- Trials with a EudraCT protocol (1,347)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (164)
1,347 result(s) found for: Lymphoma.
Displaying page 7 of 68.
| EudraCT Number: 2015-005688-18 | Sponsor Protocol Number: Paw1 | Start Date*: 2016-05-25 | |||||||||||
| Sponsor Name:Department of Hematology, Aalborg University Hospital | |||||||||||||
| Full Title: A randomized controlled trial of alendronate as preventive treatment against the development of gluco-corticoid-induced osteoporosis in patients being treated for malignant lymphoma | |||||||||||||
| Medical condition: Age ≥ 18 years. Patients with new diagnosis or recurrence of lymphoma, which is expected to be treated with one of the listed chemotherapy regimens. Expected lifespan ≥2 years | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-002654-21 | Sponsor Protocol Number: RHMCAN1219 | Start Date*: 2017-11-23 | |||||||||||
| Sponsor Name:University Hospital Southampton NHS Foundation Trust | |||||||||||||
| Full Title: A PHASE II STUDY OF ATEZOLIZUMAB WITH RITUXIMAB, GEMCITABINE AND OXALIPLATIN IN PATIENTS WITH RELAPSED OR REFRACTORY DIFFUSE LARGE B-CELL LYMPHOMA WHO ARE NOT CANDIDATES FOR HIGH-DOSE THERAPY. | |||||||||||||
| Medical condition: Diffuse large B-cell lymphoma (most common type of non-Hodgkins lymphoma) | |||||||||||||
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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: View results | |||||||||||||
| EudraCT Number: 2009-015909-39 | Sponsor Protocol Number: INT5909 | Start Date*: 2009-12-02 | |||||||||||
| Sponsor Name:ISTITUTO NAZIONALE PER LA CURA TUMORI | |||||||||||||
| Full Title: Phase I/II trial of dexamethasone, ofatumumab and bendamustine [Treanda] (DOT) as first-line treatment of mantle-cell lymphoma (MCL) in the elderly | |||||||||||||
| Medical condition: Mantle-cell lymphoma (MCL) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-003716-12 | Sponsor Protocol Number: C34004 | Start Date*: 2017-07-18 | |||||||||||
| Sponsor Name:Millennium Pharmaceuticals, Inc., a wholly owned subsidiary of Takeda Pharmaceutical Company Limited | |||||||||||||
| Full Title: Phase 2 Study of TAK-659 in Patients With Relapsed or Refractory Diffuse Large B-Cell Lymphoma After at Least 2 Prior Lines of Chemotherapy | |||||||||||||
| Medical condition: Relapsed or Refractory Diffuse Large B-Cell Lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) ES (Prematurely Ended) DE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-001955-35 | Sponsor Protocol Number: RG_11-054 | Start Date*: 2012-02-15 | |||||||||||||||||||||
| Sponsor Name:University of Birmingham | |||||||||||||||||||||||
| Full Title: Single Arm Phase II trial assessing the safety, compliance with and activity of Bezafibrate and medroxyProgesterone acetate (BaP) as non-toxic therapy against myeloid and lymphoid cancers | |||||||||||||||||||||||
| Medical condition: Acute Myeloid Leukaemia (AML), Chronic Lymphocytic Leukaemia (CLL) and B-cell Non-Hodgkins Lymphoma (BNHL) | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2008-002115-41 | Sponsor Protocol Number: ADOPEH-LINFMYO-2007 | Start Date*: 2008-08-11 | |||||||||||
| Sponsor Name:Asociación Dr. Peset para el estudio de la Hematología (ADOPEH). | |||||||||||||
| Full Title: Estudio fase II, multicéntrico para evaluar la eficacia y la seguridad de la administración del esquema COMP-14 (CICLOFOSFAMIDA, VINCRISTINA, DOXORUBICINA LIPOSÓMICA-MYOCET® Y PREDNISONA) combinad... | |||||||||||||
| Medical condition: infoma no Hodgkin B agresivo y riesgo cardiovascular | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-005473-29 | Sponsor Protocol Number: FL-OSHO/GLSG-M3-2005-01 | Start Date*: 2007-03-28 | |||||||||||
| Sponsor Name:Klinikum der Ludwig-Maximilians-Universität München, Klinikum Großhadern | |||||||||||||
| Full Title: Randomisierte Phase III-Studie zur Primärtherapie von fortgeschrittenen follikulären Lymphomen bei älteren Patienten (>65 J.) und jüngeren Patienten, die nicht für eine Hochdosistherapie mit autolo... | |||||||||||||
| Medical condition: Fortgeschrittene follikuläre Lymphome | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-003465-33 | Sponsor Protocol Number: PLRG12 | Start Date*: 2019-04-24 | ||||||||||||||||
| Sponsor Name:Polish Lymphoma Research Group - PLRG | ||||||||||||||||||
| Full Title: Acalabrutinib in CLL and MCL patients subjected to allogeneic hematopoietic stem cell transplantation (alloSCT). | ||||||||||||||||||
| Medical condition: Mantle Cell Lymmphoma (MCL) Chronic Lymphocytic Leukaemia (CLL) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: PL (Prematurely Ended) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| 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) | ||||||||||||||||||||||||||||
| 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: 2019-003983-28 | Sponsor Protocol Number: SGN35-028 | Start Date*: 2020-11-27 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:SEAGEN INC. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: A phase 2, multicenter, single-arm study of retreatment with brentuximab vedotin in subjects with relapsed or refractory classic Hodgkin lymphoma (cHL) or CD30-expressing peripheral T cell lymphoma... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: - classic Hodgkin lymphoma (cHL) - Systemic anaplastic large cell lymphoma (sALCL) - CD30-expressing peripheral T cell lymphoma (PTCL) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2019-003982-17 | Sponsor Protocol Number: SGN35-015 | Start Date*: 2020-10-21 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:SEATTLE GENETICS, INC. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: A phase 2 open-label study of brentuximab vedotin in front-line therapy of Hodgkin lymphoma (HL) and CD30-expressing peripheral T-cell lymphoma (PTCL) in older patients or patients with significant... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: • Hodgkin lymphoma (HL) • CD30-expressing peripheral T-cell lymphoma (PTCL) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2004-003801-26 | Sponsor Protocol Number: DSHNHL 2004-R4 | Start Date*: 2005-03-14 | |||||||||||||||||||||||||||||||
