- Trials with a EudraCT protocol (292)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
292 result(s) found for: Lymphomas non-Hodgkin's B-cell.
Displaying page 1 of 15.
| EudraCT Number: 2008-000434-47 | Sponsor Protocol Number: IM-T-hA20-08 | Start Date*: 2008-07-22 | ||||||||||||||||
| Sponsor Name:Immunomedics, Inc. | ||||||||||||||||||
| Full Title: A Phase I/II Study of Immunotherapy with Subcutaneous Administered Veltuzumab (hA20) in Patients with CD20+ Non-Hodgkin's Lymphoma or Chronic Lyphocytic Leukemia | ||||||||||||||||||
| Medical condition: Non-Hodgkin's Lymphoma and Chronic Lymphocytic Leukemia | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2007-001666-32 | Sponsor Protocol Number: APM4083g | Start Date*: 2007-12-05 | |||||||||||
| Sponsor Name:Genentech Inc | |||||||||||||
| Full Title: A PHASE II, SINGLE-ARM, OPEN-LABEL STUDY OF THE SAFETY,PHARMACOKINETICS, AND EFFICACY OF MULTIPLE DOSES OF APOMAB ADMINISTERED INTRAVENOUSLY IN COMBINATION WITH RITUXIMAB IN PATIENTS WITH FOLLICULA... | |||||||||||||
| Medical condition: Follicular, CD20-Positive B-Cell Non-Hodgkin's Lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Prematurely Ended) BE (Completed) GB (Prematurely Ended) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-004908-37 | Sponsor Protocol Number: IRIS | Start Date*: 2011-10-21 | |||||||||||
| Sponsor Name:FONDAZIONE CENTRO S. RAFFAELE DEL MONTE TABOR | |||||||||||||
| Full Title: Phase II study on activity and tolerability of intralesional rituximab in relapsed or refractory patients affected by indolentCD-20 positive lymphoma of conjuntiva; evaluation of activity of adding... | |||||||||||||
| Medical condition: indolent CD-20 positive lymphoma of conjunctiva | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-007799-40 | Sponsor Protocol Number: 2021/07 | Start Date*: 2008-01-28 | |||||||||||
| Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
| Full Title: Evaluation of intralesional administration of rituximab for treatment of orbital lymphoma | |||||||||||||
| Medical condition: orbital lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-002251-26 | Sponsor Protocol Number: CL1-078454-018 | Start Date*: 2014-09-08 | |||||||||||||||||||||
| Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||||||||||||
| Full Title: Long-term safety study of abexinostat (S 078454) per os given as single-agent in haematological malignancies – Extension study | |||||||||||||||||||||||
| Medical condition: Hodgkin's Disease (HD) , Non-Hodgkin Lymphoma (NHL) and Chronic Lymphocytic Leukaemia (CLL) | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: BE (Prematurely Ended) HU (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2013-003749-40 | Sponsor Protocol Number: GO27878 | Start Date*: 2014-07-07 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:F. Hoffmann- La Roche Ltd. | ||||||||||||||||||||||||||||||||||||||
| Full Title: A Phase Ib/II, open label study evaluating the safety and pharmacokinetics of GDC-0199 (ABT-199) in combination with Rituximab (R) or Obinutuzumab (G) plus cyclophosphamide, doxorubicin, vincristin... | ||||||||||||||||||||||||||||||||||||||
| Medical condition: B-cell non-hodgkin's lymphoma (NHL) and diffuse large B-cell lymphoma (DLBCL) | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: FR (Completed) NL (Completed) HU (Completed) CZ (Completed) ES (Completed) AT (Completed) | ||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2019-002666-12 | Sponsor Protocol Number: CJBH492A12101 | Start Date*: 2020-08-03 | ||||||||||||||||
| Sponsor Name:Novartis Pharma AG | ||||||||||||||||||
| Full Title: A phase I/Ib open-label, multi-center dose escalation study of JBH492 in patients with relapsed/refractory chronic lymphocytic leukemia (CLL) and Non Hodgkin’s Lymphoma (NHL) | ||||||||||||||||||
| Medical condition: Non-Hodgkins Lymphoma Chronic Lymphocytic Leukemia | ||||||||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FI (Prematurely Ended) DE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2012-005378-73 | Sponsor Protocol Number: TBF2012 | Start Date*: 2013-01-29 | |||||||||||
| Sponsor Name:FONDAZIONE NEOPLASIE SANGUE ONLUS | |||||||||||||
| Full Title: Allogeneic Transplantation after a Conditioning with Thiotepa, Busulfan and Fludarabin for the treatment of refractory/early relapsed aggressive B-cell non Hodgkin lymphomas: a Phase II Multi-Cente... | |||||||||||||
| Medical condition: Refractory/early relapsed aggressive B-cell non Hodgkin lymphomas | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-002339-44 | Sponsor Protocol Number: IGM-2323-001 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:IGM Biosciences, Inc. | |||||||||||||
| Full Title: A Phase 1/2 Open-Label, Multicenter Study Evaluating the Safety and Pharmacokinetics of Escalating Doses of IGM-2323 in Subjects with Relapsed/Refractory Non-Hodgkin Lymphomas | |||||||||||||
| Medical condition: Relapsed/Refractory (R/R) Non-Hodgkin lymphomas (NHL) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) ES (Completed) IT (Completed) DK (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-002989-33 | Sponsor Protocol Number: COLPRIT-0000-BAS-0041-I | Start Date*: 2023-06-29 | |||||||||||
| Sponsor Name:Klinikum rechts der Isar der Technischen Universität München | |||||||||||||
| Full Title: CHEMOKINE RECEPTOR CXCR4-DIRECTED THERANOSTICS OF ADVANCED LYMPHOPROLIFERATIVE CANCERS BY RADIOPEPTIDE-BASED IMAGING AND THERAPY: THE COLPRIT PHASE I/II STUDY | |||||||||||||
