- Trials with a EudraCT protocol (693)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
693 result(s) found for: Non Hodgkin's Lymphoma.
Displaying page 32 of 35.
| EudraCT Number: 2022-001147-24 | Sponsor Protocol Number: ONC-2021-001 | Start Date*: 2023-04-12 | |||||||||||
| Sponsor Name:IRCCS ISTITUTO CLINICO HUMANITAS | |||||||||||||
| Full Title: Use of LOncastuximab Tesirine in patients with RElapsed/Refractory Diffuse Large B-Cell LYmphoma (DLBCL) or High Grade B-Cell Lymphoma (HGBCL) who have progressive disease after CAR T-cell treatmen... | |||||||||||||
| Medical condition: Patients affected by relapsed/refractory DLBCL or HGBCL failing CAR T-cell therapy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-019587-36 | Sponsor Protocol Number: DSHNHL2009-1 | Start Date*: 2011-10-10 | |||||||||||
| Sponsor Name:Universität des Saarlandes | |||||||||||||
| Full Title: Improvement of outcome and reduction of toxicity in elderly patients with CD20+ aggressive B-cell lymphoma by an optimised schedule of the monoclonal antibody rituximab, substitution of conventiona... | |||||||||||||
| Medical condition: Diffuse large B-cell lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-001860-12 | Sponsor Protocol Number: CMAK683X2101 | Start Date*: 2017-01-26 | ||||||||||||||||
| Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
| Full Title: A phase I/II, multicenter, open-label study of MAK683 in adult patients with advanced malignancies | ||||||||||||||||||
| Medical condition: Advanced malignancies | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) FR (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2013-001265-16 | Sponsor Protocol Number: COEB071X2103 | Start Date*: 2013-09-30 |
| Sponsor Name:Novartis Farma S.p.A | ||
| Full Title: An Open-Label, Single-arm, Phase Ib/II study of AEB071 (a Protein Kinase C Inhibitor) and Everolimus (mTOR inhibitor) in Patients with CD79-mutant or ABC subtype Diffuse Large B-Cell Lymphoma | ||
| Medical condition: Diffuse Large B-cell Lymphoma (DLBCL) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: IT (Prematurely Ended) DE (Prematurely Ended) NL (Prematurely Ended) FR (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-000736-21 | Sponsor Protocol Number: HLX01-FL03 | Start Date*: 2020-07-02 | |||||||||||
| Sponsor Name:Shanghai Henlius Biotech Inc. | |||||||||||||
| Full Title: A Phase 3 Multi-Centre, Randomised, Double-Blind, Parallel-Arm Study to Evaluate the Efficacy and Safety of HLX01 Versus Rituximab (Mabthera®) as First Line Treatment in Patients With Low Tumour Bu... | |||||||||||||
| Medical condition: Low tumour burden follicular lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-013351-30 | Sponsor Protocol Number: 341 | Start Date*: 2010-01-07 |
| Sponsor Name:Universitätsmedizin der Johannes Gutenberg-Universität Mainz | ||
| Full Title: A phase I/II trail to evaluate the safety, feasibility and efficacy of the addition of temsirolimus (Torisel™) to a regimen of bendamustine and rituximab for the treatment of patients with follicul... | ||
| Medical condition: Patients with relapsed mantle cell and folicular lymphoma requiring treatment. A novel combination regimene is evaluated to evaluate the safety and feasibility (phase I) and the efficacy of an esta... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-001998-40 | Sponsor Protocol Number: GO29833 | Start Date*: 2016-03-01 | |||||||||||||||||||||
| Sponsor Name:F. HOFFMANN - LA ROCHE LTD. | |||||||||||||||||||||||
| Full Title: A PHASE Ib/II STUDY EVALUATING THE SAFETY AND EFFICACY OF OBINUTUZUMAB IN COMBINATION WITH POLATUZUMAB VEDOTIN AND VENETOCLAX IN PATIENTS WITH RELAPSED OR REFRACTORY FOLLICULAR LYMPHOMA AND RITUXIM... | |||||||||||||||||||||||
| Medical condition: Relapsed or refractory, follicular lymphoma (FL) or diffuse large B-cell lymphoma (DLBCL) | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2019-000104-15 | Sponsor Protocol Number: CCS1477-02 | Start Date*: 2021-07-29 |
| Sponsor Name:CellCentric Ltd | ||
| Full Title: An open-label Phase I/IIa study to evaluate the safety and efficacy of CCS1477 as monotherapy in patients with advanced haematological malignancies. | ||
| Medical condition: Acute Myeloid Leukaemia (AML)/high-risk Myelodysplastic Syndrome (MDS), Multiple Myeloma (MM) and Non-Hodgkin Lymphoma(NHL). | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-001727-11 | Sponsor Protocol Number: 307940 / 106-20 | Start Date*: 2006-03-17 |
| Sponsor Name:Schering AG, Global Medical Development | ||
| Full Title: A phase III, open-label, prospective, two-armed, multicenter, randomized, group sequential study to evaluate the efficacy and safety of subsequent treatment with the Zevalin (ibritumomab tiuxetan) ... | ||
| Medical condition: Diffuse large B-cell lymphoma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) FI (Prematurely Ended) GB (Prematurely Ended) AT (Prematurely Ended) SE (Prematurely Ended) IE (Prematurely Ended) BE (Completed) ES (Prematurely Ended) HU (Prematurely Ended) PT (Completed) IT (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-002492-17 | Sponsor Protocol Number: CLL-RT1 | Start Date*: 2019-11-13 | |||||||||||
| Sponsor Name:Universität zu Köln | |||||||||||||
| Full Title: A prospective, open-label, multicentre Phase-II-Trial to evaluate the efficacy and safety of zanubrutinib (BGB-3111), a BTK Inhibitor, plus tislelizumab (BGB-A317), a PD-1 Inhibitor, for treatment ... | |||||||||||||
| Medical condition: Patients with previously untreated Richter Transformation or patients who responded to up to one prior line of RT therapy | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) AT (Trial now transitioned) DK (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-001284-23 | Sponsor Protocol Number: XM22-ONC-305 | Start Date*: 2013-12-10 | |||||||||||
