV), human herpesvirus 6 (HHV- 6), Epstein-Barr virus (EBV), and cytomegalovirus (CMV) infections and/or disease in patients at high risk f... | ||||||||||||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: IT (Prematurely Ended) FR (Completed) ES (Prematurely Ended) BE (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-000763-45 | Sponsor Protocol Number: P-105-401 | Start Date*: 2022-07-25 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:AlloVir, Inc. | ||||||||||||||||||||||||||||||||||||||
Full Title: Global Registry for Long-Term Follow-up of Patients Participating in Clinical Trials with Posoleucel (ALVR105) | ||||||||||||||||||||||||||||||||||||||
Medical condition: Adenovirus (AdV), BK virus (BKV), John Cunningham virus (JCV), human herpesvirus 6 (HHV- 6), Epstein-Barr virus (EBV), and cytomegalovirus (CMV) infections and/or disease in patients at high risk f... | ||||||||||||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: IT (Prematurely Ended) ES (Ongoing) SE (Prematurely Ended) BE (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-007612-29 | Sponsor Protocol Number: UCL/09/0050 | Start Date*: 2013-02-26 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: Immunotherapy with CD19ζ chimeric antigen receptor gene-modified EBV-specific CTLs after stem cell transplant in children with high-risk acute lymphoblastic leukaemia | |||||||||||||
Medical condition: The medical condition under investigation is childhood precursor B acute lymphoblastic leukaemia (ALL). | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004725-23 | Sponsor Protocol Number: Penta-STs-001 | Start Date*: 2021-10-05 |
Sponsor Name:Γενικό Νοσοκομείο Θεσσαλονίκης "Γεώργιος Παπανικολάου" | ||
Full Title: Administration of rapidly generated multipathogen-specific T-Lymphocytes for the Treatment of AdV, CMV, EBV, BKV and Aspergillus fumigatus infections post Allogeneic Stem Cell Transplant | ||
Medical condition: Hematopoietic stem cell transplant (HSCT) recipients with AdV, EBV, CMV, BKV or Aspergillus fumigatus (AF) infection/ reactivation or with active disease. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-005017-31 | Sponsor Protocol Number: DERN | Start Date*: 2019-01-29 | |||||||||||
Sponsor Name:G.O.N.O. - GRUPPO ONCOLOGICO DEL NORD OVEST | |||||||||||||
Full Title: DENOSUMAB IN EBV RELATED NASOPHARYNGEAL CARCINOMA (NPC) AS A MODEL FOR RANK-MEDIATED IMMUNOLOGIC MODULATION OF VIRUS-RELATED TUMOURS – DERN STUDY | |||||||||||||
Medical condition: advanced or metastatic Nose Pharynx Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004817-98 | Sponsor Protocol Number: Tri-VSTs | Start Date*: 2019-06-25 |
Sponsor Name:Ελληνική Αιματολογική Εταιρεία | ||
Full Title: Administration of Rapidly Generated Multivirus-Specific Cytotoxic TLymphocytes for the Treatment of CMV, EBV, and BK virus Infections post Allogeneic Stem Cell Transplant | ||
Medical condition: Infections from EBV, CMV and BK virus post allogeneic Stem Cell Transplant | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GR (Completed) | ||
Trial results: (No results available) |
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: 2010-022444-20 | Sponsor Protocol Number: 40-41200-98-9069 | Start Date*: 2010-11-15 |
Sponsor Name:ZonMW | ||
Full Title: PHASE I-II STUDY OF GEMCITABINE AND VALPROIC ACID PLUS VALGANCICLOVIR IN PATIENTS WITH ADVANCED NASOPHARYNGEAL CARCINOMA | ||
Medical condition: Patient has histological confirmed residual, recurrent or metastatic EBV-positive Nasopharynx carcinoma that has failed conventional curative treatments and deemed incurable, or patient refuses fur... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (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: 2020-004957-62 | Sponsor Protocol Number: ET20-093 | Start Date*: 2021-09-09 |
Sponsor Name:Centre Léon Bérard | ||
Full Title: Immunotherapy in MSI/dMMR Tumors in perioperative setting | ||
Medical condition: MSI/dMMR tumors or EBV+ gastric cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
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: 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: 2013-004380-31 | Sponsor Protocol Number: CM-2013-01 | Start Date*: 2015-01-22 | |||||||||||
Sponsor Name:Cell Medica Inc. | |||||||||||||
Full Title: A Phase 2 open label study to investigate the efficacy of autologous EBV-specific T-cells for the treatment of patients with aggressive extranodal NK/T-cell lymphoma (ENKTCL). | |||||||||||||
Medical condition: Aggressive EBV positive extranodal NK/T-cell lymphoma (ENKTCL) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
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