| Sponsor Name:Institut für anwendungsorientierte Forschung und klinische Studien gGmbH der UMG Göttingen | |||||||||||||||||||||||||||||||||
| Full Title: Offene, multizentrische, nicht-randomisierte Phase II Studie:Dosiseskalation von Zevalin und zeitnahe Applikation der Hochdosischemotherapie BEAM gefolgt von autologer Stammzelltransplantation zur ... | |||||||||||||||||||||||||||||||||
| Medical condition: Relapse / progression of aggressive Non-Hodgkin-Lymphoma | |||||||||||||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2019-004898-63 | Sponsor Protocol Number: FIL_Copa-RB | Start Date*: 2020-08-18 | |||||||||||
| Sponsor Name:FONDAZIONE ITALIANA LINFOMI ONLUS | |||||||||||||
| Full Title: Copanlisib in combination with Rituximab-Bendamustine in patients with Relapsed-Refractory Diffuse Large B-cell Lymphoma: a multicentric Phase II trial | |||||||||||||
| Medical condition: Patients with Relapsed-Refractory Diffuse Large B-cell Lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-002896-17 | Sponsor Protocol Number: ME-401-003 | Start Date*: 2019-04-08 | ||||||||||||||||
| Sponsor Name:MEI Pharma, Inc. | ||||||||||||||||||
| Full Title: Multicenter, Open-Label, Single-Arm, Phase 2 Study of Zandelisib (ME 401) in Subjects with Follicular Lymphoma or Marginal Zone Lymphoma After Failure of Two or More Prior Systemic Therapies – The ... | ||||||||||||||||||
| Medical condition: Follicular lymphoma (FL) or Marginal Zone Lymphoma (MZL) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) FR (Prematurely Ended) BE (Prematurely Ended) AT (Prematurely Ended) DE (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2020-000354-10 | Sponsor Protocol Number: CC-220-NHL-001 | Start Date*: 2020-11-23 | |||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Celgene Corporation | |||||||||||||||||||||||||||||||||||||||||||
| Full Title: A PHASE 1/2, MULTICENTER, OPEN-LABEL STUDY TO ASSESS SAFETY, PHARMACOKINETICS, AND PRELIMINARY EFFICACY OF CC-220, ALONE AND IN COMBINATION WITH AN ANTI-CD20 MONOCLONAL ANTIBODY (MAB) IN SUBJECTS W... | |||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Relapsed or refractory lymphoma including the following subtypes: Aggressive B-cell lymphoma, follicular lymphoma, marginal zone lymphoma, mantle cell lymphoma, peripheral T-cell lymphoma and class... | |||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2005-005218-19 | Sponsor Protocol Number: DSHNHL2004-3 | Start Date*: 2007-10-12 |
| Sponsor Name:German High Grade Non-Hodgkin's Lymphoma group | ||
| Full Title: Randomised Study Comparing an Immuno-Chemotherapy with 6 Cycles of the Monoclonal anti-CD20 Antibody Rituximab in Combination with 6 Cycles of Chemotherapy with CHOP (Cyclophosphamide, Doxorubicin,... | ||
| Medical condition: Patients with untreated aggressive CD20+ Non-Hodgkin’s Lymphoma aged 18 to 60 years without major accompanying diseases with IPI= 1 (all) or IPI= 0 and bulky disease (≥7.5cm | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DK (Completed) IT (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-004014-17 | Sponsor Protocol Number: FIL_GA101_DHAP | Start Date*: 2014-08-04 | |||||||||||
| Sponsor Name:Fondazione Italiana Linfomi ONLUS | |||||||||||||
| Full Title: Phase II study with Ga101-DHAP as induction therapy in relapsed/refractory Diffuse Large B-cell Lymphoma (DLBCL) patients before High-Dose chemotherapy BEAM with autologous stem cell transplantatio... | |||||||||||||
| Medical condition: Young patients with DLBCL who failed or relapsed after one previous chemotherapy regimen. | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-003712-27 | Sponsor Protocol Number: P1605-SUR-D23 | Start Date*: 2022-07-27 | |||||||||||
| Sponsor Name:IMV Inc. | |||||||||||||
| Full Title: A Phase 2b, Open-label, Multicenter, Randomized Parallel-Group, Two-Stage, Study of an Immunotherapeutic Treatment DPX-Survivac and Pembrolizumab, with and without Intermittent LowDose Cyclophospha... | |||||||||||||
| Medical condition: Relapsed/Refractory Diffuse Large B-Cell Lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) FR (Completed) PL (Completed) HU (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-003213-18 | Sponsor Protocol Number: RHMCAN1129 | Start Date*: 2017-01-13 | |||||||||||
| Sponsor Name:University Hospital Southampton NHS Foundation Trust | |||||||||||||
| Full Title: A Phase Ib/II combination trial of acalabrutinib with rituximab, cyclophosphamide, doxorubicin,vincristine and prednisolone (R-CHOP) for patients with diffuse large B-cell lymphoma (DLBCL) | |||||||||||||
| Medical condition: Diffuse large B-cell lymphomas (most common type of non-Hodgkins lymphoma) | |||||||||||||
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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: View results | |||||||||||||
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