| Sponsor Name:Merckle GmbH | |||||||||||||
| Full Title: A randomized, phase IIIB, open-label, two-arm, multicenter, comparatiVe study on efficacy and safety of lipegfilgrastim (Lonquex, TEVA) in comparison to pegfilgrastim (Neulasta®, Amgen) in elderly ... | |||||||||||||
| Medical condition: The study population includes patients with aggressive B cell Non-Hodgkin Lymphoma (NHL) planned to receive systemic anti-cancer therapy with at least 6 cycles of R-CHOP-21, according to local stan... | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) ES (Completed) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-002891-18 | Sponsor Protocol Number: IRST100.06 | Start Date*: 2011-08-04 | |||||||||||
| Sponsor Name:ISTITUTO SCIENTIFICO ROMAGNOLO PER LO STUDIO E LA CURA DEI TUMORI | |||||||||||||
| Full Title: Receptorial radiotherapy with 177Lu DOTATATE in somatostatine receptors positive tumours, a phase II study. | |||||||||||||
| Medical condition: cancer patients | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-001546-25 | Sponsor Protocol Number: NL48960.029.14 | Start Date*: 2015-01-06 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:VU University Medical Center | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: Short versus extended antibiotic treatment with a carbapenem for high-risk febrile neutropenia in hematology patients with Fever of Unknown Origin: a randomized multicenter open-label non-inferiori... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Febrile neutropenia | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: NL (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2010-022293-14 | Sponsor Protocol Number: ANRS146OPTIMAL | Start Date*: 2012-08-22 |
| Sponsor Name:Inserm-ANRS | ||
| Full Title: Optimized Phase III Trial of Immuno-stimulation with Maraviroc, a CCR5 antagonist, combined with Anti Retroviral Therapy (cART) in advanced, Late diagnosed HIV-1 infected patients with an AIDS-defi... | ||
| Medical condition: HIV infection | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Completed) IT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-007827-14 | Sponsor Protocol Number: PALO-08-09 | Start Date*: 2009-11-24 | |||||||||||
| Sponsor Name:Helsinn Healthcare SA | |||||||||||||
| Full Title: Multicenter, Phase IV, Open-Label, Uncontrolled Study to Assess the Efficacy and Safety of a Single Intravenous Dose of Palonosetron 0.25 mg (Aloxi®, Onicit®, Paloxi®) in the Prevention of Chemothe... | |||||||||||||
| Medical condition: Prevention of moderately emetogenic CINV in up to four repeated and consecutive single-day MEC cycles administered to patients with Non-Hodgkin’s Lymphomas. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) CZ (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-004813-26 | Sponsor Protocol Number: GCP#04.01.020/030 | Start Date*: 2016-03-14 | |||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Gamida Cell Ltd | |||||||||||||||||||||||||||||||||||||||||||
| Full Title: Long Term Follow Up for Patients who have received Allogeneic Stem Cell Transplantation of NiCord®/CordIn™, Umbilical Cord Blood-derived Ex Vivo Expanded Stem and Progenitor Cells | |||||||||||||||||||||||||||||||||||||||||||
| Medical condition: High risk haematological malignancies Hemoglobinopathies | |||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2018-002115-96 | Sponsor Protocol Number: SCC215/P002900 | Start Date*: 2021-04-23 |
| Sponsor Name:Klinikum Stuttgart, Landeshauptstadt Stuttgart gKAöR | ||
| Full Title: Optimizing MATRix as remission induction in PCNSL: De-escalated induction treatment in newly diagnosed primary CNS lymphoma – a randomized phase III trial | ||
| Medical condition: Primary diffuse large B-cell lymphoma (DLBCL) of the central nervous system is a rare disorder confined to the cerebral parenchyma, leptomeninges, eyes or spinal cord. It accounts for 4 to 6% of al... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Trial now transitioned) AT (Trial now transitioned) IT (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-004883-29 | Sponsor Protocol Number: ONC-2006-005 | Start Date*: 2008-01-15 | |||||||||||
| Sponsor Name:ISTITUTO CLINICO HUMANITAS | |||||||||||||
| Full Title: IGEV +/- Bortezomib (VelcadeTM) as induction before high dose consolidation in relapsed/ refractory Hodgkins lymphoma after first line treatment : a randomized phase II trial | |||||||||||||
| Medical condition: Hodgkins Lymphoma | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-000445-39 | Sponsor Protocol Number: BET116183 | Start Date*: 2013-12-20 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research and Development Limited | |||||||||||||
| Full Title: A phase I/II open-label, dose escalation study to investigate the safety, pharmacokinetics, pharmacodynamics and clinical activity of GSK525762 in subjects with relapsed, refractory hematologic ... | |||||||||||||
| Medical condition: Patients with relapsed and/or refractory haematological malignancies (lymphoma, leukemia, or multiple myeloma) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-001900-39 | Sponsor Protocol Number: 11/0475 | Start Date*: 2012-11-01 | |||||||||||
| Sponsor Name:University College London | |||||||||||||
| Full Title: A multicentre randomised phase II clinical trial of Inotuzumab Ozogamicin plus Rituximab and CVP (IO-R-CVP) versus Gemcitabine plus Rituximab and CVP (Gem-R-CVP) for the first line treatment of pat... | |||||||||||||
| Medical condition: Diffuse large B cell lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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