| Medical condition: Indication: Non-Hodgkin lymphomas (NHL) Advanced lymphoproliferative cancers: aggressive B- and T- cell Non-Hodgkin lymphomas (NHL), including heavily pretreated transformed indolent lymphoma (tNHL... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-003657-87 | Sponsor Protocol Number: BCNHL | Start Date*: 2007-09-14 | |||||||||||
| Sponsor Name:ISTITUTO NAZIONALE PER LA CURA TUMORI | |||||||||||||
| Full Title: Reduced intensity conditioning with high-dose rituximab followed by allogeneic transplantation of hematopoietic cells for the treatment of relapsed/refractory B-cell non Hodgkins lymphomas | |||||||||||||
| Medical condition: B-cell non-Hodgkin lymphomas | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-005552-33 | Sponsor Protocol Number: APO3585g | Start Date*: 2007-06-06 | |||||||||||
| Sponsor Name:Genentech Inc. | |||||||||||||
| Full Title: A PHASE Ib/II, OPEN-LABEL, MULTICENTER STUDY OF THE SAFETY, PHARMACOKINETICS, AND EFFICACY OF Apo2L/TRAIL ADMINISTERED INTRAVENOUSLY IN COMBINATION WITH RITUXIMAB TO SUBJECTS WITH FOLLICULAR AND OT... | |||||||||||||
| Medical condition: Follicular, CD20+, B-cell non-Hodgkin’s lymphoma. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) CZ (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-013691-47 | Sponsor Protocol Number: CL1-78454-001 | Start Date*: 2009-12-08 | |||||||||||||||||||||
| Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||||||||||||
| Full Title: Phase I/II dose-escalation study of oral administration of the Pan-Histone Deacetylase (HDAC) Inhibitor S 78454 in Hodgkin’s Disease, non-Hodgkin Lymphoma and Chronic Lymphocytic Leukaemia | |||||||||||||||||||||||
| Medical condition: Hodgkin's disease (HD) , non-Hodgkin lymphoma (NHL) and chronic lymphocytic Leukaemia (CLL) | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: FR (Completed) GB (Completed) BE (Completed) HU (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2006-001433-17 | Sponsor Protocol Number: Hx-CD20-405 | Start Date*: 2006-06-30 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
| Full Title: A single-arm, international, multi-center trial of HuMax-CD20, a fully human monoclonal anti-CD20 antibody, in patients with Follicular Lymphoma who are refractory to rituximab as monotherapy or in... | |||||||||||||
| Medical condition: Non-Hodgkin Follicular Lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) SE (Completed) DK (Prematurely Ended) DE (Completed) ES (Completed) NL (Completed) GB (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-003828-38 | Sponsor Protocol Number: ZEVALIN one shot LNH >60aa | Start Date*: 2008-09-01 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA OSPEDALE S. SALVATORE | |||||||||||||
| Full Title: Yttrium Y90Ibritumomab Tiutexan (Zevalin)as a consolidation treatment for patients with high grade non-Hodgkin's lymphoma aged >60 years. | |||||||||||||
| Medical condition: High grade B cell non-Hodgkin lymphoma. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-004097-26 | Sponsor Protocol Number: PCI-32765FLR2002 | Start Date*: 2013-02-05 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: An Open-label, Multicenter, Single-arm, Phase 2 Study of PCI-32765 (ibrutinib) in Subjects with Refractory Follicular Lymphoma | |||||||||||||
| Medical condition: Follicular Lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) GB (Completed) DE (Completed) ES (Completed) IT (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-005613-19 | Sponsor Protocol Number: R-COMP 14 | Start Date*: 2007-04-27 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA OSPEDALE S. SALVATORE | |||||||||||||
| Full Title: R-COMP 14 in elderly patients with high grade non-Hodgkin lymphoma | |||||||||||||
| Medical condition: Elderly patients with B non-Hodgkin lymphoma | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-016725-34 | Sponsor Protocol Number: C18083/2048 | Start Date*: 2010-05-21 | |||||||||||
| Sponsor Name:Cephalon, Inc. | |||||||||||||
| Full Title: An Open-Label Study to Evaluate the Efficacy and Safety of Treatment With Bendamustine in Combination With Ofatumumab in Previously Untreated Patients With Indolent B-Cell Non-Hodgkin’s Lymphoma (NHL) | |||||||||||||
| Medical condition: Non-Hodgkin’s Lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-001103-37 | Sponsor Protocol Number: B020999 | Start Date*: 2008-10-23 | ||||||||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | ||||||||||||||||||
| Full Title: An open-label, multicentre, non-randomised, dose-escalating phase I/II study, with a randomized phase II part, to investigate the safety and tolerability of RO5072759 given as monotherapy in patien... | ||||||||||||||||||
| Medical condition: For the phase I and II parts of the study, patients with CD20+ malignant disease for whom no therapy of higher priority is available and where treatment with an anti-CD20 antibody is deemed appropr... | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2018-002752-33 | Sponsor Protocol Number: NL.66760 | Start Date*: 2019-01-17 | ||||||||||||||||||||||||||
| Sponsor Name:VU University Medical Center | ||||||||||||||||||||||||||||
| Full Title: A phase I/II trial towards the safety and efficacy of preemptive vaccination with PD-L silenced, minor histocompatibility antigen UTA2-1 peptide-loaded Dendritic Cells after Allogeneic Stem Cell Tr... | ||||||||||||||||||||||||||||
| Medical condition: Multiple Myeloma (MM), Chronic Lymphocytic Leukemia (CLL), Non hodgkin lymphoma (any grade), Acute myeloid leukemia (AML) | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: NL (Ongoing) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
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